medical affairs specialist

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

Baylor Miraca Genetics Laboratories LLC

<div><p><b>*** This candidate must reside in Florida, Georgia, South Carolina, or North Carolina</b></p>
<p><b>
Medical Science Liaison</b></p>
<p>
The field-based Medical Affairs team of Medical Science Liaisons (MSLs) at Baylor Genetics play a key role in clinical and scientific education to internal and external parties. The MSL serves as a scientific and clinical expert and liaison between Baylor Genetics and key opinion leaders (KOLs), healthcare professionals, medical associations and academic centers through the development, dissemination and clarification of pertinent scientific and clinical information. Each MSL establishes long-term clinical and science-based relationships with healthcare professionals that help to ensure access to current, accurate and relevant scientific information through the process of education via one-on-one interactions, small group discussions, and presentations at local and national conferences. The MSL will aid other members of the Medical Affairs team in development of scientific content, and the MSL is responsible for organizing and delivering continuing education (CME/CEU) presentations.</p>
<p>
The MSL may also collaborate with various external agencies, consultants, investigators, and collaborators as well as internal stakeholders, including Sales, Customer Support, Business Development, Product, Marketing, and Research/Development. The MSL also serves as an expert resource on Baylor Genetics products and associated disease states.</p>
<p>
MSLs are expected to work closely with the Manager of Medical Affairs and the Science Writer &amp; Content Manager to contribute to multiple abstracts and publications each year. To be successful in this role, this individual will be a strategic thinker with excellent attention to detail, outstanding oral and written communication skills, and a demonstrated ability to communicate complex scientific concepts in a compelling and concise manner to various internal and external stakeholders. This position can be remote.</p>
<p><b>
QUALIFICATIONS AND EXPERIENCE:</b></p>
<ul>
<li>Advanced degree in scientific field required (MS in Genetic Counseling, PhD, NP, MD).</li>
<li>Minimum of 3+ years of clinical experience in pediatric medicine with an emphasis on genetics required. In addition, 2+ years of industry experience in Medical Affairs strongly preferred.</li>
<li> Familiarity with key aspects of genomics and molecular diagnostics technologies.</li>
<li> Proven history delivering high quality scientific presentations.</li>
<li>Proven history of authoring peer-reviewed scientific publications, scientific posters &amp; abstracts.</li>
<li>Fluency with all MS Office and SharePoint software required.</li>
<li>Experience leading initiatives and/or teams cross functionally.</li>
<li> Excellent planning and organizational skills with excellent verbal and written communication skills.</li>
<li>Ability to efficiently manage time and priorities.</li>
<li>Ability to work in a fast-paced environment while working collaboratively on multiple projects with competing priorities.</li>
<li>Demonstrated problem solving skills in a complex and matrixed environment.</li>
<li>Self-driven attitude to take initiative and work independently and collaboratively with minimal supervision towards a common goal.</li>
<li>Ability to read, interpret, and convey complex scientific information to audiences of varying backgrounds.</li>
<li>This position requires 40-50% travel (national and international), including overnight and occasional weekend travel.</li>
<li> Attendance at periodic internal and external meetings which may include national and international locations.</li>
</ul>
<p><b>Duties and Responsibilities:</b></p>
<ul>
<li>Work with a motivated and dynamic Medical Affairs team to provide educational support to healthcare professionals and organizations on Baylor Genetics products and services.</li>
<li> Work with contacts outside of the company including healthcare providers, investigators and collaborators, influential clinicians, KOLs (Key Opinion Leaders), and advisory boards, as appropriate.</li>
<li> Serve as an expert resource on pediatric genetics &amp; genomics and on Baylor Genetics products to provide educational support for the field sales team and other internal partners.</li>
<li> With the broader Medical Affairs team, participate in abstract development and support publication efforts, as well as attend relevant educational meetings and conferences annually.</li>
<li> In collaboration with product marketing and scientific communications, develop multi-channel medical educational activities and tools including illustrative case studies, speaker programs, slide decks, CE events, etc.</li>
<li> Work effectively and collaboratively with internal sales, marketing, and customer support to support sales colleague development through coaching aligned with technical and business opportunities/strengths. Review sales materials for technical accuracy, medical appropriateness and utility to customers and field team.</li>
<li> Deliver effective, high-quality presentations in scientific venues, online webinars, etc.</li>
<li> Monitor and analyze medical literature to inform internal stakeholders of key scientific and competitive developments.</li>
<li> Attend assigned major medical conferences to provide scientific support to the commercial Baylor Genetics team and contribute to a meeting summary report from each conference to summarize key scientific and competitive observations for internal stakeholders.</li>
<li>Lead and contribute to other Medical Affairs projects as needed.</li>
<li> May perform other related duties as required and/or assigned.</li>
</ul>
<p><b>PHYSICAL DEMANDS AND WORK ENVIRONMENT:</b></p>
<ul>
<li>Frequently required to talk or hear.</li>
<li>Frequently required to utilize visual acuity to operate equipment, read technical information, and/or use a keyboard.</li>
<li>Frequently required to sit or stand.</li>
</ul>
<p><b>EEO Statement:</b></p>
<p>
Baylor Genetics is proud to be an equal-opportunity employer dedicated to building an inclusive and diverse workforce. We do not discriminate based on race, religion, color, national origin, sex, sexual orientation, age, gender identity, veteran status, disability, genetic information, pregnancy, childbirth, or related medical conditions, or any other status protected under applicable federal, state, or local law.</p></div><p></p>

