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klinik geliştirme asistanı - clinical development assistant (istanbul) Jobs in Istanbul

klinik geliştirme asistanı - clinical development assistant (istanbul)

accounting assistant

clinical research lead

experienced clinical research associate - sponsor dedicated - türkiye Jobs in Istanbul

experienced clinical research associate - sponsor dedicated - türkiye

clinical trials assistant

Johnson & Johnson MedTech

<div>
 At Johnson &amp; Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
 
 
 
 Job Function
 
 
 
 MedTech Sales
 
 
 
 Job Sub Function
 
 
 
 Clinical Sales &ndash; Hospital/Hospital Systems (Commission)
 
 
 
 Job Category
 
 
 
 Professional
 
 
 
 All Job Posting Locations:
 
 
 
 Istanbul, Turkey
 
 
 
 Job Description
 
 
 
 Biosense Webster, Inc., a member of Johnson &amp; Johnson's Family of Companies, is recruiting for a
 
 Clinical Development Assistant
 
 to support
 
 &Idot;stanbul territory
 
 
 
 At Biosense Webster, Inc. we have one goal &mdash; to ensure those with cardiac arrhythmias can live the lives they want. This means transforming the latest advancements in electrophysiology into a suite of tools that empowers physicians with a range of treatments for the best outcomes.
 
 
 Quality products and approaches are achievable only through collaboration with the smartest minds in electrophysiology. For more than 30 years, we&rsquo;ve been the global market leader in the science and technology of cardiac arrhythmia treatment, working with thousands of electrophysiologists to identify and develop diagnostic and treatment tools. And through onsite training, online courses and our global education centers, we work together to set new standards every day.
 
 
 Learn more about Biosense Webster at www.biosensewebster.com and follow us on LinkedIn.
 
 
 
 Clinical
 
 
 
 
 As the Clinical Development Specialist, you will:
 
 
 
 <ul>
 <li>
 Provide expert clinical product and technical assistance and training to physicians and EP Lab Staff on the effective use of BWI&rsquo;s systems and catheter equipment (e.g., The CARTO&reg; System and associated software modules and RF generator) during case procedures within an assigned geography, and in a manner that leads to meeting and exceeding business goals.
 </li>
 <li>
 Educate customers on all BWI products to optimize effective usage by providing technical and clinical information and in-service trainings.
 </li>
 <li>
 Maximize customer case support capability through proper planning and scheduling techniques.
 </li>
 <li>
 Stay current on company products instructions for use (IFU), best practices and technical troubleshooting, as well as relevant scientific clinical literature and new product information.
 
 
 </li>
 </ul>
 
 Sales
 
 
 
 <ul>
 <li>
 Use consultative selling techniques to identify potential sales opportunities within the account.
 </li>
 <li>
 Creates awareness of BWI solutions and facilitates Clinical Development Manager contact with the key decision makers to drive incremental business.
 </li>
 <li>
 Drive collaboration and maintain consistent, open lines of communication across the assigned responsibilities with the local team.
 </li>
 <li>
 Develop and grow mutually beneficial customer relationships within and beyond the EP lab, including, but not limited to physicians, nurses and technicians, clinical and hospital administrators and staff.
 
 
 </li>
 </ul>
 
 Team
 
 
 
 <ul>
 <li>
 Collaborate with peers to share best practices to increase value for customers.
 </li>
 <li>
 Ensure personal and Company compliance with government, company regulations, policies, and procedures.
 </li>
 <li>
 Prioritize and appropriately respond to requests in a high-stress environment.
 </li>
 <li>
 Maintain composure and problem-solving focus during stressful interactions.
 </li>
 <li>
 Engage in diagnostic dialogue with multiple internal and external business partners and stakeholders, and formulate solutions based on dialogue and input gained during session.
 </li>
 <li>
 Provide mentoring for new BWI commercial team members as requested.
 </li>
 <li>
 Respond daily to requests by email and phone call from customers, practitioners and partners.
 </li>
 <li>
 Perform administrative work, including managing account documentation, compliance training requirements, expense reporting, and Company system input.
 </li>
 <li>
 Maintain Safe Fleet standards according to Company guidelines.
 </li>
 <li>
 Communicate business related issues or opportunities to next management level.
 </li>
 <li>
 Ensure subordinates follow all Company guidelines related to Health, Safety and Environmental practices and that all resources needed to do so are available and in good condition.
 </li>
 <li>
 Additional duties as needed
 
 
 </li>
 </ul>
 
 Qualifications
 
 
 
 <ul>
 <li>
 Required Qualifications: A minimum of a Bachelor&rsquo;s degree
 </li>
 <li>
 Located in Istanbul
 </li>
 <li>
 A valid Driver&rsquo;s License
 </li>
 <li>
 The ability to travel related to this role is required. Must be willing and able to travel up to 40% overnight nationally.
 </li>
 <li>
 Position requires sitting for extended periods of time, working in a hospital laboratory setting, attending live patient cases, and wearing protective gear (i.e. lead aprons), and willing to work variable hours to meet patient needs
 </li>
 <li>
 Clinical Support Certificate
 </li>
 <li>
 May be required to lift up to 30 kg
 
 
 </li>
 </ul>
 
 Preferred Qualifications
 
 
 
