medical advisor

Boehringer Ingelheim

<div><p><b>The Opportunity<br>
</b></p><p></p><p>We are seeking a highly motivated and scientifically driven <b>Medical Advisor </b>to join our Medical Affairs team in Riyadh, Saudi Arabia. This role is instrumental in shaping medical strategy, driving scientific exchange, and supporting the success of our specialty care and rare disease portfolio.<br>
</p><p></p><p>This position reports to the Medical Affairs Manager.<br>
<br>
<br>
<br>
<br>
<b>Role &amp; Responsibilities<br>
</b></p><p></p><ul><li>Implement and execute short- and long-term medical goals and tactics, with an emphasis on pharmacotherapeutic aspects and with an understanding of business priorities.
</li><li>Act as health care manager responsible for health care compliance revision and approval of commercial communication.
</li><li>Provide scientific leadership in cross-functional TA Brand team and contribute to the country strategy for brand medical plans.
</li><li>Provide expert medical and scientific support to internal stakeholders and external healthcare professionals.
</li><li>Develop and execute medical plans aligned with brand strategy.
</li><li>Analyze and interpret clinical research, scientific literature, and complex data sets to inform decision-making.
</li><li>Support real-world data generation initiatives and contribute to evidence-based strategies.
</li><li>Engage with key opinion leaders (KOLs) and HCPs to foster scientific dialogue and gather insights.
</li><li>Collaborate cross-functionally with regulatory, market access, and commercial teams.
</li>Ensure compliance with local regulations, company policies, and ethical standards.<br>
<li>
</li></ul><p></p><p><b>Requirements<br>
</b></p><p></p><ul><li>Medical degree (MD, PharmD, or PhD in life sciences).
</li><li>Minimum of 3 years of experience in Medical Affairs within a pharmaceutical company
</li><li>Previous relevant experience within KSA is preferred
</li><li>Proven experience in specialty care and/or rare diseases.
</li><li>Strong ability to analyze and interpret clinical research and complex scientific data.
</li><li>Experience in real-world data generation and evidence-based medical initiatives.
</li><li>Excellent communication, presentation, and interpersonal skills.
</li>Business fluent in English; business fluent in Arabic is a plus.<br>
<li>
</li></ul><p></p><p><b>What&rsquo;s Next?
</b></p><p>We are looking forward to receiving your application! We will then have a look at your profile. If we see a match, we will invite you for a screening interview.<br>
</p><p></p><p><b>Screening:
</b></p><p>To comply with applicable export control laws, Boehringer Ingelheim periodically screens business relations (including job applicants) against sanctioned party lists (&ldquo;SPL&rdquo;). These checks may be performed by Boehringer Ingelheim or by any of its Affiliates. You acknowledge that Boehringer Ingelheim and/or its Affiliates will screen you against SPL and that for this purpose your personal data may be processed in relevant databases, including databases of third-party vendors that perform SPL screening for or on behalf of Boehringer Ingelheim or its Affiliates which may be located or accessible outside the EU. Boehringer Ingelheim is committed to ensuring an adequate level of protection of your personal data.</p></div><p></p>

