manager of medical

Exeltis Turkey

<div>
 
 
 Medical Manager
 
 
 
 
 
 
 We are looking for a Medical Manager to be assigned to our Head Office at Exeltis Turkey.
 
 
 
 
 
 
 Qualifications
 
 
 <ul>
 <li>
 Medical Doctor (MD) degree,
 </li>
 <li>
 Excellent command of written and spoken English,
 </li>
 <li>
 Proficient in MS Office applications and effective presentation techniques,
 </li>
 <li>
 Strong sense of responsibility with analytical and strategic thinking skills,
 </li>
 <li>
 Holder of a valid B-class driving license and actively driving,
 </li>
 <li>
 No restrictions on travel.
 </li>
 <li>
 Experience in Respiratory Field will be preferred
 </li>
 </ul>
 
 
 
 
 
 Job Description
 
 
 <ul>
 <li>
 Providing continuous medical update and support for existing products,
 </li>
 <li>
 Represent the company at Scientific Congresses, trainings, and medical meetings,
 </li>
 <li>
 Provide medical support to Marketing and Sales teams during scientific presentations,
 </li>
 <li>
 Contribute medical insights to product strategies,
 </li>
 <li>
 Conduct meetings with key opinion leaders (KOLs) and Health Authorities regarding assigned products,
 </li>
 <li>
 Plan, initiate, and monitor clinical research activities,
 </li>
 <li>
 Oversee pharmacovigilance operations and ensure the pharmacovigilance system remains compliant with current regulatory requirements
 </li>
 </ul>
 
 
</div>

Medical Manager

MediPharma Konnect

Hiring *Manager &ndash; Medical Affairs / Advisor* with leading organization at *Ahmedabad.**CTC* - Up to 30.00 LPA*Candidate profile-* MBBS / MD / PhD in life sciences or related field with 2&ndash;5+ years of experience in Medical Affairs, Clinical Research, or Medical Information.*Role &amp; Responsibilities*-Provide scientific and clinical expertise to launch and lifecycle management of a new product as medical-scientific expert, ensuring compliant communication and medical information.  Serve as the subject matter expert for the new product develop and execute new medico marketing plans for doctor awareness with training of team. Build strong relationships with KOLs, HCPs, and scientific societies.  Identify research opportunities and support company-sponsored and investigator-initiated studies.  Ensure compliance with local regulatory, ethical, and pharmacovigilance requirements.  Partner with marketing, regulatory, market access, sales, and commercial teams for aligned strategies.*Mail id* &ndash; medipharma.hrm3@gmail.com / 9391176708*Medi Pharma Konnect* (One stop solution for Pharma &amp; Healthcare)Job Type: Full-timePay: Up to ₹3,000,000.00 per yearWork Location: In person

Manager - Medical Affairs/Medical Advisor

Abdi Ibrahim Pharmaceuticals

<div>
 
 Abdi &Idot;brahim, founded in 1912, has the largest product portfolio in the sector and is the largest employer in the Turkish pharmaceutical industry with 5.500 employees. Abdi &Idot;brahim has been the leader of Turkey&rsquo;s pharmaceutical industry since 2002 with its powerful vision. Today, Abdi &Idot;brahim operates in 17 countries outside Turkey, exports to more than 70 countries ranging from Canada to European Union member states, from North Africa to Asia. As a corporate citizen working towards creating a better world and a better future, adhering to its mission in the sector and to the requirements of societal priorities, Abdi &Idot;brahim focuses on sustainability in all its business processes. Its vision for 2025 - apart from maintaining its status as a wholly local company - is to become "one of the top 100 pharmaceutical companies in the world.
 
 We&rsquo;re currently looking for a Senior / Medical Manager.
 