Medical Science Liaison- Southeast

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)

Glenmark Pharmaceuticals

<div>
 <p>
  <strong>
   <u>
    Role Overview:
   </u>
  </strong>
 </p>
 <p>
  <br/>
 </p>
 <p>
  The Medical Science Liaison (MSL) &ndash; Oncology is a field-based medical professional responsible for executing Glenmark&rsquo;s medical affairs strategy in the region assigned for oncology products across their lifecycle, including pipeline and marketed assets.
 </p>
 <p>
  <br/>
 </p>
 <p>
  Working in close alignment with Global Medical Affairs and the local cross-functional team, the MSL serves as a scientific expert and trusted partner to oncologists, hematologists, investigators, and other key healthcare stakeholders. The role focuses on high-quality, non-promotional scientific exchange, medical insight generation, and support of evidence generation initiatives, while ensuring full compliance with local regulations, including local regulatory requirements and the Code of Conduct
 </p>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   <u>
    Job Responsibilities:
   </u>
  </strong>
 </p>
 <p>
  <br/>
 </p>
 <ul>
  <li>
   Identifies, maps, and develops scientific relationships with key oncology KOLs, investigators, and cancer centers across regions assigned in alignment with the medical strategy.
  </li>
  <li>
   Conducts high-quality, non-promotional scientific exchange with HCPs, ensuring fair-balanced communication of clinical data, benefits, risks, and appropriate use of Glenmark oncology products.
  </li>
  <li>
   Gathers, analyses, and communicates actionable medical insights from the field to inform local and global medical strategies.
  </li>
  <li>
   Supports planning and execution of medical education initiatives such as advisory boards, medical education programs (MEPs), and focused group discussions.
  </li>
  <li>
   Supports clinical evidence generation activities including investigator-initiated studies, real-world evidence initiatives, and company-sponsored studies in collaboration with Global Medical and Clinical teams.
  </li>
  <li>
   Maintains in-depth knowledge of disease areas, treatment paradigms, competitive landscape, and local treatment guidelines relevant to assigned oncology assets
  </li>
  <li>
   Provides scientific training and medical input to internal stakeholders, including sales and cross-functional teams, ensuring accuracy and compliance.
  </li>
  <li>
   Attends local and regional oncology congresses and scientific meetings to remain current on emerging data and evolving standards of care.
  </li>
  <li>
   Responds to unsolicited medical information requests in a timely, accurate, and compliant manner, in collaboration with Medical Information and PV teams.
  </li>
  <li>
   Ensures all medical activities are conducted in compliance with Glenmark SOPs, health authority regulations, and the local code of conduct
  </li>
 </ul>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   <u>
    Educational Qualifications:
   </u>
  </strong>
 </p>
 <p>
  <br/>
 </p>
 <p>
  Advanced degree in Life Sciences or Healthcare (PharmD, M. Pharm, PhD, Msc, MBBS, BDS or equivalent)
 </p>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   <u>
    Experience:
   </u>
  </strong>
 </p>
 <p>
  <br/>
 </p>
 <p>
  Minimum 2&ndash;4 years of experience as a Medical Science Liaison, preferably in Oncology. Experience engaging with oncology stakeholders within the country healthcare system is strongly preferred. Familiarity with local regulatory requirements, clinical research processes, and medical affairs operations
 </p>
</div>


