We are currently partnered with a Global Pharmaceutical Company who are currently looking for a MD, Board Certified Physician focused on Endocrinology to join their office in the Mid – East of North America!

Business/Customer Support:

Understand and anticipate the scientific information needs of local and regional customers, including payers, patients, and healthcare providers. Proactively address their inquiries by leading data analyses and initiating new clinical or health outcomes research.
Collaborate with global Medical Affairs, brand teams, Global Patient Outcomes/Real World Evidence, and other cross-functional teams to develop medical strategies that support brand commercialization, aligning with the local business plan.

Scientific Data Dissemination/Exchange:

Ensure compliance with local laws, regulations, global policies, and guidelines when disseminating data and interacting with external healthcare professionals.
Address unsolicited scientific inquiries from external healthcare professionals in line with established guidelines.
Assist medical information associates in preparing and reviewing medical letters and other related materials.
Establish and maintain relationships with external scientific experts, thought leaders, and the broader medical community at local, national, regional, and potentially international levels.

Clinical Planning & Clinical Research/Trial Execution and Support:

Advocate for the clinical needs of the country or region during the development of clinical strategies, plans, and study protocols by the business unit’s medical leadership.
Review and approve local informed consent documents and risk profiles to ensure clear communication of risks to study participants.
Collaborate with clinical research staff on the design, conduct, and reporting of local clinical trials, including aspects like sample size, patient commitment, timelines, grants, and governance review interactions as needed.
 
Regulatory Support Activities:

Contribute to the development and review of local labeling and modifications in collaboration with global Development, brand teams, regulatory, and legal departments, demonstrating deep knowledge of local labels.
Provide medical expertise to regulatory scientists and participate in advisory committees.
 
Scientific Technical Expertise:

Stay informed about current trends and projections in clinical practice and access within the therapeutic area(s) relevant to the product, both in the near term (1-2 years) and longer-term (3-5 years).
Critically evaluate relevant medical literature, maintain awareness of the status and data from competitive products, and stay updated on medical and scientific developments related to the product.
Serve as a scientific consultant and protocol expert for clinical study team members and other medical personnel.