medical advisor

Ferring Pharmaceuticals, Inc.

<div><div>Job Description:</div><div>
Roles &amp; Responsibilities<br>
<ul><li>You will be responsible for serving as a core scientific member of the cross-functional franchise team, providing the scientific foundation for the Infertility Division</li></ul></div><ul><li>You will be responsible for conceptualizing and managing a wide range of medical activities, aligned with the TA Medical strategy, including research, publications, medical education, and patient support programs.</li><li>You will be responsible for engaging key thought leaders through medical affairs activities, in line with the overall strategic plan.</li><li>You will be responsible for ensuring the optimal execution of the strategic medical affairs plan through Regional Medical Affairs, encompassing medical education, product education, and special projects.</li><li>You will be responsible for acting as a therapeutic area scientific expert, discussing scientific data with leading specialists, and providing training on the latest medical developments to the sales and marketing team.</li></ul><div>
Qualifications</div><ul><li>
Educational qualification-MBBS with M.D. Pharmacology/Medicine/Obstetrics &amp; Gynecology or full time post-graduate qualification in any discipline of medicine.</li><li>
Minimum work experience- 4-7 years of experience in the pharmaceutical industry or research company in a Medical Advisor capacity.</li></ul><div></div><div><br>
Skills &amp; attributes &ndash;</div><div><br>
Technical Skills</div><ul><li>
Strong academic record with deep knowledge of the therapeutic area, strength in research with knowledge of research methodologies and interpretation of medical data.</li><li>
Strategic mind set with scientific acumen and communication skills in order to be accepted by leading specialists in peer-to-peer relationship is essential.</li><li>
Must have working knowledge of Indian regulations pertaining to Health care professional&rsquo;s interactions (MCI code of ethics for doctors &amp; UCPMP Code for Pharma) and Drugs and Cosmetic Act regulations pertaining to clinical trials and new drug approvals.</li><li>
Experience with complex business environments preferred.</li><li>
Training in medical writing, clinical trial methodologies, research design and ICH &ndash; GCP will be added advantage.</li><li>
Working knowledge of MS Word, powerpoint &amp; excel.</li><li>
Strong track record of success as demonstrated through annual performance ratings and/or professional accomplishments and awards<br>
</li><li>
Behavioural Skills<br>
<ul><li>Integrity driven decision making skills</li><li>Sound scientific knowledge</li><li>Collaboration and teaming with ability to work in a matrix environment</li><li>Strategic thinking &amp; sound analytical skills</li><li>Intellectual curiosity</li><li>Self-awareness and adaptability to work in a matrix environment</li><li>Result oriented and performance driven</li><li>Excellent interpersonal &amp; communication skills to effectively interact with a broad range of audience</li></ul></li></ul><div>
Location:</div>
Ferring India M&amp;S</div>

