scientific specialist

Mirus Consulting Group

<div>m&icirc;rus Consulting Group is a Puerto Rico based technical services firm headquartered in Humacao. The company specializes in Computer System Validation (CSV) and Information Technology consulting for the pharmaceutical and life sciences industries across Puerto Rico and parts of the United States. Its services include the assessment and validation of automation systems, network infrastructures, and business processes, as well as comprehensive project management support to ensure compliance, efficiency, and operational excellence.<br>
<br>
<b>Job Summary</b><br>
The Specialist Quality Control functions as the technical specialist for testing and development in areas of molecular biology and microbiology. Focus is on the complex technical issues and scope is typically multi-organizational and/or multi-site and /or involving outside resources. The Specialist Quality Control is responsible for supporting quality control laboratory operations within a regulated pharmaceutical environment. This role ensures compliance with quality standards, regulatory requirements, and internal procedures through scientific data analysis, method validation and transfer, sample management, and quality process management.<br>
<br>
<b>Key Responsibilities</b>
<ul><li>Perform and support <b>scientific data analysis</b> for Quality Control activities.</li>
<li>Strong <b>Technical Writing</b> (English and Spanish) mainly focuses.</li>
<li>Utilize Microsoft <b>Excel</b> as a primary tool for data analysis and trending.</li>
<li>Support <b>sample management</b> activities including receipt, tracking, testing, and disposition.</li>
<li>Participate in <b>project management</b> activities related to method validation, method transfer, and quality improvements.</li>
<li>Support and maintain <b>quality process management</b>, ensuring compliance with GMP and internal procedures.</li>
<li>Assist with <b>computer system validation</b> and analytical method validation (preferable experience).</li>
<li>Support equipment <b>preventive maintenance, basic troubleshooting</b>, and documentation.</li>
<li>Develop inspection, qualification, or validation protocols under short timelines.</li>
<li><b>Prioritize critical tasks</b> efficiently in a fast-paced and regulated environment.</li>
<li>Collaborate cross-functionally and communicate effectively with internal stakeholders.</li>
<li>Demonstrate strong negotiation and problem-solving skills when dealing with quality issues.</li>
</ul>Minimum Requirements<br>
One of the following combinations is required:
<ul><li>Doctorate degree in a scientific field or</li>
<li>Master&rsquo;s degree with a minimum of 2 years of directly related experience or</li>
<li>Bachelor&rsquo;s degree with a minimum of 4 years of directly related experience
</li><li>Field of Study
<ul><li>Scientific background in Science or Engineering</li>
</ul></li><li>Experience in the Pharmaceutical Industry, preferably within Quality Control laboratories</li>
<li>Background or experience as Microbiologist, Chemist, Biochemist, Molecular Scientist, or Chemical Engineer</li>
<li>Experience with laboratory testing, method validation, method transfer, and quality processes</li>
</ul>Required Skills and Competencies
<ul><li>Strong technical writing skills (English/Spanish)</li>
<li>Excellent communication and interpersonal skills</li>
<li>Strong organizational and time management skills</li>
<li>Ability to manage multiple priorities and meet deadlines</li>
<li>High attention to detail and commitment to quality and compliance</li>
<li>Ability to work independently and as part of a multidisciplinary team</li>
</ul>This Company is an equal employment opportunity employer. We adhere to a policy of making employment decisions without regard to race, color, religion, sex, sexual orientation, national origin, citizenship, age or disability. We assure you that your opportunity for employment with this Company depends solely on your qualifications.</div>

Specialist Quality Control - 35191

KAUST (King Abdullah University of Science and Technology)

