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Eli Lilly and Company

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3.8

based on 432 Reviews

Video summary

62 Eli Lilly and Company Jobs

Clinical Research Physician (TA Lead)

Eli Lilly and Company

3.8

based on 432 Reviews

2-7 years

Panipat, Yamunanagar, Faridabad + 3 more

1 vacancy

Clinical Research Physician (TA Lead)

Eli Lilly and Company

posted 2mon ago

Job Role Insights

Flexible timing

Key skills for the job

Pharmacy Data Analysis Healthcare Clinical Research Recruitment GCP

+ 3 more

Job Description

To provide medical expertise in Neuroscience (Alzheimer s Disease, Dementia & other conditions), specifically across the Lilly Neuroscience 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 Access 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 relevant professional societies.

Clinical Planning/Clinical Research/Trial Execution and Support

Drive process of India Clinical Trial (CT) selection from the Global and Regional plan
Input into the development of Global and Regional CT plans
Implement, in consultation with the Clinical Operations lead, the Global / Regional CT plan with Quality Speed and Value
Develop and implement a local CT plan. Participate in investigator interaction and site selection, start-ups, site issue resolution and Plan Do Review (PDR) meetings, trial initiation meetings along with MAPs wherever required

External Relations

Identify and engage with Health Care Professionals (HCPs), Advocacy Groups, government and other professional bodies as determined by business needs
Share and involve relevant HCPs compliantly in new developments / data surrounding the product
Drive involvement of relevant HCPs at internal and external local, national and international meetings
Drive appropriate involvement of relevant HCPs with publications and product communications

People Responsibilities

Works closely with direct reports like Medical Affairs Professional (MAP) on performance management plans (objectives), development plans, and documentation of their expertise as and when there are direct reports to this position. Keeps these documents and plans up to date. Meets regularly with each direct report to coach, mentor, evaluate performance, evaluate training and development needs, and monitor career development goals. Maximizes each individual direct report s career potential, maximizing the value to the organization
Actively participate in recruitment, diversity, and retention efforts, and hiring efforts as applicable
Works closely with dotted line reports ie Medical Science Liaisons (MSLs) for enhancing their scientific knowledge on disease area and clinical trial data of the product, provide inputs for preparing field medical plans and its execution along with MSL Lead / Manager and MSLs. Participates in performance management discussions along with MSL Lead / Manager of the MSLs

Qualifications:

*Basic Requirements: Education and Experience

Basic Medical Qualification (MBBS/MD)
Full Medical Council registration or fulfilment of its eligibility criteria
Therapeutic area clinical and/or industry expertise within Neuroscience domain (highly desirable)
Evidence of strong teamwork and interpersonal skills
Demonstrated ability to balance scientific priorities with business priorities
Demonstration of initiative and motivation.
Demonstrated strong communication, interpersonal, teamwork, organizational and negotiation skills
Leadership capabilities to identify and develop new opportunities
Excellent communication skills (presentation, written and verbal)
Excellent self-management skills.
Demonstrated ability to plan, organise, prioritise and adapt to changing needs
Awareness of the role of medical doctors in a commercial setting
Ability to engage in domestic and international travel to the degree appropriate to support the business of the team.
Fluent in English, verbal and written communication.