Medical Advisor/ Senior Medical Advisor

International SOS

<div>
 <strong>
  About The Role
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 <strong>
  Overall Purpose Of The Job (Brief description of the primary purpose of this position)
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 The Medical Advisor is responsible for maintaining, researching, compiling, and writing of International SOS medical content for our clients, as part of a global team on a 7 day per week basis.
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  Key Responsibilities
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  <li>
   Responsible for high quality Medical Alerts (and other dynamic information) published or shared with client facing teams without undue delay
  </li>
  <li>
   Performance of high quality research, including global health threats, pandemic-related information, infectious disease outbreaks and travel vaccinations.
  </li>
  <li>
   Maintenance of Location Guide information as per schedule.
  </li>
  <li>
   Researching, writing and reviewing content for International SOS as per requirement
  </li>
  <li>
   Liasion with different departments including Security, Assistance, Sales, Medical services and others to facilitate functional processes of MInA
  </li>
  <li>
   Active team member with good communication with management and rest of the team.
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  About You
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  <br/>
 </strong>
 <strong>
  Required Skills and Knowledge (Brief description of technical knowledge or skills needed to perform the job)
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Medical Degree from a recognised Medical College
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Required Competencies (Critical behaviors necessary to successfully perform the job)
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 </strong>
 <strong>
  Essential
  <br/>
  <br/>
 </strong>
 &squf; High quality communication skills and cultural sensitivity
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 &squf; Strong work ethic
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 &squf; English &ndash; written and spoken
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 &squf; High quality editing skills
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 &squf; High level of computer literacy
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 &squf; Ability to establish and develop relationships with key stakeholders
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  Preferred
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 </strong>
 &squf; Proficiency in one or more foreign language
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 &squf; Formal epidemiology training
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 &squf; Author of academic publicationsTravel medicine experience
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 &squf; Experience in researching, publishing and maintaining medical information for websites and digital platforms
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 <strong>
  Required Work Experience (Brief description of the job-related experience needed to perform the job)
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 </strong>
 <ul>
  <li>
   Doctors with 3 years of experience or more after graduation
  </li>
  <li>
   Some clinical (or non-clinical) research
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  </li>
 </ul>
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  Required Qualifications (Brief description of the educational background needed to perform the job)
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  <li>
   Medical Doctor - MBBS or equivalent
  </li>
  <li>
   Current license with Indian Medical Council (IMC)
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  Required Languages (Brief description of the language skills needed to perform the job)
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   Excellent Written English
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   Extremely high level of written English, including spelling, grammar and the ability to tailor writing style to particular audiences.
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  </li>
 </ul>
 Travel / Rotation Requirements (Brief description of any travel or rotation requirements)
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   May need to travel occasionally within or outside of country whenever there is a requirement.
  </li>
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</div>


Medical Advisor

productlife group

<div><div><div><div><p>We are looking for a Team lead/ Manager/ senior medical advisor/reviewer proficient in all aspects of clinical and post-marketing drug safety.</p>
</div></div><div><h2 class="jobSectionHeader"><b>Responsibilities:</b></h2>
<div><p>Clinical Phase:</p>
<ul>
<li>Lead as a medical monitor/Medical expert</li>
<li>Medical Monitoring experience is a must and the ability to effectively communicate with the clients, attend investigator meetings as required and provide support to sites regarding protocol or possible drug interactions is essential.</li>
<li>Review and provide feedback on study protocols as needed.</li>
<li>Deliver therapeutic area training for all case processing team.</li>
<li>May require 24/7 availability depending on the client needs for possible queries or protocol deviations resulting in potential harm to patients.</li>
<li>Drafting medical monitoring plans (MMP) and ensuring compliance.</li>
<li>Reviewing adverse events (AEs) reported by study sites, assessing their severity, and determining appropriate actions (like dose adjustments or trial discontinuation).</li>
<li>Make assessments on SUSAR reportability.</li>
<li>Perform the review and interpret clinical data, ensure protocol compliance and draft monthly reports for the clients (with presentation at periodic meetings if required).</li>
<li>Develop and update current training materials in line with GCP and GVP requirements for medical review of all cases.</li>
</ul>
<p>Post-Marketing (Pharmacovigilance):</p>
<ul>
<li>Lead the medical reviewers</li>
<li>Medical review of the ICSRs (Spontaneous, literature)</li>
<li>Support in causality, medical assessment, benefit-risk evaluation of the medicinal product.</li>
<li>Mentor junior medical reviewers and perform additional review of cases to ensure competency.</li>
<li>Provide feedback and ongoing workshops to develop the medical reviewers.</li>
<li>Participate in audits and inspections as required</li>
<li>Ensure understanding of client needs, conventions and ensure expectations are met and exceeded</li>
<li>Training and mentoring other team members</li>
</ul></div></div><div><h2 class="jobSectionHeader"><b>Required Education:</b></h2>
<div><p>MBBS, or MD (Doctor of Medicine)</p><br>
<p></p>
</div></div><div><h2 class="jobSectionHeader"><b>Required Experience :</b></h2>
<div><ul><li>Experience in leading medical review teams</li>
<li>Client communications</li>
<li>Safety Database experience</li>
<li>Minimum 10 years experience working for service providers or pharmaceutical company</li>
<li>At least 5-7 years of experience as a Medical Monitor or clinical phase</li>
</ul></div></div><div><h2 class="jobSectionHeader"><b>Required Technical Skills:</b></h2>
<div><ul><li>Microsoft package</li>
<li>Pharmaceutical background &ndash; strong understanding of GVP, GCP, FDA and regulatory requirements related to drug safety.</li>
<li>Deep knowledge of pharmacovigilance principles, adverse event reporting, causality assessment.</li>
<li>Working knowledge of EDC systems</li>
<li>Good Medical knowledge and Pharmacology understanding</li></ul></div></div></div></div>