<div>
 <p>
  <strong>
   The Role
  </strong>
 </p>
 <p>
  <br/>
 </p>
 <p>
  The Research Compliance Specialist is responsible for creating, developing, implementing, and promoting the Research Data Management (RDM) Program at KAUST. RDM training and management provide the foundation for the preservation, protection, and monetization of one of KAUST&rsquo;s most valuable resources (research data).
 </p>
 <p>
  <br/>
 </p>
 <p>
  KAUST is an internationally respected research institution, and its reputation is dependent upon the good data management practices of its researchers.
 </p>
 <p>
  <br/>
 </p>
 <p>
  A state-of-the-art RDM program developed and implemented by the Research Compliance Specialist will ensure that the University conducts research that meets or exceeds national and international RDM standards. By enabling the reuse of data and rationalizing resource allocation, RDM supports both research excellence and the optimization of operating costs. In addition, the reputation of the University is impacted by the RDM practices that its graduates and postdoctoral researchers take with them when they leave the University.
 </p>
 <p>
  The Research Compliance Specialist will ensure that the University&rsquo;s students and postdoctoral
 </p>
 <p>
  researchers leave KAUST adequately equipped to manage research data.
 </p>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   Responsibilities
  </strong>
 </p>
 <p>
  <br/>
 </p>
 <ul>
  <li>
   Serve as a subject matter expert on research data management (RDM) regulations, guidelines, and best practices.
  </li>
  <li>
   Promote a culture of responsible research data management across KAUST&rsquo;s diverse research environment.
  </li>
  <li>
   Analyze existing RDM systems and processes, identifying gaps and opportunities for integration.
  </li>
  <li>
   Develop and implement policies governing RDM at the University.
  </li>
  <li>
   Design, deploy, and manage RDM tools or solutions tailored to KAUST&rsquo;s needs.
  </li>
  <li>
   Coordinate and consolidate existing guidance, resources, and efforts across departments.
  </li>
  <li>
   Benchmark with external institutions and stakeholders to identify RDM best practices.
  </li>
  <li>
   Prepare guidance documents, online resources, and web content to support RDM practices.
  </li>
  <li>
   Provide strategic advice to stakeholders on implementing effective RDM practices.
  </li>
  <li>
   Develop course curricula and deliver training sessions, workshops, and presentations on RDM.
  </li>
  <li>
   Engage with faculty, staff, students, and administrators to foster compliance and awareness.
  </li>
  <li>
   Monitor, audit, and evaluate the effectiveness of the RDM program.
  </li>
  <li>
   Assist with investigations or enquiries related to alleged RDM mismanagement.
  </li>
  <li>
   Perform day-to-day administrative duties associated with the RDM program.
  </li>
  <li>
   Provide administrative support to other compliance programs, including: Animal Care and Use, Biosafety, Human Subjects Research, Radiation Safety, Scientific Diving, and Responsible Conduct of Research Programs.
  </li>
  <li>
   Be cross-trained and able to assist colleagues in the support of the above programs.
  </li>
  <li>
   Supplement administration of Research Compliance and RCR activities.
  </li>
  <li>
   Transcribing notes, minutes, and formal proceedings.
  </li>
  <li>
   Other duties as assigned.
  </li>
 </ul>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   Qualifications
  </strong>
 </p>
 <p>
  <br/>
 </p>
 <ul>
  <li>
   Doctoral or master&rsquo;s degree in a regulatory, scientific or related field.
  </li>
 </ul>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   Required Skills
  </strong>
 </p>
 <p>
  <br/>
 </p>
 <ul>
  <li>
   6+ years of research data management experience within a scientific or related environment.
  </li>
  <li>
   Experience with RDM program administration is preferred.
  </li>
  <li>
   Customer-driven approach.
  </li>
  <li>
   Demonstrated expertise in RDM practices.
  </li>
  <li>
   Proactive and self-driven.
  </li>
  <li>
   Strong organizational skills.
  </li>
  <li>
   Collaborative nature with strong persuasive skills.
  </li>
  <li>
   A firm understanding of scientific practices and research methods.
  </li>
  <li>
   Knowledge of organizational and administrative support processes.
  </li>
  <li>
   Strong verbal and written communication skills.
  </li>
  <li>
   Demonstrated proficiency with computer applications.
  </li>
  <li>
   Excellent verbal, written communication, and presentation skills.