Medical Advisor

<div><p>Job Description</p><p></p><p>
Title: Medical Advisor &ndash; Hematology
</p><p>Location: Riyadh or Jeddah, Saudi Arabia
</p><p>Department: Medical Affairs
</p><p>Reporting to: Therapy Area Lead</p><p>
Role Summary: The Medical Advisor (MA) &ndash; Hematology provides scientific and clinical leadership for the hematology portfolio in Saudi Arabia, ensuring compliant medical strategy execution, evidence generation, external expert engagement, and cross-functional support aligned with SFDA and company policies.</p><p></p><p>
Key Responsibilities:</p><ul><li><p>
Medical Strategy and Planning:</p></li></ul><p>
Develop and execute the KSA hematology medical plan aligned to brand strategy and local market needs. Identify scientific gaps and medical education needs, feed insights into brand planning and lifecycle management.</p><p>
Execution of 70% field-based interactions.</p><ul><li><p>
External Expert Engagement:</p></li></ul><p>
Build and maintain peer-to-peer relationships with KOLs, academic centers, and professional societies across hematology.</p><p>
Conduct fair, balanced scientific exchange, capture insights, and translate them into actionable plans.</p><p>
Support advisory boards, speaker programs, and scientific roundtables in full compliance.</p><ul><li><p>
Evidence Generation and Data Dissemination:</p></li></ul><p>
Lead/support local research (IIS/ISR, RWE, registries, non-interventional studies) and collaborate on regional/global trials.</p><p>
Partner with Clinical Operations on feasibility, site identification, and medical oversight in KSA.</p><p>
Interpret and present clinical data; contribute to publication plans and scientific communications.</p><p>
Collaborate on HEOR/RWE projects relevant to access, guidelines, and reimbursement.</p><ul><li><p>
Medical Information and Scientific Support:</p></li></ul><p>
Provide timely, accurate, balanced medical information; handle unsolicited requests compliantly.</p><p>
Train CFT teams on disease area, product science, and competitive landscape.</p><p>
Review and approve promotional and non-promotional materials per SFDA and internal SOPs.</p><ul><li><p>
Patient Access and Cross-Functional Collaboration:</p></li></ul><p>
Partner with Market Access on value propositions, evidence needs, and payer engagements.</p><p>
Collaborate with Regulatory on SFDA submissions, labeling, and commitments.</p><p>
Support Pharmacovigilance with medical review of ICSRs and aggregate safety data as needed.</p><ul><li><p>
Medical Education and Congresses:
</p></li></ul><p>Lead CME programs, workshops, tumor boards; coordinate medical presence at national/regional congresses. Ensure scientific booths, symposia, and materials meet ethical and compliance standards.</p><ul><li><p>
Compliance and Governance:</p></li></ul><p>
Adhere to SFDA regulations, Saudi anti-commercial bribery law, industry codes (e.g., IFPMA/PhRMA), and company policies. Maintain high standards of ethics, transparency, and documentation.</p><p></p><p>
Qualifications (Must-have):</p><ul><li><p>
Medical degree (MD/MBBS) or PharmD/PhD in a relevant biomedical field.</p></li><li><p>
Priority Experience in hematology.</p></li><li><p>
Minimum 5years of experience in the pharmaceutical industry.</p></li><li><p>
At least 2 year of experience specifically in Medical Affairs.</p></li><li><p>
Proven ability to interpret and communicate complex clinical/biostatistical data.</p></li><li><p>
Fluency in English; Arabic proficiency strongly preferred.</p></li><li><p>
Residency in Saudi Arabia</p></li></ul><p></p><p>
Preferred</p><ul><li><p>
Experience with evidence generation (IIS/RWE), KOL engagement, and medical material review in KSA.</p></li><li><p>
Familiarity with SFDA regulations, formulary pathways, and hospital procurement in Saudi Arabia.</p></li></ul><p></p><p>
Key Competencies</p><ul><li><p>
Strategic thinking with strong scientific rigor</p></li><li><p>
Clear communication and impactful presentation skills</p></li><li><p>
Stakeholder management and influence without authority</p></li><li><p>
Project management, prioritization, and compliance mindset</p></li><li><p>
Agility, initiative, and problem-solving</p></li></ul><p></p><p>
Travel</p><ul><li><p>
Willingness to travel up to 40&ndash;60% within KSA and occasional GCC &amp; International travel.</p></li></ul><p></p><p>
Employment Type</p><ul><li><p>
Full-time; in Riyadh or Jeddah.</p></li></ul><p></p><p><b>
Required Skills:
</b></p>Data Analysis, Hematology, Medical Affairs, Patient Access, Pharmaceutical Industry, Prioritization, Scientific Communications, Scientific Publications, Stakeholder Management, Strategic Networking<p></p><p><b>
Preferred Skills:
</b></p><p></p><p>Current Employees apply HERE</p><p></p><p>
Current Contingent Workers apply HERE</p><p></p><p><b>
Search Firm Representatives Please Read Carefully</b><br>
Merck &amp; Co., Inc., Rahway, NJ, USA, also known as Merck Sharp &amp; Dohme LLC, Rahway, NJ, USA, 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>
Employee Status:
</b></p>Regular<p></p><p><b>
Relocation:</b></p><p></p><p><b>
VISA Sponsorship:</b></p><p></p><p><b>
Travel Requirements:</b></p><p></p><p><b>
Flexible Work Arrangements:</b></p>
Not Applicable<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>
Job Posting End Date:</b></p>
12/2/2025<ul><li><b>A job posting is effective until 11:59:59PM on the day </b><b>BEFORE</b><b> the listed job posting end date. Please ensure you apply to a job posting no later than the day </b><b>BEFORE</b><b> the job posting end date.<br>
</b></li></ul><br>
<p><b>Requisition ID:</b>R374642</p></div>