Medical Science Liaison

Novo Nordisk, Inc.

<div><div><div><div><div><p>Medical Advisor
</p></div></div></div></div><div><div><div><div><b>Category: </b>Medical Affairs
</div></div></div></div><div><div><div><div><b>Location:
</b>Karachi, Sindh, PK<br>
</div></div></div></div><div></div><div><div><div><div><div>Are you a talented and dedicated medical doctor looking for a job in the pharmaceutical industry? Are you passionate about medical science and eager to make a difference in the diabetes community as well as building strong relationships with key stakeholders? If so, we invite you to apply for the position of <b>Medical Advisor</b> at Novo Nordisk Pakistan. Read more and apply today for a life-changing career.</div>
<div><b>
Your new role</b></div>
<div>
As a Medical Advisor at Novo Nordisk, you will play a pivotal role in shaping and executing medical strategies to support our diabetes and obesity portfolios.</div>
<div>
Your responsibilities will be:</div>
<ul><li>Develop and drive the medical strategy to align with and support the overarching brand and business priorities.</li></ul>
<ul><li>Facilitate KOL engagement in trials, identify new sites, conduct site education visits, support investigator-sponsored studies, and develop relationships with Key Opinion Leaders (KOLs) for speaker engagements.</li></ul>
<ul><li>Develop and conduct advisory boards, communicate scientific and clinical data, create and execute publication plans for assigned portfolios, present at national and international conferences, and engage external authors.</li></ul>
<ul><li>Develop and implement the medical education strategy for assigned portfolios; review all commercial-led medical education meetings and accredited medical education; attend conferences and congresses.</li></ul>
<ul><li>Conduct internal training; translate scientific information for internal stakeholders to assist with the development and implementation of strategy; approve promotional material; provide tailored medical responses.</li></ul>
<div><b>
Your new department</b><br>
The Medical Affairs Team at Novo Nordisk Pakistan is based in Karachi and is part of the MRPV (Medical, Regulatory, and Pharmacovigilance) department. We are a dynamic and collaborative team dedicated to ensuring the optimal delivery of scientific information to the medical community. Our mission is to drive medical strategies, support the diabetes and obesity portfolios, and make a meaningful difference in the lives of patients. Working closely with key stakeholders, we foster a fast-paced and innovative environment where your contributions will directly impact our success.</div>
<div><b>
Your skills &amp; qualifications</b><br>
We are looking for candidates who meet the following qualifications:</div>
<ul>
<li>MBBS degree</li>
<li>Minimum 2 years&rsquo; experience in Medical Affairs Department</li>
<li>Advanced English proficiency</li>
<li>Ready for business travel</li>
</ul>
<div><b>Working at Novo Nordisk</b><br>
Every day we seek the solutions that defeat serious chronic diseases. To do this, we approach our work with an unconventional spirit, a rare determination and a constant curiosity. For over 100 years this unordinary mindset has seen us build a company unlike any other. One where a collective passion for our purpose, mutual respect and a willingness to go beyond what we know delivers extraordinary results.</div>
<div><b>
Deadline</b><br>
27.03.2026. Applications are reviewed on an ongoing basis.</div>
<div>
Novo Nordisk is currently in the process of adjusting job titles globally. Please note that the job title listed in this advertisement may be subject to change. More detailed information will be provided during the recruitment process.</div>
<div>
Novo Nordisk is not your typical healthcare company. In a modern world of quick fixes, we focus on solutions to defeat serious chronic diseases and promote long-term health. Our unordinary mindset is at the heart of everything we do. We seek out new ideas and put people first as we push the boundaries of science, make healthcare more accessible, and treat, prevent, and even cure diseases that affect millions of lives. Because it takes an unordinary approach to drive real, lasting change in health.</div><div>
We commit to an inclusive recruitment process and equality of opportunity for all our job applicants.</div><br>
<div></div>
<div>
At Novo Nordisk, we're not chasing quick fixes &ndash; we're creating lasting change for long-term health. For over 100 years, we've been driven by a single purpose: to defeat serious chronic diseases and help millions of people live healthier lives. This dedication fuels our constant curiosity and inspires us to push the boundaries of what's possible in healthcare. We embrace diverse perspectives, seek out bold ideas, and build partnerships rooted in shared purpose. Together, we're making healthcare more accessible, treating and preventing diseases, and pioneering solutions that create change spanning generations. When you join us, you become part of something bigger &ndash; a legacy of impact that reaches far beyond today.</div></div></div></div></div></div>