  </li>
  <li>
   High degree of confidentiality.
  </li>
 </ul>
 <p>
 </p>
</div>


Research Data Management Compliance Specialist

Meet Life Sciences

<div>
 <p>
  <strong>
   Field-Based | Dubai, UAE
  </strong>
 </p>
 <p>
  <br/>
 </p>
 <p>
  I&rsquo;m currently supporting a
  <strong>
   pharmaceutical client
  </strong>
  with the search for several
  <strong>
   Medical Science Liaison (MSL) &ndash; Oncology
  </strong>
  hires in
  <strong>
   Dubai, UAE
  </strong>
  .
 </p>
 <p>
  <br/>
 </p>
 <p>
  This is a field-based opportunity for scientifically strong medical professionals who enjoy building credible relationships with external experts and supporting high-quality scientific exchange across oncology products spanning both
  <strong>
   marketed and pipeline assets
  </strong>
  .
 </p>
 <p>
  Working closely with global and local cross-functional teams, these individuals will act as trusted scientific partners to
  <strong>
   oncologists, haematologists, investigators, and other key stakeholders
  </strong>
  across their assigned regions. The roles will focus on
  <strong>
   non-promotional scientific engagement, insight gathering, and support for evidence-generation activities
  </strong>
  , while ensuring all work is delivered compliantly and in line with local regulations.
 </p>
 <p>
  <br/>
 </p>
 <p>
  Key responsibilities
 </p>
 <ul>
  <li>
   Identify, map, and develop scientific relationships with
   <strong>
    key opinion leaders, investigators, and cancer centres
   </strong>
   across the assigned territory
  </li>
  <li>
   Deliver
   <strong>
    high-quality, balanced, non-promotional scientific exchange
   </strong>
   with healthcare professionals across the oncology landscape
  </li>
  <li>
   Gather and share
   <strong>
    field medical insights
   </strong>
   to help inform local and global medical strategy
  </li>
  <li>
   Support the planning and execution of
   <strong>
    advisory boards, medical education programmes, and scientific discussions
   </strong>
  </li>
  <li>
   Contribute to
   <strong>
    evidence-generation initiatives
   </strong>
   , including investigator-initiated studies, real-world evidence activities, and company-sponsored research
  </li>
  <li>
   Maintain up-to-date knowledge of
   <strong>
    disease areas, treatment pathways, clinical data, competitive activity, and local treatment guidelines
   </strong>
  </li>
  <li>
   Provide scientific input and training to relevant
   <strong>
    internal cross-functional stakeholders
   </strong>
  </li>
  <li>
   Attend
   <strong>
    regional and local congresses / scientific meetings
   </strong>
   to stay current on emerging data and evolving standards of care
  </li>
  <li>
   Respond to
   <strong>
    unsolicited medical information requests
   </strong>
   in a timely, accurate, and compliant manner
  </li>
  <li>
   Ensure all activities are carried out in line with
   <strong>
    internal procedures, local regulations, and applicable codes of conduct
   </strong>
  </li>
 </ul>
 <p>
  <br/>
 </p>
 <p>
  External stakeholder exposure
 </p>
 <ul>
  <li>
   Oncologists
  </li>
  <li>
   Haematologists
  </li>
  <li>
   Allied Healthcare Professionals
  </li>
  <li>
   National and Regional KOLs
  </li>
  <li>
   Investigators and Academic Institutions
  </li>
  <li>
   Oncology Societies and Co-operative Groups
  </li>
  <li>
   Patient Advocacy Groups
  </li>
  <li>
   CROs and external partners
  </li>
 </ul>
 <p>
  <br/>
 </p>
 <p>
  Ideal background
 </p>
 <p>
  I&rsquo;d be keen to speak with candidates who bring:
 </p>
 <ul>
  <li>
   Previous experience in an
   <strong>
    MSL or field medical role
   </strong>
  </li>
  <li>
   Strong scientific understanding of
   <strong>
    oncology
   </strong>
   , with haematology exposure also of interest
  </li>
  <li>
   Experience engaging with
   <strong>
    KOLs, investigators, and specialist healthcare professionals
   </strong>
  </li>
  <li>
   A strong grounding in
   <strong>
    medical affairs
   </strong>
   and compliant scientific communication
  </li>
  <li>
   The ability to interpret and communicate
   <strong>
    clinical data
   </strong>
   clearly and credibly
  </li>
  <li>
   Strong relationship-building and cross-functional collaboration skills
  </li>
  <li>
   A proactive approach and willingness to travel across the assigned region
  </li>
 </ul>
 <p>
  <br/>
 </p>
 <p>
  If this could be of interest, get in touch for a confidential discussion or send me your cv at kenneth.ubaldo@meetlifesciences.com
 </p>
 <p>
 </p>
</div>


