Clinical Research Scientist, GPS Medical
Eli Lilly
- Indianapolis, IN
- Permanent
- Full-time
- Effectively function as part of multifunctional teams (e.g., safety managers, surveillance scientists, project managers, physicians from clinical teams or affiliates, statisticians, epidemiologists, writers, data management)
- Effectively interface with the global GPS organization, including safety groups in Affiliates and Regional Centers
- Core responsibilities will include, but are not limited to:
- Understanding the roles and responsibilities of the European Union Qualified Person for Pharmacovigilance (QPPV).
- Ensure support is provided to enable the QPPV to fulfill all the QPPV legal responsibilities
- Provide training, coaching and mentorship to safety surveillance scientists, and other Global Patient Safety Medical physicians and clinical research scientists.
- Maintain compliance with Lilly Red Book and corporate policies, Lilly Research Laboratories and Global Patient Safety curriculum map.
- Maintain compliance with the Lilly Corporate Integrity Agreement.
- Provide input to Global Patient Safety Medical Leadership Team and Safety Review Committee as required.
- Provide ad-hoc involvement in operations, if required.
- Act as the Lilly GPS Medical Representative for both internal and external customers, interacting as prescribed in corporate guidelines and policies.
- Build strong relationships with key customers, representing and championing the role of safety in the organization:
- For each level on every global path, there are a consistent set of job
- Advanced medical related graduate degree, such as: DVM, PharmD, PhD, MSN with advanced clinical specialty (Clinical Nurse Specialist/Nurse Practitioner) with 1-3 years’ experience in related scientific field, e.g. pharmacology, physiology, microbiology or scientifically related field.
- BS degree in health-related or scientific field with 7-10 years of experience in pharmaceutical industry, directly related clinical trial experience or experience in areas relevant to drug discovery or development, e.g. epidemiology, toxicology, pharmacovigilance, regulatory affairs.
- 3-5 years of clinical experience, or 2-5 years of pharmaceutical experience, at least 2 years of which was clinical development experience.
- Fluent in English; both written and verbal communications.
- Strong clinical/diagnostic skills.
- Strategic thinking.
- Demonstrated success in implementing projects.
- Good communication skills, both verbal and written.
- Team player.
- Ability to effectively function in a matrix environment.
- Interpersonal, organizational and negotiation skills.
- Ability to influence others (both cross-functionally and within the function) in order to create a positive working environment.
- Excellent teamwork skills.
- Willing to engage in domestic and international travel to the degree appropriate to support the business of the team.