 <ul>
 <li>
 Electrophysiology/Cath Lab or EP/Cardiovascular Device Industry experience.
 </li>
 <li>
 Experience working with highly complex technical systems and/or working in a critical patient care setting.
 </li>
 <li>
 Effective and timely communicator with co-workers and all levels of patient care team.
 </li>
 <li>
 Self-starter who performs well with autonomy and can be flexible in a dynamic work environment.
 </li>
 <li>
 Problem solver who can think critically in high pressure environments.
 </li>
 <li>
 Receptive to constructive feedback and collaborates and works well in team environment.
 </li>
 <li>
 Able to take large amounts of data and translate information into actionable insights
 </li>
 <li>
 Hunger for learning and building new skills
 
 
 </li>
 </ul>
 
 Required Skills
 
 
 
 
 Preferred Skills:
 
</div>

Klinik Geliştirme Asistanı - Clinical Development Assistant (ISTANBUL)

Johnson & Johnson

<div>At Johnson &amp; Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
MedTech Sales
Job Sub Function:
Clinical Sales &ndash; Hospital/Hospital Systems (Commission)
Job Category:
Professional
All Job Posting Locations:
Edirne, Tekirda&#287;
Job Description:
Biosense Webster, Inc., a member of Johnson &amp; Johnson's Family of Companies, is recruiting for a Clinical Development Assistant to support Edirne , Canakkale &amp; Tekirdag territory
At Biosense Webster, Inc. we have one goal &mdash; to ensure those with cardiac arrhythmias can live the lives they want. This means transforming the latest advancements in electrophysiology into a suite of tools that empowers physicians with a range of treatments for the best outcomes.
Quality products and approaches are achievable only through collaboration with the smartest minds in electrophysiology. For more than 30 years, we&rsquo;ve been the global market leader in the science and technology of cardiac arrhythmia treatment, working with thousands of electrophysiologists to identify and develop diagnostic and treatment tools. And through onsite training, online courses and our global education centers, we work together to set new standards every day.
Learn more about Biosense Webster at www.biosensewebster.com and follow us on LinkedIn.
As the Clinical Development Specialist, you will:
Clinical :<ul><li>
Provide expert clinical product and technical assistance and training to physicians and EP Lab Staff on the effective use of BWI&rsquo;s systems and catheter equipment (e.g., The CARTO&reg; System and associated software modules and RF generator) during case procedures within an assigned geography, and in a manner that leads to meeting and exceeding business goals.
</li><li>Educate customers on all BWI products to optimize effective usage by providing technical and clinical information and in-service trainings.</li><li>
Maximize customer case support capability through proper planning and scheduling techniques.
</li><li>Stay current on company products instructions for use (IFU), best practices and technical troubleshooting, as well as relevant scientific clinical literature and new product information.</li></ul>
Sales :
<ul><li>Use consultative selling techniques to identify potential sales opportunities within the account.</li><li>
Creates awareness of BWI solutions and facilitates Clinical Development Manager contact with the key decision makers to drive incremental business.
</li><li>Drive collaboration and maintain consistent, open lines of communication across the assigned responsibilities with the local team.</li><li>
Develop and grow mutually beneficial customer relationships within and beyond the EP lab, including, but not limited to physicians, nurses and technicians, clinical and hospital administrators and staff.</li></ul>
Team :
<ul><li>Collaborate with peers to share best practices to increase value for customers.
</li><li>Ensure personal and Company compliance with government, company regulations, policies, and procedures.