 
 
 
 
 
 
 The key duties of the successful candidate are:
 
 
 
 
 
 <ul>
 <li>
 Have a university degree in medicine (MD),
 </li>
 <li>
 Preferably speciality in a therapeutical area
 </li>
 <li>
 Preferably at least 1 year of experience as Medical Manager in pharmaceutical industry,
 </li>
 <li>
 Good command of written and spoken English
 </li>
 <li>
 Proficiency in MS Office applications
 </li>
 <li>
 Deliver strong teamwork within matrix organization
 </li>
 <li>
 Excellent communication and presentation skills
 </li>
 <li>
 Planning and organization &amp; time management skills
 </li>
 <li>
 Analytical thinking, result oriented, quality focused and efficient way of work, open to growth
 </li>
 <li>
 No restriction to travel frequently and must have a valid driving license
 </li>
 </ul>
 
 
 
 
 
 The key duties of the successful candidate are:
 
 
 
 
 
 <ul>
 <li>
 Providing medical guidance to regulatory, marketing and clinical research teams,
 </li>
 <li>
 Providing medical training activities for sales force; preparing and reviewing all visual materials and training manuals,
 </li>
 <li>
 Searching for new data, literature to provide updated medical data for medico-marketing activities,
 </li>
 <li>
 Participating scientific congresses, symposia, trainings and representing the company,
 </li>
 <li>
 Creating and implementing medico-marketing projects,
 </li>
 </ul>
 
 
 
 
 Applicants with suitable qualifications are kindly invited to apply through LinkedIn. All applications will be acknowledged and treated confidentially.
 
</div>

DEVA Holding A.Ş.

<div>
 
 
 QUALIFICATIONS
 
 
 
 
 
 
 DEVA has been operating since 1958 and is one of the pioneering pharmaceutical companies in Turkey. DEVA, having R&amp;D in focus, manufactures with international quality standards and currently exports products to other countries worldwide.
 
 
 
 
 
 DEVA is seeking for a
 
 Medical Manager
 
 ;
 
 
 
 
 
 &bull; University degree in Medicine, Dentistry, Pharmacy, Veterinary,
 
 
 &bull; Must have been completed obligatory service as Doctor for new Medicine graduaters,
 
 
 &bull; Preferably 1 year experience in Medical Department,
 
 
 &bull; Excellent command of both written and spoken
 
 English &amp; German
 
 ,
 
 
 &bull; Computer literacy, good knowledge of MS Office tools,
 
 
 &bull; Excellent interpersonal, communication and presentation skills,
 
 
 &bull; Result oriented in a competitive business environment,
 
 
 &bull; Valid driver&rsquo;s licence,
 
 
 &bull; No restrictions for travel domestically and internationally,
 
 
 
 
 
 
 
 
 
 JOB DESCRIPTION
 
 
 
 
 
 
 &bull; Providing medical support to the development and marketing of products,
 
 
 &bull; Providing internal medical training activities for sales force; preparing and reviewing all training manuals and visual materials,
 
 
 &bull; Actively search for new data, literature, guidelines to provide updated medical background for medico-marketing activities,
 
 
 
 
 
 
 Bir &ccedil;al&inodot;&scedil;an aday&inodot; olarak, sizinle aram&inodot;zdaki t&uuml;m ileti&scedil;imde bilgilerinizi 6698 say&inodot;l&inodot; Ki&scedil;isel Verilerin Korunmas&inodot; Kanunu&rsquo;na, yasal mevzuata ve Ki&scedil;isel Verileri Koruma Kurumu kararlar&inodot;na uygun olarak i&scedil;liyoruz. Detayl&inodot; bilgiye ve ayd&inodot;nlatma metnimize link &uuml;zerinden ula&scedil;abilirsiniz. https://www.deva.com.tr/tr/kvkk
 
 
</div>

Unilever

<div>
 
 Job Title:
 
 Manager (Medical Doctor), Global Market Vigilance (GMV)
 
 
 
 Location:
 
 Unilever Bangalore R&amp;D
 
 
 
 Function:
 
 Global Regulatory Affairs (GRA), Wellbeing Collective (WBC)
 
 
 
 Job Summary
 
 
 
 The ideal candidate is a medical doctor who can leverage their healthcare professional background and hands-on experience in Pharmacovigilance to ensure the highest standards of safety assessment and regulatory compliance. The role applying clinical judgment, conducting in depth adverse event reviews, and contributing proactively to ensure the safety of our products and consumers.
 