Medical Advisor – VAF

Bristol Myers Squibb

<div><b>Working with Us</b><br>
Challenging. Meaningful. Life-changing. Those aren't words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You'll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible.<br>
<br>
Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: careers.bms.com/working-with-us .<br>
<br>
<b>Job Summary:</b><br>
<br>
Senior Medical Advisors (SMA) embody our medical mission in becoming a trusted, agile partner who engages in influential dialogue and delivers timely, high impact data and insights that advance the science or accelerate access, shape medical practice and drive appropriate adoption of BMS medicines.<br>
<br>
The SMA role is a blend of field-based and office-based time; the proportion depending on the life cycle for the compound/therapeutic area of responsibility. It is anticipated that a SMA fulfilling their internal and external duties will also spending time in the field with external customers. SMAs will perform their activities in an ethical and compliant manner, in adherence with all BMS policies and external laws and regulations. The SMA is responsible to actively engage with Thought Leaders and to serve as the Therapeutic Area (TA) reference point within their geographic scope. The SMA is responsible to design, develop and deliver the medical plan in collaboration with cross-functional partners. Participate actively in price and reimbursement prework, discussions, negotiations with government bodies in the different therapeutic areas based on the collaboration with the local partners. Support the development Brand Strategies in collaboration with BMS commercial and cross-functional teams, by communicating medical insight and knowledge about the product or disease area, in particular with reference to patients' needs and treatment trends.<br>
<br>
SMA is also responsible to lead and develop the MSLs as the direct reports.<br>
<br>
<b>Key Responsibilities:</b><br>
<br>
<b>External Environment and Customer Focus:
</b><ul><li>Develop and maintain strong relationships with top thought leaders (TL) and access stakeholders. SMAs will use various channels for interactions (1:1, group presentation; remote, etc).</li><li>
Effectively present information to TLs, as appropriate, ensuring medical accuracy and compliance with local procedures, ethical and legal guidelines and directives.</li><li>
Actively profile the medical landscape and continuously update knowledge and expertise in products, patient treatment trends, unmet medical needs, clinical trials and scientific activities. Understand the competitive landscape and actively prepare to address informational needs of customers.</li><li>
Collect and provide meaningful medical insights back to the medical and commercial organizations to be actioned in support of the strategy development.</li><li>
Role model in developing and maintaining peer to-peer relationships and close contacts with TLs.</li></ul><b>
Manage/Lead MSLs and Deliver the Medical Plan:</b><ul><li>
Provide strategic input into the development of brand plans, develop and execute local medical plan and TL interaction plans.</li><li>
Deliver scientifically meaningful medical program proposals and ensure flawless execution of medical activities</li><li>
Identify potential speakers for BMS educational programs and ensure that these speakers receive all necessary product and disease state training.</li><li>
Deliver scientifically meaningful medical programs proposals and ensure flawless execution of medical activities to support overarching medical plan execution.</li><li>
Discuss and deliver Health Economics and Outcomes Research (HEOR) evidence-based information reactively (ie, to government agencies, healthcare organizations, and payers), as appropriate.</li><li>