</li><li>Prioritize and appropriately respond to requests in a high-stress environment.
</li><li>Maintain composure and problem-solving focus during stressful interactions.
</li><li>Engage in diagnostic dialogue with multiple internal and external business partners and stakeholders, and formulate solutions based on dialogue and input gained during session.
</li><li>Provide mentoring for new BWI commercial team members as requested.
</li><li>Respond daily to requests by email and phone call from customers, practitioners and partners.</li><li>
Perform administrative work, including managing account documentation, compliance training requirements, expense reporting, and Company system input.</li><li>
Maintain Safe Fleet standards according to Company guidelines.
</li><li>Communicate business related issues or opportunities to next management level.
</li><li>Ensure subordinates follow all Company guidelines related to Health, Safety and Environmental practices and that all resources needed to do so are available and in good condition.
</li><li>Additional duties as needed</li></ul>
Qualifications<ul><li>
Required Qualifications: A minimum of a Bachelor&rsquo;s degree</li><li>
Located in Edirne or Tekirdag</li><li>
A valid Driver&rsquo;s License</li><li>
The ability to travel related to this role is required. Must be willing and able to travel up to 40% overnight nationally.</li><li>
Position requires sitting for extended periods of time, working in a hospital laboratory setting, attending live patient cases, and wearing protective gear (i.e. lead aprons), and willing to work variable hours to meet patient needs</li><li>
Clinical Support Certificate</li><li>
May be required to lift up to 30 kg</li></ul>
Preferred Qualifications:<ul><li>
Electrophysiology/Cath Lab or EP/Cardiovascular Device Industry experience.
</li><li>Experience working with highly complex technical systems and/or working in a critical patient care setting.</li><li>
Effective and timely communicator with co-workers and all levels of patient care team.</li><li>
Self-starter who performs well with autonomy and can be flexible in a dynamic work environment.</li><li>
Problem solver who can think critically in high pressure environments.</li><li>
Receptive to constructive feedback and collaborates and works well in team environment.</li><li>
Able to take large amounts of data and translate information into actionable insights</li><li>
Hunger for learning and building new skills</li></ul>
Required Skills:
Preferred Skills:
Qualifications<ul><li>
Required Qualifications: A minimum of a Bachelor&rsquo;s degree</li><li>
Located in Edirne or Tekirdag</li><li>
A valid Driver&rsquo;s License</li><li>
The ability to travel related to this role is required. Must be willing and able to travel up to 40% overnight nationally.</li><li>
Position requires sitting for extended periods of time, working in a hospital laboratory setting, attending live patient cases, and wearing protective gear (i.e. lead aprons), and willing to work variable hours to meet patient needs</li><li>
Clinical Support Certificate</li><li>
May be required to lift up to 30 kg</li></ul>
Preferred Qualifications:<ul><li>
Electrophysiology/Cath Lab or EP/Cardiovascular Device Industry experience.
</li><li>Experience working with highly complex technical systems and/or working in a critical patient care setting.</li><li>
Effective and timely communicator with co-workers and all levels of patient care team.</li><li>
Self-starter who performs well with autonomy and can be flexible in a dynamic work environment.</li><li>
Problem solver who can think critically in high pressure environments.</li><li>
Receptive to constructive feedback and collaborates and works well in team environment.</li><li>
Able to take large amounts of data and translate information into actionable insights</li><li>
Hunger for learning and building new skills</li></ul></div>

