Clinical Research Physician

At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We’re looking for people who are determined to make life better for people around the world.

**Purpose of the Role**:
The Clinical Research Physician serves as a scientific resource for study teams, departments, and others as needed. The Clinical Research Physician is aware of and ensures that all activities of the medical team _(and direct reports, if applicable) _are in compliance with current local and international regulations, laws, guidance (for example, FDA, ICH, and CPMP etc.), Good Clinical Practices (GCPs), company standards, Lilly policies and procedures, global quality standards, the Principles of Medical Research and activities are aligned with the medical vision.

**Primary Responsibilities**:

- To provide medical expertise in Obesity, specifically across the Lilly Obesity product portfolio, including affiliate, regional and global teams, contributing to medical strategies and brand commercialisation.
- Ensure detailed, current knowledge of the respective Molecule(s) data. And contribute to scientific and medical expertise to develop effective partnerships with relevant functions, including Pricing Reimbursement & Access (PRA), Clinical Operations, Corporate Affairs, Human Resources, Legal, Marketing, Medical Information, Global Product Safety and Training.
- To develop effective partnerships with clinicians, other key influencers and external groups.
- To provide visible leadership to other members of the Medical Department like Medical Affairs Professional (MAP) and Medical Science Liaisons (MSLs) and the broader India business To contribute Medical Education activities which may include business planning, approval and certification of materials and joint working with other Lilly functions.
- Understand and anticipate the scientific information needs of all local/regional customers (payers, patients, health care providers)
- Actively address customer questions in a timely fashion by leading data analyses and new clinical or health outcomes research efforts.
- Contribute to the development of medical strategies to support brand commercialisation activities
- Contribute as a scientific and medical expert to activities and deliverables of the PRA organisation, in particular giving clinical input and insight to develop payer partnership programs and defend the product value.
- Contribute actively on an ongoing basis to the strategic planning for currently marketed brands.
- Offer scientific and creative input, contribute to the development, review, and approval of promotional materials for the brand team.
- Support training of sales representatives, and other medical representatives along with MAPs & MSLs

**Provision of Medical Expertise**
- Ensure detailed, up-to-date knowledge of the data surrounding the respective Molecule(s)
- Input into regulatory submissions and Health Technology Assessments (HTAs)
- Assist Medical Information and Global Product Safety in the affiliate as requested, including out of hours calls
- Drive and take accountability for the process and content of scientific publications
- Provide initial and ongoing disease, product and competitor training for all Lilly employees
- Provide presentation to groups of HCPs and others as determined by business needs
- Participate at an early stage in the production of materials with substantial or critical medical content (e.g. detail aids, clinical slide sets etc.)
- Attendance of relevant internal and external meetings
- Scientific Data Dissemination/Exchange

**Compliance and Education**
- Knowledge of compliance with local laws and regulations, and global policies and procedures, compliance guidelines with respect to data dissemination and interactions with external health care professionals. Review and approve promotional and non-promotional materials in line with the local compliance guidelines.
- Drive the response to challenges from competitors,
- Comply with Good Pharmaceutical Medical Practice, Good Clinical Practices (GCP) and comply with all local laws
- Support the planning of symposia, advisory board and medical meetings
- Support medical information associates in preparation and review of medical letters and other medical information materials.
- Support training of local medical/non-medical personnel - Medical lead for internal training
- Prepare or review scientific information in response to customer questions or media requests
- Support data analysis and the development of slide sets
- Develop and maintain appropriate collaborations and relationships with releva