Medical Advisor

Hikma

<p></p><div><div><div><div><div><div><div>Description:
<p><b>Job</b><br>
<b>Location:</b> Dubai, United Arab Emirates.<br>
<b>Department:</b> Medical Affairs - Biotechnology<br>
<b>Reports to:</b> Associate Director, Medical</p><br>
<p></p>
<p><b>
Job Purpose:</b></p>
<p>
The Sr MSL is a field-based medical expert role focused on developing and maintaining peer-to-peer relationships with key medical experts. This role will primarily support the company biotechnology franchise. The Sr MSL will collaborate with physicians and other medical experts to provide field observations to internal stakeholders and ensure that health care professionals have the most up to date information as the clinical development programs mature this role will be reporting to the MENA Medical Associate Director Biotechnology.</p>
<p>
This is a field-based job with 80% of the time allocated to the field and nearly 20% travel time.</p><br>
<p></p>
<p><b>
Key Responsibilities:</b></p>
<ul>
<li>Develop and maintain peer-to-peer collaborations and relationships with key medical experts in the Biotechnology community.</li>
<li>Develop territory field medical plan and TLs Interaction plans based on therapeutic area objectives and TLs needs.</li>
<li>Support clinical development initiatives including site identification, trial recruitment, registry, and presentation of final approved data.</li>
<li>Collaborate with physicians on medical affairs initiatives including publications, advisory boards, medical education opportunities, training, and speaker development.</li>
<li>Serve as scientific peer-to-peer resource to external disease experts and internal stakeholders.</li>
<li>Support the medical community with up-to-date medical information, robust disease expertise, and product information.</li>
<li>Communicate clinical insights on new data to the company medical Affairs and to inform medical strategy for the assigned therapeutic area.</li>
<li>Train internal &amp; external stakeholders on key scientific and medical topics in relevant therapeutic area.</li>
<li>Maintain effective and appropriate communication among internal stakeholders while maintaining full compliance with relevant requirements.</li>
<li>Generate tactical regional plans to provide needs based, value-added support of the medical and scientific community in-line with company goals.</li>
<li>Uses systems to strategically map, identify, profile, and prioritize thought leaders in line with the medical plan and goals.</li>
<li>Maintain accurate reporting and documentation of MSL activities.</li>
<li>Provide medical and scientific information to respond to KOLs' technical questions about company`s product.</li>
<li>Lead meetings with KOLs to discuss relevant scientific literature and address their enquiries.</li>
<li>Make educational presentations to senior doctors and researchers, for example on clinical trial data.</li>
<li>Feed information back to marketing and sales colleagues to help develop marketing materials and commercial strategy.</li>
<li>Keep up to date with the latest scientific research and clinical data relevant to the company`s molecules.</li>
<li>Share safety information with the pharmacovigilance division.</li>
<li>Comply with all internal &amp; external regulations and codes that apply to medical, regulatory and compliance perspectives.</li>
<li>Support for the development of Medical Plans.</li>
<li>Support for management of clinical studies including Company Investigational Studies (CISs) &amp; Investigator Initiated Studies (IISs).</li>
<li>Supports product pre-launch, launch, and post-launch activities and communication plans within medical strategy and tactical plans.</li></ul><br>
<p></p>
<p><b>
Qualifications &amp; Experience:</b></p>
<ul>
<li>5-8 years of experience in the pharmaceutical industry.</li>
<li>A minimum of 2 years of experience in medical as MSL, Regulatory Affairs and/or Pharmacovigilance is preferred.</li>
<li>Business acumen courses/training is a plus.</li>
<li>Clinical research experience and GCP certification is a plus.</li>
<li>National experience is a Preferred.</li>
<li>Biotech experience is a plus.</li>
<li>Candidates must understand compliance considerations and demonstrate ability to work compliantly in a field-based role, within the medical organization, as well as across the commercial organization.</li>
</ul></div></div></div></div><div><div><div><div>Location:
Sharjah, AE</div></div></div></div></div></div></div><p></p>