Klinik Geliştirme Asistanı - Clinical Development Assistant (EDIRNE , TEKIRDAG & CANAKKALE)

<div>At Johnson &amp; Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
MedTech Sales
Job Sub Function:
Clinical Sales &ndash; Hospital/Hospital Systems (Commission)
Job Category:
Professional
All Job Posting Locations:
Rize, Trabzon
Job Description:<div><div>
Job Description</div></div><div><div><div><div><div><div><div><div><div>
Biosense Webster, Inc., a member of Johnson &amp; Johnson's Family of Companies, is recruiting for a Clinical Development Assistant to support Trabzon &amp; Rize territory
At Biosense Webster, Inc. we have one goal &mdash; to ensure those with cardiac arrhythmias can live the lives they want. This means transforming the latest advancements in electrophysiology into a suite of tools that empowers physicians with a range of treatments for the best outcomes.
Quality products and approaches are achievable only through collaboration with the smartest minds in electrophysiology. For more than 30 years, we&rsquo;ve been the global market leader in the science and technology of cardiac arrhythmia treatment, working with thousands of electrophysiologists to identify and develop diagnostic and treatment tools. And through onsite training, online courses and our global education centers, we work together to set new standards every day.
Learn more about Biosense Webster at www.biosensewebster.com and follow us on LinkedIn.
As the Clinical Development Specialist, you will:
Clinical :<ul><li>
Provide expert clinical product and technical assistance and training to physicians and EP Lab Staff on the effective use of BWI&rsquo;s systems and catheter equipment (e.g., The CARTO&reg; System and associated software modules and RF generator) during case procedures within an assigned geography, and in a manner that leads to meeting and exceeding business goals.
</li><li>Educate customers on all BWI products to optimize effective usage by providing technical and clinical information and in-service trainings.</li><li>
Maximize customer case support capability through proper planning and scheduling techniques.
</li><li>Stay current on company products instructions for use (IFU), best practices and technical troubleshooting, as well as relevant scientific clinical literature and new product information.</li></ul>
Sales :
<ul><li>Use consultative selling techniques to identify potential sales opportunities within the account.</li><li>
Creates awareness of BWI solutions and facilitates Clinical Development Manager contact with the key decision makers to drive incremental business.
</li><li>Drive collaboration and maintain consistent, open lines of communication across the assigned responsibilities with the local team.</li><li>
Develop and grow mutually beneficial customer relationships within and beyond the EP lab, including, but not limited to physicians, nurses and technicians, clinical and hospital administrators and staff.</li></ul>
Team :
<ul><li>Collaborate with peers to share best practices to increase value for customers.
</li><li>Ensure personal and Company compliance with government, company regulations, policies, and procedures.
</li><li>Prioritize and appropriately respond to requests in a high-stress environment.
</li><li>Maintain composure and problem-solving focus during stressful interactions.
</li><li>Engage in diagnostic dialogue with multiple internal and external business partners and stakeholders, and formulate solutions based on dialogue and input gained during session.
</li><li>Provide mentoring for new BWI commercial team members as requested.
</li><li>Respond daily to requests by email and phone call from customers, practitioners and partners.</li><li>
Perform administrative work, including managing account documentation, compliance training requirements, expense reporting, and Company system input.</li><li>
Maintain Safe Fleet standards according to Company guidelines.
</li><li>Communicate business related issues or opportunities to next management level.
</li><li>Ensure subordinates follow all Company guidelines related to Health, Safety and Environmental practices and that all resources needed to do so are available and in good condition.
</li><li>Additional duties as needed</li></ul></div></div></div></div></div></div></div></div></div><div>
Qualifications</div><div><div><div><div><div><div><div><div><div><ul><li>
Required Qualifications: A minimum of a Bachelor&rsquo;s degree</li><li>
Located in Trabzon or Rize</li><li>
A valid Driver&rsquo;s License</li><li>
The ability to travel related to this role is required. Must be willing and able to travel up to 40% overnight nationally.</li><li>
Position requires sitting for extended periods of time, working in a hospital laboratory setting, attending live patient cases, and wearing protective gear (i.e. lead aprons), and willing to work variable hours to meet patient needs</li><li>
Clinical Support Certificate</li><li>
May be required to lift up to 30 kg</li></ul>
Preferred Qualifications:<ul><li>
Electrophysiology/Cath Lab or EP/Cardiovascular Device Industry experience.
</li><li>Experience working with highly complex technical systems and/or working in a critical patient care setting.</li><li>
Effective and timely communicator with co-workers and all levels of patient care team.</li><li>
Self-starter who performs well with autonomy and can be flexible in a dynamic work environment.</li><li>
Problem solver who can think critically in high pressure environments.</li><li>
Receptive to constructive feedback and collaborates and works well in team environment.</li><li>
Able to take large amounts of data and translate information into actionable insights</li><li>
Hunger for learning and building new skills</li></ul></div></div></div></div></div></div></div></div></div>
Required Skills:
Preferred Skills:
<div>Qualifications</div><div><div><div><div><div><div><div><div><div><ul><li>
Required Qualifications: A minimum of a Bachelor&rsquo;s degree</li><li>
Located in Trabzon or Rize</li><li>
A valid Driver&rsquo;s License</li><li>
The ability to travel related to this role is required. Must be willing and able to travel up to 40% overnight nationally.</li><li>
Position requires sitting for extended periods of time, working in a hospital laboratory setting, attending live patient cases, and wearing protective gear (i.e. lead aprons), and willing to work variable hours to meet patient needs</li><li>
Clinical Support Certificate</li><li>
May be required to lift up to 30 kg</li></ul>
Preferred Qualifications:<ul><li>
Electrophysiology/Cath Lab or EP/Cardiovascular Device Industry experience.
</li><li>Experience working with highly complex technical systems and/or working in a critical patient care setting.</li><li>
Effective and timely communicator with co-workers and all levels of patient care team.</li><li>
Self-starter who performs well with autonomy and can be flexible in a dynamic work environment.</li><li>
Problem solver who can think critically in high pressure environments.</li><li>
Receptive to constructive feedback and collaborates and works well in team environment.</li><li>
Able to take large amounts of data and translate information into actionable insights</li><li>
Hunger for learning and building new skills</li></ul></div></div></div></div></div></div></div></div></div></div>