Medical Science Liaison (Oncology)

Boston Scientific

<div><p><b>Additional Location(s):</b> N/A</p><p><b>
Diversity - Innovation - Caring - Global Collaboration - Winning Spirit - High Performance</b></p><p>
At Boston Scientific, we&rsquo;ll give you the opportunity to harness all that&rsquo;s within you by working in teams of diverse and high-performing employees, tackling some of the most important health industry challenges. With access to the latest tools, information and training, we&rsquo;ll help you in advancing your skills and career. Here, you&rsquo;ll be supported in progressing &ndash; whatever your ambitions.</p><div><p>
Interested in hearing from an Electrophysiology Mapping Specialist at Boston Scientific? Check out our video featuring Gianna to learn more about the role.</p></div><p></p><div><p><b><br>
About the role:</b><br>
Now is an exciting time to join our Cardiology team as we launch groundbreaking solutions in the Electrophysiology (EP) market&mdash;one of the fastest-growing areas in med tech. Boston Scientific offers a comprehensive portfolio to treat atrial fibrillation (AFib), including Cryo, Radiofrequency, and Pulsed Field Ablation therapy (FARAPULSE&trade;).</p></div><p></p><div><p><br>
Our technologies encompass 3D Mapping and Navigation systems, Radiofrequency Ablation catheters, Diagnostic Catheters, EP recording systems, and Intracardiac Access Sheaths to diagnose and treat heart rhythm disorders.</p></div><p></p><div><p><br>
In this field-based role, the Electrophysiology Mapping Specialist will begin with an intensive training and development program to gain in-depth knowledge of our technologies and prepare for success. Upon completion, the specialist will provide expert clinical, technical, and educational support to physicians, EP Lab staff, and sales representatives during cardiac procedures using the Opal HDx&trade; mapping system within a defined territory&mdash;contributing directly to patient care and business objectives.</p></div><p></p><div><p><b><br>
Your responsibilities will include:</b></p></div><div><ul><li><p><b>
Maintaining advanced clinical knowledge</b> of EP diagnostic and ablation technologies, PFA, mapping and recording systems, transeptal access tools, and left atrial appendage occlusion technologies I add</p></li></ul></div><div><ul><li><p><b>
Attending procedures in cardiac CV/EP labs</b> to provide clinical support on Boston Scientific AF Solutions products, including the Opal HDx&trade; mapping system, FARAPULSE&trade;, transeptal access tools, diagnostic and therapeutic catheters, and WATCHMAN FLX&trade; devices</p></li></ul></div><div><ul><li><p><b>
Educating customers</b> on clinical usage and benefits of AF Solutions products through customized presentations, demonstrations, and ongoing training</p></li></ul></div><div><ul><li><p><b>
Meeting with physicians and clinical stakeholders</b> to assess their needs and demonstrate how Boston Scientific products support optimal patient outcomes</p></li></ul></div><div><ul><li><p><b>
Developing relationships</b> with hospital staff, physicians, and administrators to expand influence across departments and facilitate strategic decision-making</p></li></ul></div><div><ul><li><p><b>
Responding to clinical and technical inquiries</b> by collaborating across functions including sales, clinical research, marketing, and technical support</p></li></ul></div><div><ul><li><p><b>
Demonstrating change leadership</b> and collaborating cross-functionally to align local activities with broader strategic goals</p></li></ul></div><div><ul><li><p><b>
Implementing strategies outlined in quarterly action plans</b> and coordinating efforts with sales teams to advance business objectives</p></li></ul></div><div><ul><li><p><b>
Supporting physician education and market development</b> by engaging referring physicians, fellows, and key opinion leaders</p></li></ul></div><div><ul><li><p><b>
Training on and adhering to clinical trial protocols and compliance standards</b> in line with global regulatory expectations</p></li></ul></div><div><ul><li><p><b>
Managing clinical trial activity within the territory</b><b>,</b> including Interest Visits and Site Initiation Visits, and educating investigators on study procedures and products</p></li></ul></div><p></p><div><p><b><br>
Required qualifications:</b></p></div><div><ul><li><p>
Bachelor&rsquo;s degree or equivalent experience</p></li></ul></div><div><ul><li><p>
Minimum of 2 years of industry experience in medical device sales, clinical electrophysiology, or equivalent background</p></li></ul></div><div><ul><li><p>
Demonstrated technical aptitude with the ability to convey complex product details clearly</p></li></ul></div><p></p><div><p><b><br>
Preferred qualifications:</b></p></div><div><ul><li><p>
NASPE/IBHRE CEPS certification</p></li></ul></div><div><ul><li><p>
Experience in atrial fibrillation, cardiac mapping, or structural heart procedures</p></li></ul></div><div><ul><li><p>
Familiarity with 3D cardiac mapping systems</p></li></ul></div><p></p><p><b><br>
Requisition ID: </b>626469</p><p></p><p><br>
The anticipated annualized base amount or range for this full time position will be <b>$65,000 to $85,000</b>, plus variable compensation governed by the Sales Incentive Compensation Plan (which includes certain annual non-discretionary incentives based on predetermined objectives) as well as the value of core and optional benefits offered at BSC, which can be reviewed at www.bscbenefitsconnect.com. Actual compensation will be commensurate with demonstrable level of experience and training, pertinent education including licensure and certifications, and other relevant business or organizational needs.</p><p></p><p><b><br>
For MA positions:</b> It is unlawful to require or administer a lie detector test for employment. Violators are subject to criminal penalties and civil liability.</p><p><br>
Boston Scientific transforms lives through innovative medical technologies that improve the health of patients around the world. As a global medical technology leader for more than 45 years, we advance science for life by providing a broad range of high-performance solutions that address unmet patient needs and reduce the cost of healthcare. Our portfolio of devices and therapies helps physicians diagnose and treat complex cardiovascular, respiratory, digestive, oncological, neurological and urological diseases and conditions. Learn more at www.bostonscientific.com and follow us on LinkedIn.</p><p></p><p><br>
Boston Scientific maintains a prohibited substance free workplace. Pursuant to Va. Code &sect; 2.2-4312 (2000), Boston Scientific is providing notification that the unlawful manufacture, sale, distribution, dispensation, possession, or use of a controlled substance or marijuana is prohibited in the workplace and that violations will result in disciplinary action up to and including termination.</p><p></p><p><br>
Please be advised that certain US based positions, including without limitation field sales and service positions that call on hospitals and/or health care centers, require acceptable proof of COVID-19 vaccination status. Candidates will be notified during the interview and selection process if the role(s) for which they have applied require proof of vaccination as a condition of employment. Boston Scientific continues to evaluate its policies and protocols regarding the COVID-19 vaccine and will comply with all applicable state and federal law and healthcare credentialing requirements. As employees of the Company, you will be expected to meet the ongoing requirements for your roles, including any new requirements, should the Company&rsquo;s policies or protocols change with regard to COVID-19 vaccination.</p><p></p><p><br>
Among other requirements, Boston Scientific maintains specific prohibited substance testing requirements for safety-sensitive positions. This role is deemed safety-sensitive and, as such, candidates will be subject to a drug test as a pre-employment requirement. The goal of the drug testing is to increase workplace safety in compliance with the applicable law.</p></div>