Medical Advisor – Hematology

Perseptex

<div>
 <strong>
  Senior Medical Advisor &ndash; Bahrain
 </strong>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   Location:
  </strong>
  Manama, Bahrain
 </p>
 <p>
  <strong>
   Commitment:
  </strong>
  Advisory / Part-Time
 </p>
 <p>
  <strong>
   Compensation:
  </strong>
  Competitive
 </p>
 <p>
  <br/>
 </p>
 <strong>
  Overview
 </strong>
 <p>
  <br/>
 </p>
 <p>
  Perseptex is seeking a highly respected physician to serve as a Senior Medical Advisor in Bahrain. This role is intended for a clinician with strong credibility, deep understanding of healthcare delivery, and a passion for improving clinical efficiency and staff capacity. The Senior Medical Advisor will support evidence-based evaluation of Perseptex&rsquo;s technology, participate in research or case studies, and represent Perseptex at clinical and academic events across Bahrain.
 </p>
 <p>
  <br/>
 </p>
 <p>
  This role focuses on
  <strong>
   clinical insight, thought leadership, and system improvement
  </strong>
  , not commercial sales.
 </p>
 <p>
  <br/>
 </p>
 <strong>
  Responsibilities
 </strong>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   Clinical &amp; Scientific Insight
  </strong>
 </p>
 <p>
  <br/>
 </p>
 <ul>
  <li>
   Contribute to research initiatives, case studies, or clinical evaluations that demonstrate the impact of Perseptex&rsquo;s AI systems.
  </li>
  <li>
   Present findings or educational content at medical conferences, grand rounds, and professional forums.
  </li>
  <li>
   Communicate the clinical relevance and rigor of Perseptex&rsquo;s solutions in an evidence-based, physician-centered way.
  </li>
 </ul>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   Healthcare System Improvement
  </strong>
 </p>
 <p>
  <br/>
 </p>
 <ul>
  <li>
   Advise hospitals and clinics on opportunities to improve workflow efficiency, reduce administrative burden, and enhance staff capacity.
  </li>
  <li>
   Provide clinical perspective on where AI-enabled tools can support care teams, improve quality metrics, or reinforce patient safety.
  </li>
  <li>
   Offer insights into local clinical practices, regulatory expectations, and standards of care in Bahrain.
  </li>
 </ul>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   Strategic Medical Advisory
  </strong>
 </p>
 <p>
  <br/>
 </p>
 <ul>
  <li>
   Guide Perseptex on Bahrain&rsquo;s healthcare priorities, clinical challenges, and operational realities.
  </li>
  <li>
   Support the development of materials that reflect accurate clinical context and resonate with Bahraini clinicians.
  </li>
  <li>
   Ensure all clinical positioning is aligned with ethical, evidence-based practice.
  </li>
 </ul>
 <p>
  <br/>
 </p>
 <strong>
  Qualifications
 </strong>
 <p>
  <br/>
 </p>
 <ul>
  <li>
   Physician (MD/MBBS) with significant clinical experience and professional credibility in Bahrain.
  </li>
  <li>
   Experience presenting at conferences, participating in research, or contributing to clinical improvement initiatives.
  </li>
  <li>
   Strong understanding of clinical workflows, hospital operations, or quality improvement methodologies.
  </li>
  <li>
   <strong>
    Native or near-native Arabic proficiency (required).
   </strong>
  </li>
  <li>
   <strong>
    Fluent English listening ability required; spoken English competency preferred but not required.
   </strong>
  </li>
  <li>
   Clear and articulate communicator with the ability to engage both clinical and administrative audiences.
  </li>
 </ul>
 <p>
  <br/>
 </p>
 <strong>
  Additional Expectations
 </strong>
 <p>
  <br/>
 </p>
 <ul>
  <li>
   Willingness to travel within Bahrain for meetings, conferences, and site visits.
  </li>
  <li>
   Ability to learn Perseptex&rsquo;s technology in depth and translate it into clinically meaningful insights.
  </li>
 </ul>
 <p>
  <br/>
 </p>
 <strong>
  Compensation
 </strong>
 <p>
  <br/>
 </p>
 <p>
  Perseptex offers a
  <strong>
   highly competitive compensation package
  </strong>
  , aligned with the seniority and impact of this advisory role.
 </p>
 <p>
  <br/>
 </p>
 <strong>
  About Perseptex
 </strong>
 <p>
  <br/>
 </p>
 <p>
  Perseptex is a Silicon Valley&ndash;based healthcare technology company founded by former Google engineers and clinical experts. We develop advanced AI systems designed to streamline clinical administration, enhance operational efficiency, and expand healthcare team capacity. Our mission is to enable clinicians and hospitals to deliver safer, more effective care through intelligent automation.
 </p>
</div>