 
 
 Key Responsibilities
 
 
 
 <ul>
 <li>
 Case Assessment and Medical/ Clinical Review:
 </li>
 <ul>
 <li>
 Conduct comprehensive and in-depth review of health-related complaints (i.e. adverse events or AEs) regarding our products received from various sources (consumers, healthcare professionals, clinical studies, etc.)
 </li>
 <li>
 Evaluate case seriousness, expectedness, and identify any missing or incomplete information while ensuring data integrity and accuracy.
 </li>
 <li>
 Ensure all AEs are documented and coded accurately using industry-standard medical terminologies like MedDRA (Medical Dictionary for Regulatory Activities).
 </li>
 <li>
 Actively participate in the analysis of aggregate safety data to identify potential safety signals or trends.
 </li>
 </ul>
 <li>
 Global Regulatory Compliance and Quality Assurance:
 </li>
 <ul>
 <li>
 Ensure all medical review and case processing activities are executed in strict adherence to a complex web of global and local regulatory requirements (e.g., FDA 21 CFR 312, EMA Good Pharmacovigilance Practices (GVP), etc.) and internal Standard Operating Procedures (SOPs).
 </li>
 <li>
 Contribute to internal and external audits and inspections, acting as a subject matter expert on adverse event case management.
 </li>
 </ul>
 <li>
 Strategic Cross-Functional Collaboration:
 </li>
 <ul>
 <li>
 Serve as a key liaison for safety-related inquiries from internal partners, including Legal, Marketing, R&amp;D, and Quality Assurance.
 </li>
 </ul>
 <li>
 Mentorship and Continuous Improvement:
 </li>
 <ul>
 <li>
 Serve as a mentor to team members working in AE management process and provide training as well as guidance on case assessment approaches.
 </li>
 <li>
 Identify and propose improvements to existing workflows and tools to enhance efficiency, accuracy, and compliance within the GMV team.
 
 </li>
 </ul>
 </ul>
 
 Required Skills, Qualifications, And Experience
 
 
 
 <ul>
 <li>
 Education: Medical degree (MBBS or MD) from an accredited institution is required.
 </li>
 <li>
 Experience:
 </li>
 <ul>
 <li>
 Minimum of 3+ years of strong expertise in pharmacovigilance and patient/ consumer safety working in the Pharmaceutical, Medical Device or Consumer Healthcare industries.
 </li>
 <li>
 Extensive firsthand experience using global pharmacovigilance databases. Experience with Veeva Vault Safety is highly desired.
 </li>
 <li>
 Ability to perform robust medical reviews and assessments of adverse event and serious adverse cases.
 </li>
 <li>
 Well versed in safety &amp; causality assessments, medical narrative writing, using MedDRA coding and reviewing MedWatch and CIOMS reports.
 </li>
 </ul>
 <li>
 Technical and Professional Skills:
 </li>
 <ul>
 <li>
 Medical and Scientific Knowledge: Strong foundational understanding of human physiology, clinical pharmacology as well as side effects associated with use of pharmaceuticals, medical devices, consumer products etc. Ability to apply this knowledge to interpret consumer complaint information, clinical data, lab results, and medical reports.
 </li>
 <li>
 Regulatory Acumen: In-depth knowledge of global pharmacovigilance regulations, guidelines, and industry best practices (especially US FDA, Health Canada).
 </li>
 <li>
 Communication &amp; Collaboration: Exceptional ability to communicate complex medical concepts clearly and concisely, both verbally and in writing, to both scientific and non-scientific audiences.
 </li>
 <li>
 Analytical Rigor: Excellent critical thinking and critical thinking skills with a meticulous diligence and a high degree of accuracy.
 