Klinik Geliştirme Asistanı - Clinical Development Assistant (TRABZON & RIZE)

<div>At Johnson &amp; Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
MedTech Sales
Job Sub Function:
Clinical Sales &ndash; Hospital/Hospital Systems (Commission)
Job Category:
Professional
All Job Posting Locations:
Diyarbak&#305;r, El&acirc;z&#305;&#287;, Malatya
Job Description:
Biosense Webster, Inc., a member of Johnson &amp; Johnson's Family of Companies, is recruiting for a Clinical Development Assistant to support Southeastern Territory (Malatya, Diyarbak&#305;r, Elaz&#305;g)
At Biosense Webster, Inc. we have one goal &mdash; to ensure those with cardiac arrhythmias can live the lives they want. This means transforming the latest advancements in electrophysiology into a suite of tools that empowers physicians with a range of treatments for the best outcomes.
Quality products and approaches are achievable only through collaboration with the smartest minds in electrophysiology. For more than 30 years, we&rsquo;ve been the global market leader in the science and technology of cardiac arrhythmia treatment, working with thousands of electrophysiologists to identify and develop diagnostic and treatment tools. And through onsite training, online courses and our global education centers, we work together to set new standards every day.
Learn more about Biosense Webster at www.biosensewebster.com and follow us on LinkedIn.
As the Clinical Development Specialist, you will:
Clinical :<ul><li>
Provide expert clinical product and technical assistance and training to physicians and EP Lab Staff on the effective use of BWI&rsquo;s systems and catheter equipment (e.g., The CARTO&reg; System and associated software modules and RF generator) during case procedures within an assigned geography, and in a manner that leads to meeting and exceeding business goals.
</li><li>Educate customers on all BWI products to optimize effective usage by providing technical and clinical information and in-service trainings.</li><li>
Maximize customer case support capability through proper planning and scheduling techniques.
</li><li>Stay current on company products instructions for use (IFU), best practices and technical troubleshooting, as well as relevant scientific clinical literature and new product information.</li></ul>
Sales :
<ul><li>Use consultative selling techniques to identify potential sales opportunities within the account.</li><li>
Creates awareness of BWI solutions and facilitates Clinical Development Manager contact with the key decision makers to drive incremental business.
</li><li>Drive collaboration and maintain consistent, open lines of communication across the assigned responsibilities with the local team.</li><li>
Develop and grow mutually beneficial customer relationships within and beyond the EP lab, including, but not limited to physicians, nurses and technicians, clinical and hospital administrators and staff.</li></ul>
Team :
<ul><li>Collaborate with peers to share best practices to increase value for customers.
</li><li>Ensure personal and Company compliance with government, company regulations, policies, and procedures.
</li><li>Prioritize and appropriately respond to requests in a high-stress environment.
</li><li>Maintain composure and problem-solving focus during stressful interactions.
</li><li>Engage in diagnostic dialogue with multiple internal and external business partners and stakeholders, and formulate solutions based on dialogue and input gained during session.
</li><li>Provide mentoring for new BWI commercial team members as requested.
</li><li>Respond daily to requests by email and phone call from customers, practitioners and partners.</li><li>
Perform administrative work, including managing account documentation, compliance training requirements, expense reporting, and Company system input.</li><li>
Maintain Safe Fleet standards according to Company guidelines.
</li><li>Communicate business related issues or opportunities to next management level.
</li><li>Ensure subordinates follow all Company guidelines related to Health, Safety and Environmental practices and that all resources needed to do so are available and in good condition.
</li><li>Additional duties as needed</li></ul>
Qualifications<ul><li>
Required Qualifications: A minimum of a Bachelor&rsquo;s degree</li><li>
Located in Diyarbakir, Malatya or Elazig</li><li>
A valid Driver&rsquo;s License</li><li>
The ability to travel related to this role is required. Must be willing and able to travel up to 40% overnight nationally.</li><li>
Position requires sitting for extended periods of time, working in a hospital laboratory setting, attending live patient cases, and wearing protective gear (i.e. lead aprons), and willing to work variable hours to meet patient needs</li><li>
Clinical Support Certificate</li><li>
May be required to lift up to 30 kg</li></ul>
Preferred Qualifications:<ul><li>
Electrophysiology/Cath Lab or EP/Cardiovascular Device Industry experience.
</li><li>Experience working with highly complex technical systems and/or working in a critical patient care setting.</li><li>
Effective and timely communicator with co-workers and all levels of patient care team.</li><li>
Self-starter who performs well with autonomy and can be flexible in a dynamic work environment.</li><li>
Problem solver who can think critically in high pressure environments.</li><li>
Receptive to constructive feedback and collaborates and works well in team environment.</li><li>
Able to take large amounts of data and translate information into actionable insights</li><li>
Hunger for learning and building new skills</li></ul>
Required Skills:
Preferred Skills:
Qualifications<ul><li>
Required Qualifications: A minimum of a Bachelor&rsquo;s degree</li><li>
Located in Diyarbakir, Malatya or Elazig</li><li>
A valid Driver&rsquo;s License</li><li>
The ability to travel related to this role is required. Must be willing and able to travel up to 40% overnight nationally.</li><li>
Position requires sitting for extended periods of time, working in a hospital laboratory setting, attending live patient cases, and wearing protective gear (i.e. lead aprons), and willing to work variable hours to meet patient needs</li><li>
Clinical Support Certificate</li><li>
May be required to lift up to 30 kg</li></ul>
Preferred Qualifications:<ul><li>
Electrophysiology/Cath Lab or EP/Cardiovascular Device Industry experience.
</li><li>Experience working with highly complex technical systems and/or working in a critical patient care setting.</li><li>
Effective and timely communicator with co-workers and all levels of patient care team.</li><li>
Self-starter who performs well with autonomy and can be flexible in a dynamic work environment.</li><li>
Problem solver who can think critically in high pressure environments.</li><li>
Receptive to constructive feedback and collaborates and works well in team environment.</li><li>
Able to take large amounts of data and translate information into actionable insights</li><li>
Hunger for learning and building new skills</li></ul></div>

Klinik Geliştirme Asistanı - Clinical Development Assistant (DIYARBAKIR , MALATYA , ELAZIG)