Sr. Medical Science Liaison

Organon Pharmaceuticals

<p></p><div><p><b>Job Title</b>: Assoc. Dir, Medical Affairs</p><p></p><p><b>
Location / Site</b>: Cairo</p><p></p><p><b>
The Position
</b></p><p></p><p>The Medical Advisor holds primary responsibility within the country for the development and execution of the Medical Affairs Plans in his/her therapeutic areas under the guidance and supervision of the META Cluster Medical Lead. Additionally, the Medical Advisor provides Medical Affairs therapeutic area support through engaging with Scientific Leaders (SLs) / Key Decision Makers (KDMs), driving scientific initiatives and supporting the field force.</p><p></p><p><b><br>
Responsibilities</b></p><p></p><p><i>
Scientific and Technical Leadership</i></p><p></p><ul><li>Communicate scientific therapy needs credibly, appropriately, and effectively across a variety of internal and external stakeholders at all levels.</li><li>Build trust with the external scientific community via peer-to-peer scientific exchange, research and educational collaborations, interactions with scientific societies and health organizations, publications, etc.</li><li>Provide therapeutic/functional training to assigned teams and affiliate functions.</li><li>Develop and help execute country medical educational programs and symposia.</li><li>Lead country Advisory Boards and Expert Input Forums in line with strategy.</li><li>Participate in and contribute significantly to professional organizations, academic or regulatory working teams.</li><li>Provide scientific inputs for digital initiatives.</li></ul><p></p><p><i>
Medical Strategy and Therapy Leadership</i></p><p></p><ul><li>Translate Global Medical Strategies into research, data analysis, scientific communication, educational, and other tactics and solutions that improve patient outcomes and enhance access in the country.</li><li>Ensure effective communication and collaboration between field and Medical through providing scientific and medical support to the Commercial team.</li><li>Evaluate accuracy of promotional materials.</li><li>Provide Medical Affairs therapeutic area support through engaging with SLs/KDMs, driving scientific initiatives and supporting the field force.</li><li>Collect, analyze, and communicate actionable insights at the country level.</li><li>Provide scientific inputs for digital initiatives.</li><li>Successfully collaborate, provide scientific inputs, and lead resolution of Regulatory queries/issues.</li><li>Support execution of and quickly adapt tactical plans to business realities in country.</li><li>Act with ethics and integrity; Provide non-promotional, balanced, reliable and scientific information.</li><li>Support with therapy training content for Sales team.</li><li>Demonstrate strategic thinking, specifically related to asset value proposition, and clinical and value evidence.</li><li>Support creation of Medical Affairs Plans along with the TA and META cluster Medical Leads.</li></ul><p></p><p>
Medical Information</p><p></p><ul><li>Provide prompt medical information support, such as research and answering of medical inquiries from external and internal customers.</li></ul><p></p><p><b>
Required Education, Experience and Skills</b></p><p><br>
</p><ul><li>Minimum of 4 year's experience in filed medical affairs.</li><li>
Pharma industry experience required, minimum 5 years in multinational company.</li><li>