Lead cross functional collaboration within matrix teams to ensure appropriate embedding of the medical perspective and aligned focus in key critical execution to achieve overall medical strategies and objectives.</li><li>
Represent medical as a key reference point for internal stakeholders</li><li>
Manage/lead and develop the MSLs in his/her reporting line.</li></ul><b>
Provide Medical Support:</b><ul><li>
Contribute to the development and review of medical content within promotional and nonpromotional materials (as appropriate, consistent with the promotional and non-promotional BMS procedural documents and/or local codes), according to local resource and requirement.</li><li>
Contribute to and coordinate the development of the medical / scientific sections of pricing and reimbursement files.</li><li>
Contribute to the development of scientific publications or presentations, as appropriate.</li><li>
As necessary and appropriate, may support the initial and ongoing medical/scientific area and product specific training and provide key scientific updates to internal stakeholders (Commercial, Regulatory, OR, PV, Legal, HEOR, Market Access, etc).</li></ul><b>
Support Clinical Trial Activities:</b><ul><li>
Support interventional and non-interventional research (NIR) studies (including input on study feasibility, identification and assessment of potential study sites, facilitate BMS and investigator activities, and conduct site visits to support patient recruitment and/or discussions around the safe and effective use of BMS investigational products, as appropriate and in agreement with local medical management.</li><li>
Provide recommendations and insights on study and site feasibilities within the therapeutic area based on knowledge of the field and through direct contacts with potential investigators, as appropriate and in agreement with local medical management.</li><li>
Ensure that BMS Pharmacovigilance procedural documents are understood and applied by investigators of local studies, and alert appropriate BMS personnel to any identified adverse events.</li></ul><b>
Preferred Qualifications:</b><ul><li>
Medical doctor/Pharmacist, with experience in oncology or with a broad medical background from a pharmaceutical company.</li></ul><b>
Experience and Knowledge:</b><ul><li>
People/team management in a pharmaceutical company.</li><li>
At least 3 years of experience in medical affairs function in a pharma company.</li><li>
Fluency in Turkish and English</li></ul>
If you come across a role that intrigues you but doesn't perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.
<br>
<br>
<b>Uniquely Interesting Work, Life-changing Careers</b><br>
With a single vision as inspiring as Transforming patients' lives through science&trade; , every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting global participation in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.<br>
<br>
<b>On-site Protocol</b><br>
<br>
BMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:
<br>
<br>
Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.
<br>
<br>
BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to adastaffingsupport@bms.com . Visit careers.bms.com/ eeo -accessibility to access our complete Equal Employment Opportunity statement.
<br>
<br>
BMS cares about your well-being and the well-being of our staff, customers, patients, and communities. As a result, the Company strongly recommends that all employees be fully vaccinated for Covid-19 and keep up to date with Covid-19 boosters.
<br>
<br>
BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.<br>
<br>
If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: https://careers.bms.com/california-residents/
<br>
<br>
Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.</div>