Senior Medical Advisor - Bahrain

Novo Nordisk, Inc.

<div><div><div><div><div><p>Regional Medical Advisor - Ahmedabad
</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>Ahemadabad, Gujarat, IN<br>
</div></div></div></div><div></div><div><div><div><div><div><b>Locations: </b>Ahmedabad</div>
<div><b>
Department: </b>Medical Affairs &amp; Medical Education</div>
<div><b>
Novo Nordisk India Pvt. Ltd.</b></div><br>
<div></div>
<div>
Are you a skilled medical professional with a passion for Medical Affairs and a drive to make a real impact? Join Novo Nordisk as a Regional Medical Advisor and be part of a fast-growing, dynamic team where your expertise will shape strategy and patient care in India. If you excel at building scientific relationships, delivering clinical insights, and implementing medical strategies that influence change, we want to hear from you. Apply now with your latest CV &mdash; your next big career move could start here.</div><div><b><br>
Your New Role</b></div>
<div>
As a Regional Medical Advisor, you will translate Novo Nordisk&rsquo;s medical strategy into impactful local activities for your designated region. You will be the scientific face of the company to healthcare professionals and a key partner to internal teams. Your core responsibilities include:</div>
<ul>
<li>Implement local medical plans: Execute the national Medical Affairs strategy within your region, turning strategic objectives into measurable local activities and timelines.</li>
<li>Build and maintain scientific relationships: Establish, nurture and expand strong, evidence-based relationships with key opinion leaders (KOLs), diabetes specialists and other relevant stakeholders to drive scientific exchange and advocacy for Novo Nordisk&rsquo;s portfolio.</li>
<li>Gather and communicate clinical insights: Actively attend scientific meetings and engage with HCPs to capture clinical needs, practice trends and unmet needs. Synthesize these insights and share timely, actionable feedback with cross-functional internal teams.</li>
<li>Support brand and commercial strategy: Collaborate closely with marketing and sales to sharpen product positioning and promotional tactics. Provide medical input to anticipate market changes and recommend corrective or preventive actions.</li>
<li>Medical education and training: Develop and deliver scientific training and educational activities for physicians, allied HCPs, and internal field and marketing personnel to ensure consistent, compliant medical and product knowledge across the region.</li>
<li>Scientific support to stakeholders: Provide medical advice and support to the brand team and other internal stakeholders on clinical data interpretation, label information, and therapeutic positioning.</li>
<li>Ensure compliance and quality: Conduct all activities in line with local regulations, Novo Nordisk policies, and ethical standards for scientific engagement.</li>
</ul>
<div>This role requires strong clinical credibility, excellent stakeholder engagement skills, and the ability to convert scientific evidence into practical actions that benefit patients and support business goals.</div><br>
<div></div>
<div><b>
Your Skills and Qualifications</b></div>
<div>
To be successful in this role, you should have the following qualifications:</div>
<ul>
<li>Education: MD, MBBS from a recognized institution.</li>
<li>Experience: Minimum 2 years&rsquo; relevant experience in Medical Affairs.</li>