<div>At Johnson &amp; Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
MedTech Sales
Job Sub Function:
Clinical Sales &ndash; Hospital/Hospital Systems (Commission)
Job Category:
Professional
All Job Posting Locations:
Istanbul, Turkey
Job Description:
Biosense Webster, Inc., a member of Johnson &amp; Johnson's Family of Companies, is recruiting for a Clinical Development Assistant to support &#304;stanbul territory
At Biosense Webster, Inc. we have one goal &mdash; to ensure those with cardiac arrhythmias can live the lives they want. This means transforming the latest advancements in electrophysiology into a suite of tools that empowers physicians with a range of treatments for the best outcomes.
Quality products and approaches are achievable only through collaboration with the smartest minds in electrophysiology. For more than 30 years, we&rsquo;ve been the global market leader in the science and technology of cardiac arrhythmia treatment, working with thousands of electrophysiologists to identify and develop diagnostic and treatment tools. And through onsite training, online courses and our global education centers, we work together to set new standards every day.
Learn more about Biosense Webster at www.biosensewebster.com and follow us on LinkedIn.
As the Clinical Development Specialist, you will:
Clinical :<ul><li>
Provide expert clinical product and technical assistance and training to physicians and EP Lab Staff on the effective use of BWI&rsquo;s systems and catheter equipment (e.g., The CARTO&reg; System and associated software modules and RF generator) during case procedures within an assigned geography, and in a manner that leads to meeting and exceeding business goals.
</li><li>Educate customers on all BWI products to optimize effective usage by providing technical and clinical information and in-service trainings.</li><li>
Maximize customer case support capability through proper planning and scheduling techniques.
</li><li>Stay current on company products instructions for use (IFU), best practices and technical troubleshooting, as well as relevant scientific clinical literature and new product information.</li></ul>
Sales :
<ul><li>Use consultative selling techniques to identify potential sales opportunities within the account.</li><li>
Creates awareness of BWI solutions and facilitates Clinical Development Manager contact with the key decision makers to drive incremental business.
</li><li>Drive collaboration and maintain consistent, open lines of communication across the assigned responsibilities with the local team.</li><li>
Develop and grow mutually beneficial customer relationships within and beyond the EP lab, including, but not limited to physicians, nurses and technicians, clinical and hospital administrators and staff.</li></ul>
Team :
<ul><li>Collaborate with peers to share best practices to increase value for customers.
</li><li>Ensure personal and Company compliance with government, company regulations, policies, and procedures.
</li><li>Prioritize and appropriately respond to requests in a high-stress environment.
</li><li>Maintain composure and problem-solving focus during stressful interactions.
</li><li>Engage in diagnostic dialogue with multiple internal and external business partners and stakeholders, and formulate solutions based on dialogue and input gained during session.
</li><li>Provide mentoring for new BWI commercial team members as requested.
</li><li>Respond daily to requests by email and phone call from customers, practitioners and partners.</li><li>
Perform administrative work, including managing account documentation, compliance training requirements, expense reporting, and Company system input.</li><li>
Maintain Safe Fleet standards according to Company guidelines.
</li><li>Communicate business related issues or opportunities to next management level.
</li><li>Ensure subordinates follow all Company guidelines related to Health, Safety and Environmental practices and that all resources needed to do so are available and in good condition.
</li><li>Additional duties as needed</li></ul>
Qualifications<ul><li>
Required Qualifications: A minimum of a Bachelor&rsquo;s degree</li><li>
Located in Istanbul</li><li>
A valid Driver&rsquo;s License</li><li>
The ability to travel related to this role is required. Must be willing and able to travel up to 40% overnight nationally.</li><li>
Position requires sitting for extended periods of time, working in a hospital laboratory setting, attending live patient cases, and wearing protective gear (i.e. lead aprons), and willing to work variable hours to meet patient needs</li><li>
Clinical Support Certificate</li><li>
May be required to lift up to 30 kg</li></ul>
Preferred Qualifications:<ul><li>
Electrophysiology/Cath Lab or EP/Cardiovascular Device Industry experience.
</li><li>Experience working with highly complex technical systems and/or working in a critical patient care setting.</li><li>
Effective and timely communicator with co-workers and all levels of patient care team.</li><li>
Self-starter who performs well with autonomy and can be flexible in a dynamic work environment.</li><li>
Problem solver who can think critically in high pressure environments.</li><li>
Receptive to constructive feedback and collaborates and works well in team environment.</li><li>
Able to take large amounts of data and translate information into actionable insights</li><li>
Hunger for learning and building new skills</li></ul>
Required Skills:
Preferred Skills:
Qualifications<ul><li>
Required Qualifications: A minimum of a Bachelor&rsquo;s degree</li><li>
Located in Istanbul</li><li>
A valid Driver&rsquo;s License</li><li>
The ability to travel related to this role is required. Must be willing and able to travel up to 40% overnight nationally.</li><li>
Position requires sitting for extended periods of time, working in a hospital laboratory setting, attending live patient cases, and wearing protective gear (i.e. lead aprons), and willing to work variable hours to meet patient needs</li><li>
Clinical Support Certificate</li><li>
May be required to lift up to 30 kg</li></ul>
Preferred Qualifications:<ul><li>
Electrophysiology/Cath Lab or EP/Cardiovascular Device Industry experience.
</li><li>Experience working with highly complex technical systems and/or working in a critical patient care setting.</li><li>
Effective and timely communicator with co-workers and all levels of patient care team.</li><li>
Self-starter who performs well with autonomy and can be flexible in a dynamic work environment.</li><li>
Problem solver who can think critically in high pressure environments.</li><li>
Receptive to constructive feedback and collaborates and works well in team environment.</li><li>
Able to take large amounts of data and translate information into actionable insights</li><li>
Hunger for learning and building new skills</li></ul></div>