EP Mapping Specialist II - Ft. Lauderdale, FL

<div><p><b>Additional Location(s):</b> N/A</p><p><b>
Diversity - Innovation - Caring - Global Collaboration - Winning Spirit - High Performance</b></p><p>
At Boston Scientific, we&rsquo;ll give you the opportunity to harness all that&rsquo;s within you by working in teams of diverse and high-performing employees, tackling some of the most important health industry challenges. With access to the latest tools, information and training, we&rsquo;ll help you in advancing your skills and career. Here, you&rsquo;ll be supported in progressing &ndash; whatever your ambitions.</p><p></p><div><div><p><br>
Interested in hearing from an Electrophysiology Mapping Specialist at Boston Scientific? Check out our video featuring Gianna to learn more about the role.</p></div><p></p><div><p><b><br>
About the role</b>:<br>
Now is an exciting time to join our Cardiology team as we launch groundbreaking solutions in the Electrophysiology (EP) market&mdash;one of the fastest-growing areas in med tech. Boston Scientific offers a comprehensive portfolio to treat atrial fibrillation (AFib), including Cryo, Radiofrequency, and Pulsed Field Ablation therapy (FARAPULSE&trade;).</p></div><p></p><div><p><br>
Our technologies encompass 3D Mapping and Navigation systems, Radiofrequency Ablation catheters, Diagnostic Catheters, EP recording systems, and Intracardiac Access Sheaths to diagnose and treat heart rhythm disorders.</p></div><p></p><div><p><br>
In this field-based role, the Electrophysiology Mapping Specialist will begin with an intensive training and development program to gain in-depth knowledge of our technologies and prepare for success. Upon completion, the specialist will provide expert clinical, technical, and educational support to physicians, EP Lab staff, and sales representatives during cardiac procedures using the Opal HDx&trade; mapping system within a defined territory&mdash;contributing directly to patient care and business objectives.</p></div><p></p><div><p><b><br>
Your responsibilities will include:</b></p></div><div><ul><li><p>
Maintaining advanced clinical knowledge of EP diagnostic and ablation technologies, PFA, mapping and recording systems, transeptal access tools, and left atrial appendage occlusion technologies</p></li></ul></div><div><ul><li><p>
Attending procedures in cardiac CV/EP labs to provide clinical support on Boston Scientific AF Solutions products, including the Opal HDx&trade; mapping system, FARAPULSE&trade;, transeptal access tools, diagnostic and therapeutic catheters, and WATCHMAN FLX&trade; devices</p></li></ul></div></div><div><div><ul><li><p>
Educating customers on clinical usage and benefits of AF Solutions products through customized presentations, demonstrations, and ongoing training</p></li></ul></div><div><ul><li><p>
Meeting with physicians and clinical stakeholders to assess their needs and demonstrate how Boston Scientific products support optimal patient outcomes</p></li></ul></div><div><ul><li><p>
Developing relationships with hospital staff, physicians, and administrators to expand influence across departments and facilitate strategic decision-making</p></li></ul></div><div><ul><li><p>
Responding to clinical and technical inquiries by collaborating across functions including sales, clinical research, marketing, and technical support</p></li></ul></div><div><ul><li><p>
Demonstrating change leadership and collaborating cross-functionally to align local activities with broader strategic goals</p></li></ul></div><div><ul><li><p>
Implementing strategies outlined in quarterly action plans and coordinating efforts with sales teams to advance business objectives</p></li></ul></div><div><ul><li><p>
Supporting physician education and market development by engaging referring physicians, fellows, and key opinion leaders</p></li></ul></div><div><ul><li><p>
Training on and adhering to clinical trial protocols and compliance standards in line with global regulatory expectations</p></li></ul></div><div><ul><li><p>
Managing clinical trial activity within the territory, including Interest Visits and Site Initiation Visits, and educating investigators on study procedures and products</p></li></ul></div><p></p><div><p><b><br>
Required qualifications:</b></p></div><div><ul><li><p>
Minimum of a bachelor&rsquo;s degree or equivalent experience.</p></li></ul></div><div><ul><li><p>
Minimum of 4 years of 3D cardiac mapping system experience or minimum of 8 years in medical device sales, clinical electrophysiology or equivalent education and experience.</p></li></ul></div><div><ul><li><p>
Must demonstrate technical aptitude, and ability to discuss &amp; explain complex technical product information.</p></li></ul></div><p></p><div><p><b><br>
Preferred qualifications:</b></p></div><div><ul><li><p>
NASPE/IBHRE CEPS certification.</p></li></ul></div><div><ul><li><p>
Degree in Biomedical or Mechanical Engineering</p></li></ul></div><div><ul><li><p>
Work experience in Atrial Fibrillation/Cardiac Mapping/Structural Heart Procedure.</p></li></ul></div><div><ul><li><p>
Existing usage of 3D cardiac mapping system.</p></li></ul></div></div><div><div><ul><li><p>
MS or advanced degree in business or healthcare</p></li></ul></div></div><p></p><p><b><br>
Requisition ID: </b>626449</p><p></p><p><br>
The anticipated annualized base amount or range for this full time position will be <b>$</b><b>70,000</b><b> to $</b><b>105,000</b>, plus variable compensation governed by the Sales Incentive Compensation Plan (which includes certain annual non-discretionary incentives based on predetermined objectives) as well as the value of core and optional benefits offered at BSC, which can be reviewed at www.bscbenefitsconnect.com. Actual compensation will be commensurate with demonstrable level of experience and training, pertinent education including licensure and certifications, and other relevant business or organizational needs.</p><p></p><p><b><br>
For MA positions:</b> It is unlawful to require or administer a lie detector test for employment. Violators are subject to criminal penalties and civil liability.</p><p><br>
Boston Scientific transforms lives through innovative medical technologies that improve the health of patients around the world. As a global medical technology leader for more than 45 years, we advance science for life by providing a broad range of high-performance solutions that address unmet patient needs and reduce the cost of healthcare. Our portfolio of devices and therapies helps physicians diagnose and treat complex cardiovascular, respiratory, digestive, oncological, neurological and urological diseases and conditions. Learn more at www.bostonscientific.com and follow us on LinkedIn.</p><p></p><p><br>
Boston Scientific maintains a prohibited substance free workplace. Pursuant to Va. Code &sect; 2.2-4312 (2000), Boston Scientific is providing notification that the unlawful manufacture, sale, distribution, dispensation, possession, or use of a controlled substance or marijuana is prohibited in the workplace and that violations will result in disciplinary action up to and including termination.</p><p></p><p><br>
Please be advised that certain US based positions, including without limitation field sales and service positions that call on hospitals and/or health care centers, require acceptable proof of COVID-19 vaccination status. Candidates will be notified during the interview and selection process if the role(s) for which they have applied require proof of vaccination as a condition of employment. Boston Scientific continues to evaluate its policies and protocols regarding the COVID-19 vaccine and will comply with all applicable state and federal law and healthcare credentialing requirements. As employees of the Company, you will be expected to meet the ongoing requirements for your roles, including any new requirements, should the Company&rsquo;s policies or protocols change with regard to COVID-19 vaccination.</p><p></p><p><br>
Among other requirements, Boston Scientific maintains specific prohibited substance testing requirements for safety-sensitive positions. This role is deemed safety-sensitive and, as such, candidates will be subject to a drug test as a pre-employment requirement. The goal of the drug testing is to increase workplace safety in compliance with the applicable law.</p></div>