 </li>
 </ul>
 </ul>
 
 Our commitment to Equality, Diversity &amp; Inclusion
 
 
 
 Unilever embraces diversity and encourages applicants from all walks of life! This means giving full and fair consideration to all applicants and continuing development of all employees regardless of age, disability, gender reassignment, race, religion or belief, sex, sexual orientation, marriage and civil partnership, and pregnancy and maternity.
 
 
 
 "All official offers from Unilever are issued only via our Applicant Tracking System (ATS). Offers from individuals or unofficial sources may be fraudulent&mdash;please verify before proceeding."
 
</div>

Manager (Medical Doctor), Global Market Vigilance (GMV)

Hillcrest HealthCare System

<div>Overview:

Join our team as a Regional Manager of Medical Staff Services in Tulsa, OK.<div> 
Why Join Us?</div><div> 
Thrive in a People-First Environment and Make Healthcare Better</div><div><ul><li>
Thrive: We empower our team with career growth opportunities, tuition assistance, and resources that support your wellness, education, and financial well-being.</li><li>
People-First: We prioritize your well-being with paid time off, comprehensive health benefits, and a supportive, inclusive culture where you are valued and cared for.</li><li>
Make Healthcare Better: We use advanced technology to support our team and enhance patient care.</li></ul></div><div>
 Get to Know Your Team:</div><div><ul><li>
Hillcrest Medical Center is a 656-bed hospital that includes The Alexander Burn Center, The Peggy V. Helmerich Women&rsquo;s Health Center, Kaiser Rehabilitation Center, the latest technology for the treatment of cancer, and the Oklahoma Heart Institute.
</li></ul></div>Responsibilities:

The Regional Manager of the Medical Staff Services will oversee the day-to-day operations of multiple facilities within assigned region and staff who assist with the credentialing activities for physicians and other independent practitioners at Hillcrest Health Systems (HHS). Will serve as a liaison between facility and market leadership, medical staff elected leaders and credentialing medical office staff. Subject matter expert in market and regional specifics related to medical staff governance including clinical services offered, medical staff bylaws, rules &amp; regulations, and related policies. Ensure regulatory survey preparedness, actively participating in regulatory related activities. Responsible for the coordination of all operational aspects of the assigned region, including organizing and conducting programs and establishing procedures for all medical staff functions. Assign workflow and oversee the tracking of medical professionals to ensure proper training, certifications, and experience, and licensures meet medical staff bylaws. Assign workflow and manage the review process of all physician files for completeness and &ldquo;red flags&rdquo; and acts to support the medical staff providers and staff in the credentialing process. Works closely with all HHS facilities and the provider groups to assist and oversee the facilitating the credentialing of the physicians and other healthcare providers. Works cooperatively with outside review organizations, hospital personnel, nursing services, ancillary services, and physicians in a friendly, courteous, and efficient manner to educate all parties regarding credentialing and the Medical Staff organization requirements as outlined in the Medical Staff Bylaws. Resolves complex questions regarding credentialing or provider database maintenance and best practices. Monitoring and tracking trends at each facility assigned. Manages and contributes to the development and processes and procedures. Overseeing recruitment, implementing regulations, monitoring budget, and staying updated on medical trends to ensure efficient operations and high- quality patient care. Assists in department staffing issues, such as annual evaluations, disciplinary actions, etc.
Qualifications:

Job Requirements:<ul><li>
High School Diploma or equivalent</li><li>
Associate's degree</li><li>
3 years of experience in medical staff services and credentialing</li><li>
3 years in a medical staff management role</li><li>
CPCS or CPMSM completed or in progress to complete</li></ul>
Preferred Job Requirements:<ul><li>
Bachelor's Degree.</li></ul></div>