<li>Therapeutic knowledge: Solid understanding of diabetes and related metabolic. disorders, with ability to interpret clinical data and treatment paradigms.</li>
<li>Stakeholder engagement &amp; communication: Proven ability to build relationships with HCPs/KOLs and to communicate complex scientific information clearly, both verbally and in writing.</li>
<li>Analytical &amp; execution skills: Strong clinical judgement and analytical ability, plus demonstrated skills in planning, executing and following up projects with attention to detail.</li>
<li>Personal attributes &amp; compliance: Proactive, collaborative and adaptable mindset, with high ethical standards and commitment to regulatory and company policies.</li>
</ul>
<div>Preferred: prior MSL/Regional Medical Advisor experience or direct experience with diabetes products.</div><br>
<div></div>
<div><b>
Your New Department</b></div>
<div>
The Clinical, Medical, and Regulatory (CMR) department at Novo Nordisk is one of the most diverse and collaborative groups within the organization. From health-care-provider interactions and developing and implementing regulatory strategies with the FDA to providing medical education and collecting data to support efficacy and new product development, CMR is involved. The one thing that keeps us all marching to the same beat is our patient-centered focus. At Novo Nordisk, you will help patients around the world. As their needs evolve, so does our challenge to find better and more innovative ways to improve their quality of life. We&rsquo;re changing lives for living.</div><br>
<div><b>
Working at Novo Nordisk</b></div>
<div>
Every day we seek the solutions that defeat serious chronic diseases. To do this, we</div>
<div>
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><br>
<div></div>
<div><b>
What we offer</b></div>
<div>
There is, of course, more on offer here than the uniqueness of our culture and the extraordinary results we produce. Being part of a global healthcare company means opportunities to learn and develop are all around us, while our benefits are designed with your career and life stage in mind.</div><br>
<div></div>
<div><b>
More Information</b></div>
<div>
To submit your application, please upload your CV and motivational letter online (click on Apply and follow the instructions). Internal candidates are kindly requested to inform their line Managers before applying.</div><br>
<div></div>
<div><b>
Deadline</b></div>
<div>
15 December 2025</div><br>
<div></div>
<div><b><i>
Disclaimer</i></b><br>
<b><i>&quot;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.&quot;</i></b></div>
<div><i>
Also, it has been brought to our attention that there have recently been instances of fraudulent job offers, purporting to be from Novo Nordisk and/or its affiliate companies. The individuals or organizations sending these false employment offers may pose as a Novo Nordisk recruiter or representative and request personal information, purchasing of equipment or funds to further the recruitment process or offer paid trainings. Be advised that Novo Nordisk does not extend unsolicited employment offers. Furthermore, Novo Nordisk does not charge prospective employees with fees or make requests for funding as a part of the recruitment process.</i></div><div></div><div><br>
We commit to an inclusive recruitment process and equality of opportunity for all our job applicants.</div><br>
<div></div>
<div>
We&rsquo;re 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></div></div></div></div>

