Title: Medical Advisor
Duties & Responsibilities:
- Develop and maintain peer-to-peer collaborations and relationships with key medical experts in the Biotechnology community.
- Develop territory field medical plan and TLs Interaction plans based on therapeutic area objectives and TLs needs.
- Support clinical development initiatives including site identification, trial recruitment, registry, and presentation of final approved data.
- Collaborate with physicians on medical affairs initiatives including publications, advisory boards, medical education opportunities, training, and speaker development.
- Serve as scientific peer-to-peer resource to external disease experts and internal stakeholders.
- Support the medical community with up-to-date medical information, robust disease expertise, and product information.
- Communicate clinical insights on new data to the company medical Affairs and to inform medical strategy for the assigned therapeutic area.
- Train internal & external stakeholders on key scientific and medical topics in relevant therapeutic area.
- Maintain effective and appropriate communication among internal stakeholders while maintaining full compliance with relevant requirements.
- Generate tactical regional plans to provide needs based, value-added support of the medical and scientific community in-line with company goals.
- Uses systems to strategically map, identify, profile, and prioritize thought leaders in line with the medical plan and goals.
- Maintain accurate reporting and documentation of MSL activities.
- Provide medical and scientific information to respond to KOLs' technical questions about company`s product.
- Lead meetings with KOLs to discuss relevant scientific literature and address their enquiries.
- Make educational presentations to senior doctors and researchers, for example on clinical trial data.
- Feed information back to marketing and sales colleagues to help develop marketing materials and commercial strategy.
- Keep up to date with the latest scientific research and clinical data relevant to the company`s molecules.
- Share safety information with the pharmacovigilance division.
- Comply with all internal & external regulations and codes that apply to medical, regulatory and compliance perspectives.
- Support for the development of Medical Plans.
- Support for management of clinical studies including Company Investigational Studies (CISs) & Investigator Initiated Studies (IISs).
Supports product pre-launch, launch, and post-launch activities and communication plans within medical strategy and tactical plans.
Education / Qualifications / Skills:
- A medical professional (Physician / Pharmacist) (Male/Female).
- Excellent oral and written communication skills.
- Excellent command of English & Arabic.
- Excellent presentation skills.
- Able to identify local experts and manage local medical activities.
- Mastering computer skills (Microsoft office).
- Problem solving and able to manage complex situations.
- Critical thinking and result oriented personality.
- Proven analytical skills and able to prioritize the assigned tasks.
- Able to work in a team and can identify potential opportunities.
- Share knowledge with other team members.
- Work as part of a team to reach common goals.
- Deliver creative ideas for continuous improvement.
- Develop good relationships with key opinion leaders.
- Energetically embraces responsibilities, demonstrates ability to achieve goals •
- Has strong initiative, and functions well as part of a cross-functional team •
- Exhibits excellent time management •
- Demonstrated ability to work independently •
Must be pro-active team player, flexible, and ability to work in ambiguous situations.
Experience:
- Minimum 2-3 years of experience in pharmaceutical industry with preferred immunology & oncology experience.
- Professional experience in Medical, Regulatory Affairs and/or Pharmacovigilance is preferred.
- Business acumen courses/training is a plus.
- Clinical research experience and GCP certification is a plus.
- Biotech experience is a plus.
- National experience is preferred.
- Candidate 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.
- CV must be in English
Casablanca, MA