Senior Medical Advisor

Cellsave Arabia

<p>We are looking for a <b>Female Medical Representative</b> with Medical background.</p><p>You will be handling customer's education about our product, services and converting them into sales.</p><p>You will be responsible for meeting doctors.</p><p>You will be entering customer's data and information.</p><p>An active person with great communication and negotiation skills is essential Arabic and English speaking candidate is a must.</p><p>Job Type: Full-time</p><p>Required education:</p><ul><li>Bachelor's</li></ul><p>Required experience:</p><ul><li>Medical Sales: 1-2 years</li></ul><p>Required languages:</p><ul><li>English</li><li>Arabic</li></ul><p>Required license or certification:</p><ul><li>UAE Driver's License</li></ul><p>Immediate joiners preferred.</p><p>Job Types: Full-time, Permanent</p>

Female Medical Advisor (Abu Dhabi)

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></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><br>
<p></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: Jeddah/Riyadh</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><b>
Prior experience in Medical Affairs is a must with a minimum of 2 years.</b></li><li><b>
Prior experience in solid tumors and companion diagnostics CDx is a must.</b></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>
An excellent 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 - Oncology Solid Tumors (Based in Jeddah or Riyadh)

IQVIA

<div><p>Job Overview
<br>
The objective of this position is to provide medical expertise in the evaluation of safety data from a variety of sources as part of the overall pharmacovigilance process and determine the medical and scientific relevance of serious adverse event reports within the context of the product&rsquo;s safety profile as well as other products within the same therapeutic area. Also, this position plays a greater role as a senior technical leader and participate in matrix management activities including preparation or participation in evaluating safety issues and preparation of aggregate reports in collaboration with the Post-Marketing Safety Experts and Safety Surveillance Group and be responsible for surveillance activities for selected products.
</p><div>Essential Functions
<br>
<ul><li>Perform medical review and clarification of trial-related Adverse Events (AEs) and post-marketing adverse drug reactions (ADRs) including narrative content, queries, coding, expectedness, seriousness, causality and company summary
</li><li>Compose, edit and medically review Analyses of Similar Events (AOSE) for expedited cases as appropriate based on regulatory requirements
</li><li>Provide coding review of AEs, SAEs, SADRs, Past medical history, Concomitant medications or other medical data listings to verify and medically vet clinical data
</li><li>Serve as an internal consultant to pharmacovigilance case processing teams on projects being supported
</li><li>Perform medical safety review of the protocol, Investigative Brochure, and/or Case Report Forms (CRFs) for appropriate safety content and data capture, as applicable
</li><li>Provide aggregate reviews of safety information, including but not limited to clinical data, postmarketing, literature review and observational studies to maintain oversight of a product&rsquo;s safety profile (e.g: DSUR, RMP, PBRER, ad hoc regulatory reports etc)
</li><li>Ensure service delivery from productivity, compliance and quality perspective within regulatory /contracted timelines. Lead and participate in the initiatives taken for the same from team delivery perspective
</li><li>Provide therapeutic area/pharmacovigilance issue guidance in the context of leading/managing other safety team members in single case assessment.
</li><li>Ensure update of watch list, list of expectednsess, labeling list/RSIs etc for the assigned products and develop such additional capabilities within the team
</li><li>Lead, drive and participate in training activities, product transitions, audit preparation and knowledge exchange initiatives
</li><li>Review and sign off on the Project Safety Plan and Medical Monitoring Plan per medical safety scope agreed in contract, as applicable
</li><li>Attend project meetings, medical safety team meetings, and represent safety and clinical data review findings during client meetings, as applicable
</li><li>Act as Lead Safety Physician, or additional team support, and/or back up on assigned projects as applicable
</li><li>Provide medical escalation support for medical information and EU Qualified Persons for Pharmacovigilance projects, as applicable
</li><li>24 hour medical support as required on assigned projects
</li><li>Maintain awareness of medical safety-regulatory industry developments
</li><li>Provide support and participate in signal detection efforts, e.g. strategy meetings etc. as applicable
</li></ul></div><div>Qualifications
<br>
<ul><li>Other A medical degree from an accredited and internationally recognized medical school with a curriculum relevant to general medical education. Req
</li><li>Three (3 years) experience practicing clinical medicine after award of medical degree. Graduate, and/or Residency training can qualify for clinical practice experience Req
</li><li>Two (2) years of pharma experience Pref
</li><li>Sound knowledge of Medicine
</li><li>In-depth knowledge of applicable global, regional and local clinical research regulatory requirements; i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
</li><li>Knowledge of Pharmacovigilance- ICSR and Aggregate reports
</li><li>In-depth knowledge of departmental standard operating procedures (SOPs)
</li><li>Skill in use of multiple safety databases
</li><li>Adequate Computer skills, especially Microsoft word, excel &amp; PowerPoint
</li><li>Good communication skills- verbal and written
</li><li>Ability to establish and maintain effective working relationships with managers, co-workers, investigative site staff, clients and regulatory agency representatives
</li><li>Ability to establish and maintain effective working relationships with coworkers, managers and clients
</li><li>A valid medical license, or equivalent, from the country or region in which he/she resides and works Pref
</li></ul></div><p></p><p>IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide . Learn more at https://jobs.iqvia.com</p></div>

Sr. Medical Safety Advisor

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