Regional Medical Advisor - Ahmedabad

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>
PRIMARY FUNCTION:</b><br>
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><br>
<b>
RESPONSIBILITIES:</b><br>
1. 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.<br>
2. 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.<br>
3. 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.).<br>
4. 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.<br>
5. Deliver scientific presentations and medical education programs to healthcare professionals individually or in groups (meetings, clinical sessions, etc.), where appropriate.<br>
6. 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.)<br>
7. Deliver training to sales forces and other departments; develop and update relevant training materials.<br>
<b>8. Clinical Research Activities:</b><br>
a. 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).<br>
b. Provide the required oversight to manage review, approval and conduct of IIS studies.<br>
c. 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).<br>
9. 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.<br>
10. 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.<br>
11. 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.<br>
12. Ensure adherence to all applicable national laws and regulations, guidelines, codes of conduct, AbbVie standards, policies, and procedures.<br>
13. 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.<br>
14. 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.</p><div><br>
<b>
INTERNAL / EXTERNAL CONTACTS AND INTERACTIONS:</b><br>
<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></div><p><br>
<b>
LOCATION:</b></p><p>
Riyadh &amp; or Jeddah<br>
This function is hybrid in nature. Typically, up to 50% of an individual&rsquo;s time may be spent working in the field.</p><b><br>
Qualifications</b><br>
<ul><li>
Minimum 2 years of Medical Affairs experience in a multinational pharmaceutical company</li><li>
Experience in Immunology is an advantage</li><li>
Evidence Generation / Medical Operations exposure is a plus (e.g., PMOS, IIS, registries, RWE projects)</li><li>
Strong learning agility and ability to grow within the TA/Medical Affairs structure</li><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 Local Market Experience</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>
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 Dermatology

Abbott

<div><p><b>MAIN PURPOSE OF ROLE</b></p><p></p><p>
Applies subject matter knowledge in the area of Medical Affairs.</p><p>
Requires capacity to apply skills/knowledge within the context of specific needs or requirements.</p><p></p><p><b>
MAIN RESPONSIBILITIES</b></p><ul><li>
As the Experienced professional in the Medical Affairs Sub-Function, possesses well developed skills in overseeing the direction, planning, execution, clinical trials/research and the data collection activities.</li><li>
Contributes to implementation of clinical protocols, and facilitates completion of final reports.</li><li>
Recruits clinical investigators and negotiates study design and costs.</li><li>
Responsible for directing human clinical trials, phases III &amp; IV for company products under development.</li><li>
Participates in adverse event reporting and safety responsibilities monitoring.</li><li>
Coordinates and provides reporting information for reports submitted to the regulatory agencies.</li><li>
Monitors adherence to protocols and determines study completion.</li><li>
Coordinates and oversees investigator initiations and group studies.</li><li>
May participate in adverse event reporting and safety responsibilities monitoring.</li><li>
May act as consultant/liaison with other corporations when working under licensing agreements.</li></ul><p></p><p><b>
QUALIFICATIONS</b></p><p></p><p><b>
Education</b></p><p>
Associates Degree (&plusmn; 13 years)</p><p></p><p><b>
Experience/Background</b></p><p>
Minimum 1 year</p></div>

Regional Medical Advisor

<div><div><div><div><div><div><div><div><div><div><div><h2 class="jobSectionHeader"><b>Main Purpose of the Role</b></h2></div></div><div></div><div><div><ul><li><div>
Summarize the main purpose of the role</div><div><div><div><div>
Experienced professional individual contributor that works under limited supervision.<br>
Applies subject matter knowledge in the area of Medical Affairs.<br>
Requires capacity to apply skills/knowledge within the context of specific needs or requirements.</div></div></div></div></li></ul></div></div></div></div></div></div></div></div></div></div><div><div><div><div><div><div><div><div><div><div><h2 class="jobSectionHeader"><b>
Main Responsibilities</b></h2></div></div><div></div><div><div><ul><li><div>
List the main responsibilities this role regularly performs.</div><div><div><div><div><ul><li>
As the Experienced professional in the Medical Affairs Sub-Function, possesses well developed skills in overseeing the direction, planning, execution, clinical trials/research and the data collection activities.</li><li>
Contributes to implementation of clinical protocols, and facilitates completion of final reports.</li><li>
Recruits clinical investigators and negotiates study design and costs.</li><li>
Responsible for directing human clinical trials, phases III &amp; IV for company products under development.</li><li>
Participates in adverse event reporting and safety responsibilities monitoring.</li><li>
Coordinates and provides reporting information for reports submitted to the regulatory agencies.</li><li>
Monitors adherence to protocols and determines study completion.</li><li>
Coordinates and oversees investigator initiations and group studies.</li><li>
May participate in adverse event reporting and safety responsibilities monitoring.</li><li>
May act as consultant/liaison with other corporations when working under licensing agreements.</li></ul></div></div></div></div></li></ul></div></div></div></div></div></div></div></div></div></div></div>

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