EP Senior Mapping Specialist - Phoenix, AZ

<div><p><b>Additional Location(s):</b> N/A</p><p><b>
Diversity - Innovation - Caring - Global Collaboration - Winning Spirit - High Performance</b></p><p>
At Boston Scientific, we&rsquo;ll give you the opportunity to harness all that&rsquo;s within you by working in teams of diverse and high-performing employees, tackling some of the most important health industry challenges. With access to the latest tools, information and training, we&rsquo;ll help you in advancing your skills and career. Here, you&rsquo;ll be supported in progressing &ndash; whatever your ambitions.</p><div><div><p>
Interested in hearing from an Electrophysiology Mapping Specialist at Boston Scientific? Check out our video featuring Gianna to learn more about the role.</p></div><p></p><div><p><b><br>
About the role:</b><br>
Now is an exciting time to join our Cardiology team as we launch groundbreaking solutions in the Electrophysiology (EP) market&mdash;one of the fastest-growing areas in med tech. Boston Scientific offers a comprehensive portfolio to treat atrial fibrillation (AFib), including Cryo, Radiofrequency, and Pulsed Field Ablation therapy (FARAPULSE&trade;).</p></div><div><p>
Our technologies encompass 3D Mapping and Navigation systems, Radiofrequency Ablation catheters, Diagnostic Catheters, EP recording systems, and Intracardiac Access Sheaths to diagnose and treat heart rhythm disorders.</p></div><div><p>
In this field-based role, the Electrophysiology Mapping Specialist will begin with an intensive training and development program to gain in-depth knowledge of our technologies and prepare for success. Upon completion, the specialist will provide expert clinical, technical, and educational support to physicians, EP Lab staff, and sales representatives during cardiac procedures using the Opal HDx&trade; mapping system within a defined territory&mdash;contributing directly to patient care and business objectives.</p></div><p></p><div><p><b><br>
Your responsibilities will include:</b></p></div><div><ul><li><p>
Maintaining advanced clinical knowledge of EP diagnostic and ablation technologies, PFA, mapping and recording systems, transeptal access tools, and left atrial appendage occlusion technologies I add</p></li></ul></div><div><ul><li><p>
Attending procedures in cardiac CV/EP labs to provide clinical support on Boston Scientific AF Solutions products, including the Opal HDx&trade; mapping system, FARAPULSE&trade;, transeptal access tools, diagnostic and therapeutic catheters, and WATCHMAN FLX&trade; devices</p></li></ul></div><div><ul><li><p>
Educating customers on clinical usage and benefits of AF Solutions products through customized presentations, demonstrations, and ongoing training</p></li></ul></div><div><ul><li><p>
Meeting with physicians and clinical stakeholders to assess their needs and demonstrate how Boston Scientific products support optimal patient outcomes</p></li></ul></div><div><ul><li><p>
Developing relationships with hospital staff, physicians, and administrators to expand influence across departments and facilitate strategic decision-making</p></li></ul></div><div><ul><li><p>
Responding to clinical and technical inquiries by collaborating across functions including sales, clinical research, marketing, and technical support</p></li></ul></div><div><ul><li><p>
Demonstrating change leadership and collaborating cross-functionally to align local activities with broader strategic goals</p></li></ul></div><div><ul><li><p>
Implementing strategies outlined in quarterly action plans and coordinating efforts with sales teams to advance business objectives</p></li></ul></div><div><ul><li><p>
Supporting physician education and market development by engaging referring physicians, fellows, and key opinion leaders</p></li></ul></div><div><ul><li><p>
Training on and adhering to clinical trial protocols and compliance standards in line with global regulatory expectations</p></li></ul></div><div><ul><li><p>
Managing clinical trial activity within the territory, including Interest Visits and Site Initiation Visits, and educating investigators on study procedures and products</p></li></ul></div></div><p></p><div><div><p><b><br>
Required Qualifications:</b></p></div><div><ul><li><p>
Bachelor&rsquo;s degree (or equivalent experience).</p></li></ul></div><div><ul><li><p>
Minimum of 6 years of 3D cardiac mapping system experience or minimum of 10 years in medical device sales, clinical electrophysiology or equivalent education and experience.</p></li></ul></div><div><ul><li><p>
Must demonstrate technical aptitude, and ability to discuss &amp; explain complex technical product information.</p></li></ul></div><p></p><div><p><b><br>
Preferred Qualifications:</b></p></div><div><ul><li><p>
NASPE/IBHRE CEPS certification.</p></li></ul></div><div><ul><li><p>
Work experience in Atrial Fibrillation/Cardiac Mapping/Structural Heart Procedure.</p></li></ul></div><div><ul><li><p>
Existing usage of 3D cardiac mapping system.</p></li></ul></div><div><ul><li><p>
MS or advanced degree in business or healthcare.</p></li></ul></div></div><p></p><p><b><br>
Requisition ID: </b>626470</p><p></p><p><br>
The anticipated annualized base amount or range for this full time position will be <b>$80,000 to $120,000</b>, plus variable compensation governed by the Sales Incentive Compensation Plan (which includes certain annual non-discretionary incentives based on predetermined objectives) as well as the value of core and optional benefits offered at BSC, which can be reviewed at www.bscbenefitsconnect.com. Actual compensation will be commensurate with demonstrable level of experience and training, pertinent education including licensure and certifications, and other relevant business or organizational needs.</p><p></p><p><b><br>
For MA positions:</b> It is unlawful to require or administer a lie detector test for employment. Violators are subject to criminal penalties and civil liability.</p><p><br>
Boston Scientific transforms lives through innovative medical technologies that improve the health of patients around the world. As a global medical technology leader for more than 45 years, we advance science for life by providing a broad range of high-performance solutions that address unmet patient needs and reduce the cost of healthcare. Our portfolio of devices and therapies helps physicians diagnose and treat complex cardiovascular, respiratory, digestive, oncological, neurological and urological diseases and conditions. Learn more at www.bostonscientific.com and follow us on LinkedIn.</p><p></p><p><br>
Boston Scientific maintains a prohibited substance free workplace. Pursuant to Va. Code &sect; 2.2-4312 (2000), Boston Scientific is providing notification that the unlawful manufacture, sale, distribution, dispensation, possession, or use of a controlled substance or marijuana is prohibited in the workplace and that violations will result in disciplinary action up to and including termination.</p><p></p><p><br>
Please be advised that certain US based positions, including without limitation field sales and service positions that call on hospitals and/or health care centers, require acceptable proof of COVID-19 vaccination status. Candidates will be notified during the interview and selection process if the role(s) for which they have applied require proof of vaccination as a condition of employment. Boston Scientific continues to evaluate its policies and protocols regarding the COVID-19 vaccine and will comply with all applicable state and federal law and healthcare credentialing requirements. As employees of the Company, you will be expected to meet the ongoing requirements for your roles, including any new requirements, should the Company&rsquo;s policies or protocols change with regard to COVID-19 vaccination.</p><p></p><p><br>
Among other requirements, Boston Scientific maintains specific prohibited substance testing requirements for safety-sensitive positions. This role is deemed safety-sensitive and, as such, candidates will be subject to a drug test as a pre-employment requirement. The goal of the drug testing is to increase workplace safety in compliance with the applicable law.</p></div>