Amgen

<div>Join Amgen&rsquo;s Mission of Serving Patients
At Amgen, if you feel like you&rsquo;re part of something bigger, it&rsquo;s because you are. Our shared mission&mdash;to serve patients living with serious illnesses&mdash;drives all that we do.
Since 1980, we&rsquo;ve helped pioneer the world of biotech in our fight against the world&rsquo;s toughest diseases. With our focus on four therapeutic areas &ndash;Oncology, Inflammation, General Medicine, and Rare Disease&ndash; we reach millions of patients each year. As a member of the Amgen team, you&rsquo;ll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives.
Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lay within them, you&rsquo;ll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career.
Live
What you will do
Let&rsquo;s do this! Let&rsquo;s change the world! The role provides proactive end to end quality support for the development and implementation of a risk-based quality assurance strategy for the clinical development program.
The role will support end to end quality oversight of the General Medicine &amp; Obesity Therapeutic Area and will be responsible for supporting a risk-based quality strategy that advances quality by design principles for the full clinical trial lifecycle (protocol development, database lock, and regulatory submissions/ approvals).
You will play a vital role by developing deep knowledge of the clinical trials you support and provide oversight and quality management of critical data and processes for global and local study teams and all clinical trial sites who participate in Amgen sponsored trials.
Responsibilities<ul><li>
Act as a Good Clinical Practice (GCP) Subject Matter Expert, offering independent, objective quality guidance.</li><li>
Oversee quality across all clinical development stages.</li><li>
Plan and execute risk-based GCP audits (sites, affiliates, vendors, studies).</li><li>
Support regulatory inspections and guide responses, including root cause analysis and CAPAs.</li><li>
Lead quality oversight of Risk Assessment Categorization Tools (RACT) for each trial.</li><li>
Facilitate monthly quality risk reviews with clinical program leaders.</li><li>
Manage audit findings, deviations, and CAPA responses.</li><li>
Ensure regional compliance with local regulations and support vendor evaluations.</li><li>
Analyze data quality trends, identify gaps, and implement corrective actions.</li><li>
Oversee technologies for endpoint data collection (e.g., biomarkers, imaging).</li><li>
Develop and execute TA-specific QA plans and protocol-specific audit strategies.</li><li>
Support quality management activities including deviations, breaches, and inspection readiness.</li><li>
Drive innovation in quality oversight using data analytics, AI, and NLP.</li><li>
Review protocols to simplify design and identify critical data/processes.</li></ul>
Country/ Regional Quality Leadership<ul><li>
Manage analytical tools and data trends to address site/regional quality gaps.</li><li>
Provide oversight for key sites in collaboration with regional operations.</li><li>
Conduct Quality Partnership Visit at key sites within the country/Region</li><li>
Share best practices and compliance insights with stakeholders.</li><li>
Offer independent quality consultation and escalate issues as needed.</li><li>
Support local vendor assessments and pre-inspection activities.</li><li>
Conduct regional risk assessments for audit planning.</li><li>
Stay current on regulatory trends and deliver ongoing training.</li></ul>
Win
WHAT WE EXPECT OF YOU
We are all different, yet we all use our unique contributions to serve patients. The individual we seek has technological literacy and leadership skills, and has these qualifications:
Doctorate degree and 2 years of Quality Management, Quality Assurance and Good Clinical Practices experience in the pharmaceutical/biotech industry where risk-based quality management and quality by design are a core responsibility.
Or
Master&rsquo;s degree and 4 years of the previous mentioned experience
Or
Bachelor&rsquo;s degree and 6 years of the previous mentioned experience
Or
Associate&rsquo;s degree and 10 years of the previous mentioned experience<ul><li>
Oversight and implementation of Quality Management Systems and experience managing quality in electronic QMS such as Veeva or Track wise.</li><li>
Thorough understanding of Clinical R&amp;D activities and Global Regulations.</li><li>
Experience with Regulatory Submission and Inspection Management procedures.</li><li>
Quality Oversight of Clinical Trials, including clinical trial protocol development, execution, and submissions.</li><li>
Leadership or mentoring experience is ideal, in a regional capacity would be phenomenal.</li><li>
Excellent verbal and written communication skills, including strong business writing abilities and active listening. Able to understand and articulate technical concepts and literature in spoken and written English.</li><li>
Ability to transform business and stakeholder feedback into clear, efficient processes using a straightforward language and format.</li><li>
Self-driven with strong analytical, critical-thinking, prioritization, and decision-making abilities.</li></ul><h2 class="jobSectionHeader">
IMPORTANT! Please submit your resume/CV in English!</h2><h2 class="jobSectionHeader">
Thrive</h2>
WHAT YOU CAN EXPECT OF US<ul><li>
Vast opportunities to learn, develop, and move up and across our global organization.</li><li>
Diverse and inclusive community of belonging, where colleagues are empowered to bring ideas to the table, take risks, and act.</li><li>
Generous Amgen Total Rewards Plan comprising healthcare, finance, wealth and career benefits.</li><li>
Flexible work arrangements.</li></ul><h2 class="jobSectionHeader">
Apply now</h2>
In our quest to serve patients above all else, Amgen is the first to imagine, and the last to doubt. Join us: Careers.amgen.com
As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other and live the Amgen values to continue advancing science to serve patients. Together, we compete in the fight against serious disease.
Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or any other basis protected by applicable law.
We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.</div>

Quality Compliance Senior Manager

Gilead Sciences

<div>
 At Gilead, we&rsquo;re creating a healthier world for all people. For more than 35 years, we&rsquo;ve tackled diseases such as HIV, viral hepatitis, COVID-19 and cancer &ndash; working relentlessly to develop therapies that help improve lives and to ensure access to these therapies across the globe. We continue to fight against the world&rsquo;s biggest health challenges, and our mission requires collaboration, determination and a relentless drive to make a difference.
 
