Clinical Research Scientist - Medical Affairs

Clinical Research Scientist - Medical Affairs

Eli Lilly Benelux

Cork, Ireland

Responsibilities:

As a CRS, you will be an integral member of cross-functional teams, collaborating with other CRS and Clinical Research Physicians. Your responsibilities include:

• Developing global and/or regional clinical/medical plans;
• Contributing to the development of promotional materials and medical strategies;
• Supporting business-to-business and business-to-government activities;
• Engaging in scientific data dissemination and exchange;
• Participating in clinical planning, trial execution and reporting;
• Providing regulatory support activities.

You will work closely with internal teams such as Clinical Development, Global Scientific Communications, Global Medical Information, Global Patient Safety, Value, Evidence and Outcomes, and the International Business Unit.

Basic Requirements:

• An advanced health/medical/scientific (pharmacology, physiology, microbiology) or related graduate degree such as Doctor of Veterinary Medicine (DVM), Doctor of Pharmacy (PharmD), Doctor of Philosophy (PhD), Master of Science in Nursing (MSN) with advanced clinical specialty (Clinical Nurse Specialist/Nurse Practitioner) and one of following: 3-5 years of clinical experience; or 3-5 years of pharmaceutical experience (including 2 years in clinical development); OR
• Bachelor’s or Master’s degree in health/medical/scientific or related field with 7-10 years of pharmaceutical experience directly related to clinical trials, drug discovery, or drug/clinical development (e.g., epidemiology, toxicology, pharmacology, regulatory affairs, medical affairs);
• Strong communication, interpersonal, teamwork, organizational, and negotiation skills;
• Ability to balance scientific priorities with business priorities and influence others cross-functionally;
• Fluency in English, both verbal and written communication;
• Flexibility to engage in domestic and international travel as needed to support the business objectives.

Additional Skills/Preferences:

• Proficient in data analysis and interpretation;
• Prior work with cross-functional teams and ability to collaborate effectively across different departments;
• Proven ability to effectively communicate scientific and clinical information to diverse audiences;
• Familiarity with regulatory requirements and guidelines for clinical research and drug development;
• Experience in conducting literature reviews and staying abreast of developments in the field of Immunology;
• Demonstrated ability to adapt to changing priorities and work effectively in a fast-paced environment.

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