Job Title: Medical Advisor Oncology/Hematology (Algeria)
Purpose:
The primary goal of this position is to provide specialist medical/scientific strategic and operational input for Algeria with a focus on oncology/hematology. The role involves core medical affairs activities such as: healthcare professional/provider interactions (Payers Patients Prescribers and Providers) generation of clinical and scientific data enhancing therapeutic benefits and value educational initiatives (medical education data guidelines and value proposition) and safeguarding patient safety (risk minimization activities/safety surveillance activities). The Medical Advisor will collaborate closely with sales marketing and commercial teams to provide strategic medical input into core brand strategies supporting medical/marketing activities (promotional material generation/product launches) and market access.
Responsibilities:
- Provide leadership oversight and support for assigned oncology/hematology products/projects in cooperation with affiliate/Area Medical teams Marketing RA Clinical and other functional areas.
- Establish and approve scientific methods for hypotheses rational design of protocols and interpretation of results.
- Participate in the design and of clinical trial safety product safety and risk management plans. Handle routine and ad hoc safety monitoring reports to regulatory agencies.
- Oversee clinical trials and be medically and scientifically accountable for safety issues and interpretation of statistical analyses for clinical significance.
- Initiate medical affairs activities and disseminate data supporting overall product scientific and business strategy in oncology/hematology.
- Provide scientific/medical education to investigators clinical monitors and project team members related to oncology/hematology.
- Understand and comply with regulatory requirements related to clinical studies and global drug development.
- Act as a medical/scientific leader for oncology/hematology projects within Algeria assisting with the scientific review development approval and communication of medical affairs activities.
- Initiate research projects and drive them to completion resulting in highquality publications.
- Lead crossfunctional subteams responsible for oncology/hematology therapeutic area projects.
Qualifications :
Qualifications:
- Medical Doctorate (M.D. degree or equivalent in relevant therapeutic specialty preferably with completion of residency and/or fellowship.
- Minimum of 2 years of clinical trial or medical affairs experience in oncology/hematology within the pharmaceutical industry or academia. 3 years of experience is preferred along with proven leadership skills in a crossfunctional team environment.
- Expertise in oncology/hematology and knowledge of clinical trial methodology and regulatory requirements previous experience in Eyecare/Neuroscience is a plus.
- Ability to interact externally and internally to support global business strategies. Must possess excellent oral and written English communication skills. Proficiency in local languages relevant to Algeria is preferred.
Additional Information :
Key Stakeholders:
- Healthcare professionals payers patients prescribers providers
- Internal teams: Sales Marketing Regulatory Affairs Clinical and Functional Areas
- External partners: Regulatory agencies medical institutions and research collaborators
AbbVie is an equal opportunity employer and is committed to operating with integrity driving innovation transforming lives serving our community and embracing diversity and inclusion. It is AbbVies policy to employ qualified persons of the greatest ability without discrimination against any employee or applicant for employment because of race color religion national origin age sex (including pregnancy) physical or mental disability medical condition genetic information gender identity or expression sexual orientation marital status status as a protected veteran or any other legally protected group status.
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Work :
No
Employment Type :
Fulltime