Regional Medical Staff Manager

<div>Job Title: Manager (Medical Doctor), Global Market Vigilance (GMV)
Location: Unilever Bangalore R&amp;D
Function: Global Regulatory Affairs (GRA), Wellbeing Collective (WBC)
Job Summary
The ideal candidate is a medical doctor who can leverage their healthcare professional background and hands-on experience in Pharmacovigilance to ensure the highest standards of safety assessment and regulatory compliance. The role applying clinical judgment, conducting in depth adverse event reviews, and contributing proactively to ensure the safety of our products and consumers.
Key Responsibilities:<ul><li>
Case Assessment and Medical/ Clinical Review:<ul><li>
Conduct comprehensive and in-depth review of health-related complaints (i.e. adverse events or AEs) regarding our products received from various sources (consumers, healthcare professionals, clinical studies, etc.)</li><li>
Evaluate case seriousness, expectedness, and identify any missing or incomplete information while ensuring data integrity and accuracy.</li><li>
Ensure all AEs are documented and coded accurately using industry-standard medical terminologies like MedDRA (Medical Dictionary for Regulatory Activities).</li><li>
Actively participate in the analysis of aggregate safety data to identify potential safety signals or trends.</li></ul></li><li>
Global Regulatory Compliance and Quality Assurance:<ul><li>
Ensure all medical review and case processing activities are executed in strict adherence to a complex web of global and local regulatory requirements (e.g., FDA 21 CFR 312, EMA Good Pharmacovigilance Practices (GVP), etc.) and internal Standard Operating Procedures (SOPs).</li><li>
Contribute to internal and external audits and inspections, acting as a subject matter expert on adverse event case management.</li></ul></li><li>
Strategic Cross-Functional Collaboration:<ul><li>
Serve as a key liaison for safety-related inquiries from internal partners, including Legal, Marketing, R&amp;D, and Quality Assurance.</li></ul></li><li>
Mentorship and Continuous Improvement:<ul><li>
Serve as a mentor to team members working in AE management process and provide training as well as guidance on case assessment approaches.</li><li>
Identify and propose improvements to existing workflows and tools to enhance efficiency, accuracy, and compliance within the GMV team.</li></ul></li></ul>
Required Skills, Qualifications, and Experience<ul><li>
Education: Medical degree (MBBS or MD) from an accredited institution is required.</li><li>
Experience:<ul><li>
Minimum of 3+ years of strong expertise in pharmacovigilance and patient/ consumer safety working in the Pharmaceutical, Medical Device or Consumer Healthcare industries.</li><li>
Extensive firsthand experience using global pharmacovigilance databases. Experience with Veeva Vault Safety is highly desired.</li><li>
Ability to perform robust medical reviews and assessments of adverse event and serious adverse cases.</li><li>
Well versed in safety &amp; causality assessments, medical narrative writing, using MedDRA coding and reviewing MedWatch and CIOMS reports.</li></ul></li><li>
Technical and Professional Skills:<ul><li>
Medical and Scientific Knowledge: Strong foundational understanding of human physiology, clinical pharmacology as well as side effects associated with use of pharmaceuticals, medical devices, consumer products etc. Ability to apply this knowledge to interpret consumer complaint information, clinical data, lab results, and medical reports.</li><li>
Regulatory Acumen: In-depth knowledge of global pharmacovigilance regulations, guidelines, and industry best practices (especially US FDA, Health Canada).</li><li>
Communication &amp; Collaboration: Exceptional ability to communicate complex medical concepts clearly and concisely, both verbally and in writing, to both scientific and non-scientific audiences.</li><li>
Analytical Rigor: Excellent critical thinking and critical thinking skills with a meticulous diligence and a high degree of accuracy.</li></ul></li></ul>
Our commitment to Equality, Diversity &amp; Inclusion
Unilever embraces diversity and encourages applicants from all walks of life! This means giving full and fair consideration to all applicants and continuing development of all employees regardless of age, disability, gender reassignment, race, religion or belief, sex, sexual orientation, marriage and civil partnership, and pregnancy and maternity. 
 
&quot;All official offers from Unilever are issued only via our Applicant Tracking System (ATS). Offers from individuals or unofficial sources may be fraudulent&mdash;please verify before proceeding.&quot;</div>

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