EP Principal Mapping Specialist - Baltimore, MD

AbbVie

<div><b>Company Description</b><p><br>
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas &ndash; immunology, oncology, neuroscience, and eye care &ndash; and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on X, Facebook, Instagram, YouTube, LinkedIn and Tik Tok.</p><b><br>
Job Description</b><p><b><br>
Affiliate:</b></p><p><b>
Gulf Levant
</b></p><p><b>Title:</b></p><p><b>
Medical Advisor &ndash; Gastroenterology
</b></p><p><b>Reporting to:</b></p><p><b>
Medical Manager &ndash; Immunology
</b></p><p><b>PRIMARY FUNCTION:
</b></p><p>Represent the affiliate&rsquo;s medical/scientific voice of expertise for assigned product(s) and relevant therapeutic area(s). Provide medical / scientific expert advice / guidance to key customers for assigned product(s) and relevant therapeutic area(s), including scientific exchange and professional relationship development with External Experts (EEs). Provide medical / scientific input into Medical Affairs strategies for the affiliate medical department and commercial plans, as required, and medical / scientific support for medical department activities under the overall direction of the Affiliate Medical Director. Provide medical affairs support to cross-functional affiliate teams. Ensure that the medical affairs role is fully integrated to support the strategy and execution of affiliate business, while being functionally independent.</p><p><b>
RESPONSIBILITIES:</b></p><ul><li>
Being an active brand team member to support overall strategy and execution. Provide medical/scientific input into marketing strategy and key commercial initiatives, as required.</li><li>
Develop and maintain in-depth knowledge for assigned product(s) / relevant therapeutic area(s) through attendance / participation at key internal meetings/training sessions, relevant congresses, and seminars and by regular self-study of the national/area literature.</li><li>
Provide expert medical/scientific advice for assigned products and related therapeutic areas, including responding to requests for scientific/technical information; contribute to the development and medical and scientific accuracy of core dossiers generated by the medical department (i.e., pricing and reimbursement dossiers, HEOR dossiers, medical information packs, clinical expert reviews etc.).</li><li>
Establish and maintain professional and credible relationships with External Experts (EEs) and academic centers; this will involve participating in scientific congresses, coordinating advisory boards, round-table meetings, discussion forums etc.</li><li>
Deliver scientific presentations and medical education programs to healthcare professionals individually or in groups (meetings, clinical sessions, etc.), where appropriate.</li><li>
Screen relevant literature and other information from relevant scientific societies meetings and conferences and develop summaries of key messages for use within the company (e.g. key areas of scientific/company interest, new trends in diagnosis, monitoring and treatments in the therapeutic area, etc.)</li><li>
Deliver training to sales forces and other departments; develop and update relevant training materials.</li><li>
Clinical Research Activities:<ul><li>
Design and implement clinical research projects within defined standards and budgets (e.g., Phase IV, post marketing clinical activities such as registry/database projects, epidemiological surveys, and PMOS studies).</li><li>
Provide the required oversight to manage review, approval and conduct of IIS studies.</li><li>
Support the affiliate Clinical Research Department in the management of clinical studies, as appropriate (e.g., review new clinical study protocols, identifying potential investigators/sites, conducting feasibility surveys).</li></ul></li><li>
Review and preparation of promotional / non-promotional material. Ensure the medical/scientific content is correct, balanced fair and fully compliant with AbbVie&rsquo;s internal policies and guidelines and in accordance with local laws.</li><li>
Ensure compliance with all applicable national laws and regulations, guidelines, codes of conduct, AbbVie&rsquo;s policies and procedures and accepted standards of best practice.</li><li>
Provide input, as required, into the development of product or TA specific strategic medical affairs plans for the affiliate medical department and local commercial plans; collaborate and partner with local business partners to ensure that medical activities for assigned products / therapeutic areas are aligned with local business-related strategic plans.</li><li>