 
 Every member of Gilead&rsquo;s team plays a critical role in the discovery and development of life-changing scientific innovations. Our employees are our greatest asset as we work to achieve our bold ambitions, and we&rsquo;re looking for the next wave of passionate and ambitious people ready to make a direct impact.
 
 
 We believe every employee deserves a great leader. People Leaders are the cornerstone to the employee experience at Gilead and Kite. As a people leader now or in the future, you are the key driver in evolving our culture and creating an environment where every employee feels included, developed and empowered to fulfil their aspirations. Join Gilead and help create possible, together.
 
 
 
 Job Description
 
 
 
 Regulatory Affairs Manager Turkiye; is responsible from managing RA submissions &amp; supporting Clinical Trials applications and will serve as a core member of the affiliate Regulatory Team interacting with local Regulatory Authorities and other stakeholders to ensure that the company complies with country&rsquo;s applicable legislations.
 
 
 
 Knowledge &amp; Details
 
 
 
 <ul>
 <li>
 Manage regulatory submissions to local HA submissions inc. but not limited to Pre-MAA related activities (GMP &amp; prioritization applications), marketing Authorisation (MA) applications &amp; variations and other MA maintenance applications, in line with local HA expectations, Gilead SOPs and business objectives for assigned product(s) or projects.
 </li>
 <li>
 Stay up to date with local and global regulatory requirements (including ICH), internal policies and support the organization in adapting to legislative changes.
 </li>
 <li>
 Responsible from ensuring the updates to commercial product packaging and labelling in line with product licenses.
 </li>
 <li>
 Manage clinical trial applications, amendments, and notifications. Collaborate with Clinical Operations and the CT Hub to complete CT submissions to MOH timely and interacts with cross-functional teams internally and externally to ensure submission package fulfils the MoH requirements on time.
 </li>
 <li>
 Ensure ongoing clinical trials comply with local legislation and oversee investigational product packaging and labelling approvals.
 </li>
 <li>
 Plan regulatory and clinical timelines and strategies under the guidance of the Regulatory Affairs Director.
 </li>
 <li>
 Ensure good and strong relationships with functional areas of the local organization (Medical Affairs, Commercial, Market Access, Legal, etc.) and with Gilead Sciences Global/Regional RA in order to ensure the success of local and international business results from the regulatory point of view.
 </li>
 <li>
 Build and maintain networks with regulatory stakeholders, including decision-makers and influencers.
 </li>
 <li>
 Develop and implement regulatory and clinical trial strategies, and manage negotiations with health authorities.
 </li>
 <li>
 Actively contribute to local and global initiatives that improve regulatory processes.
 
 
 </li>
 </ul>
 
 Professional Experience / Key Skills
 
 
 
 <ul>
 <li>
 Solid experience in total in Regulatory Affairs &amp; Clinical Trials (if possible) related experience in the Pharmaceutical / Biotech Industry. An advanced degree is desirable.
 </li>
 <li>
 Degree in Pharmaceutical Sciences or equivalent discipline is preferred.
 </li>
 <li>
 Proven ability to prioritize, conduct, and manage time to meet project deadlines.
 </li>
 <li>
 Good influencing and negotiating skills. Must be capable of developing and implementing regulatory initiatives and managing negotiations with Regulatory Authorities.
 </li>
 <li>
 Demonstrates leadership skills with a sphere of influence externally, cross-functionally and within the RA and the affiliate.
 </li>
 <li>
 Strong focus on achievement of goals and continuous improvement
 </li>
 <li>
 Solution-oriented and innovative; can identify creative options for resolving issues that respond to multiple stakeholder interests and needs.
 </li>
 <li>
 Having excellence in multiple project management, good communication and interpersonal skills.
 </li>
 <li>
 Be an analytical thinker, problem solver, proactive, initiative taker, creative personality
 </li>
 <li>
 Team player who actively contributes to the team in order to complete tasks, meet goals or manage projects, actively listen others, respect ideas and aim to improve the process.
 </li>
 <li>
 Fluency in spoken and written English.
 </li>
 <li>
 Good decision-making skills are important.
 </li>
 <li>
 Excellent verbal, written, organization skills and interpersonal communication skills required.
 
 
 </li>
 </ul>
 Equal Employment Opportunity (EEO)
 
 
 It is the policy of Gilead Sciences, Inc. and its subsidiaries and affiliates (collectively "Gilead" or the "Company") to recruit select and employ the most qualified persons available for positions throughout the Company. Except if otherwise provided by applicable law, all employment actions relating to issues such as compensation, benefits, transfers, layoffs, returns from layoffs, company-sponsored training, education assistance, social and recreational programs are administered on a non-discriminatory basis (i.e. without regard to protected characteristics or prohibited grounds, which may include an individual&rsquo;s gender, race, color, national origin, ancestry, religion, creed, physical or mental disability, marital status, sexual orientation, medical condition, veteran status, and age, unless such protection is prohibited by federal, state, municipal, provincial, local or other applicable laws). Gilead also prohibits discrimination based on any other characteristics protected by applicable laws.
 
 
 
 For Current Gilead Employees And Contractors
 
 
 
 Please apply via the Internal Career Opportunities portal in Workday.
</div>

Regulatory Affairs Manager

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Quality Compliance Senior Manager

Regulatory Affairs Manager