Medical degree, PhD, Pharm D or other relevant life sciences degree.</li><li>
Ability to communicate knowledge of the therapeutic area, through scientific exchange in different environments and with different stakeholders (one on one, lectures, etc.)</li><li>
Ability of critical lecture of the medical literature related to the therapeutic area</li><li>
Ability to analyze medical literature in order to evaluate the different tendencies in research</li><li>
Strong scientific baseline knowledge in assigned therapeutic area(s).</li><li>
Scientific leadership</li><li>
Ability to communicate knowledge of the therapeutic area, through scientific exchange in different environments and with different stakeholders (one on one, lectures, etc)</li><li>
Ability of critical lecture of the medical literature related to the therapeutic area</li><li>
Demonstrate strategic thinking, specifically related to asset value proposition, and clinical and value evidence</li><li>
Strategic planning</li><li>
High level of scientific and ethical integrity.</li><li>
Excellent communication skills, including listening and probing skills, across a variety of internal and external audiences.</li><li>
Strong collaboration and negotiation skills and ability to function within a team environment.</li><li>
Problem solving</li><li>
Analytical skills</li><li>
Understanding of core systems, tools and metrics related to medical literature</li><li>
Excellent written and oral proficiency in English</li><li>
Complex projects management</li><li>
Candidate must be based in Cairo</li></ul><p></p><p><b>
Secondary Job Description</b></p><p></p><p><b>
Who We Are:
</b></p><p>Organon delivers ingenious health solutions that enable people to live their best lives. We are a $6.5 billion global healthcare company focused on making a world of difference for women, their families and the communities they care for. We have an important portfolio and are growing it by investing in the unmet needs of Women&rsquo;s Health, expanding access to leading biosimilars and touching lives with a diverse and trusted portfolio of health solutions. Our Vision is clear: A better and healthier every day for every woman.</p><p></p><p>
As an equal opportunity employer, we welcome applications from candidates with a diverse background. We are committed to creating an inclusive environment for all our applicants.</p><p></p><p><b>
Search Firm Representatives Please Read Carefully</b><br>
Organon LLC, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails.</p><p></p><p><b>
Annualized Salary Range</b></p><p></p><p><b>
Annualized Salary Range (Global)</b></p><p><b>
Annualized Salary Range (Canada)</b></p><p><b>
Please Note: Pay ranges are specific to local market and therefore vary from country to country.</b></p><p></p><p><b>
Employee Status:
</b></p>Regular<p></p><p><b>
Relocation:</b></p>
No relocation<p></p><p><b>
VISA Sponsorship:</b></p><p></p><p><b>
Travel Requirements: Organon employees must be able to satisfy all applicable travel and credentialing requirements, including associated vaccination prerequisites</b></p><p></p><p><b>
Flexible Work Arrangements:</b></p><p></p><p><b>
Shift:</b></p><p></p><p><b>
Valid Driving License:</b></p><p></p><p><b>
Hazardous Material(s):</b></p><p></p><p><b>
Number of Openings:
</b></p>1<p><b><br>
Requisition ID:</b>R539260</p></div>

Associate Director, Medical Affairs - Egypt

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