Ensure adherence to all applicable national laws and regulations, guidelines, codes of conduct, AbbVie standards, policies, and procedures.</li><li>
Operate as a scientific interface and resource to HCPs/Customer(s), Health Care Institutions, External Experts, and professional associations regarding assigned AbbVie Products or Products in Development.</li><li>
Provide specialist medical/scientific strategic input and operational support of core activities such as local clinical research, HCP/Customer interactions, generation and communication of clinical and scientific data, educational initiatives, and patient safety for assigned products / therapeutic areas.</li></ul><p></p><p><b><br>
INTERNAL / EXTERNAL CONTACTS AND INTERACTIONS:</b></p><ul><li>
In-Field/Brand Team members (as applicable)</li><li>
Affiliate R&amp;D personnel: Medical Director, Medical operation and Evidence Generation Specialist, Medical Managers/Advisors; Medical Information team / specialists; affiliate pharmacovigilance / drug safety personnel (as applicable)</li><li>
Marketing and Sales of assigned product and therapeutic area; Market access teams; Affiliate Brand teams.</li><li>
Affiliate Government Affairs; Affiliate Public Affairs; Regulatory Affairs; Legal; OEC.</li><li>
Area and HQ based Therapeutic Area medical affairs teams.</li><li>
Area Medical Affairs teams</li><li>
Medical Directors and Clinical Teams within Clinical Development Operations and Global Medical Affairs.</li><li>
Healthcare personnel (including physicians, nurses, pharmacists).</li><li>
Participating Research Investigators; thought leaders/external experts.</li><li>
Institutions and Scientific or Medical Societies.</li><li>
Hospitals, other healthcare providers, payers, and Local Regulatory Authorities.</li></ul><p><b>
LOCATION:</b></p><p>
This function is hybrid in nature. Typically, up to 50% of an individual&rsquo;s time may be spent working in the field.</p><p></p><b><br>
Qualifications</b><br>
<ul><li>
Advanced degree (e.g. PharmD., PharmB., MD, PhD) in a relevant scientific discipline is preferred but candidates with an undergraduate degree in a relevant discipline and demonstrated experience will be considered</li><li>
Solid knowledge of the pharmaceutical environment and the role of Medical Affairs to advance the medical and scientific objectives of a pharmaceutical company.</li><li>
Prior experience in Medical Affairs is required.</li><li>
Demonstrated expertise in the scientific methods applied to clinical research and current legislative/regulatory controls applicable to this research.</li><li>
Ability to comprehensively learn about new subject areas and environments.</li><li>
Excellent written and spoken communication and presentation skills, with a demonstrated ability to develop and maintain strong collaborative relationships with thought leaders, physicians, and other healthcare decision makers.</li><li>
A good understanding of written and oral English is mandatory.</li><li>
Collaborative, team-oriented approach, able to develop and support relationships across an organization as well as with key external stakeholders and the healthcare community at large.</li><li>
Experience being an active contributor to cross-functional teams and/or working in matrix organizations will be an advantage.</li><li>
Works independently: limited guidance/oversight. Works broadly across functions to facilitate and support the affiliate&rsquo;s medical and clinical activities as necessary.</li><li>
Sound judgment, strong planning and organizational skills, and the ability to get things done. Demonstrated strong sense of urgency.</li><li>
High customer orientation and high digital savviness skills.</li><li>
Strong commitment to compliance with the relevant rules and procedures, and to scientific quality and integrity</li><li>
Ability to travel regularly (approximately 50%)</li></ul><br>
<b>
Additional Information</b><div></div><p><br>
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.</p><p>
US &amp; Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html</p><p>
US &amp; Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:</p><p>
https://www.abbvie.com/join-us/reasonable-accommodations.html</p></div>

Medical Advisor Immunology – Gastroenterology Gulf

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