Clinical Research Scientist – Medical Affairs

Job title:

Clinical Research Scientist – Medical Affairs

Company:

Eli Lilly

Job description

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.Eli Lilly Cork, is made up of a talented diverse team of over 2,000 employees across 38 nationalities who deliver innovative solutions that add value across a variety of Business Service functions including Finance, Information Technology, Medical, Clinical Trials and more.Lilly offers a premium workspace across our campus in Little Island, complete with flexible hybrid working options, healthcare, pension and life assurance benefits, subsidised canteen, onsite gym, travel subsidies and on-site parking. Inhouse People Development services, Educational Assistance, and our ‘Live Your BEST Life’ wellbeing initiatives are just some of the holistic benefits that enhance the career experience for our colleagues.Immunology Medical Affairs Clinical Research ScientistOrganization Overview:Eli Lilly GBS Cork, Ireland, hosts a unique ‘Global Medical Affairs’ role within the ‘Medical and Scientific Capabilities’ organization. This role supports the life cycle of the Immunology portfolio, contributing to strategic planning and collaboration with global teams in product development activities.Through the application of scientific and clinical expertise, the Clinical Research Scientist (CRS) is an integral member of the Medical Affairs team for strategic planning and execution.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.

Additional Information:

• Travel may be required, both domestically and internationally and is planned to be around 10-15% of the time.
• This position is based at Eli Lilly GBS Cork, Ireland.
• This position is a fixed term position for 12-month period.

Lilly is dedicated to helping individuals with disabilities to actively engage in the workforce, ensuring equal opportunities when vying for positions. If you require accommodation to submit a resume for a position at Lilly, please complete the accommodation request form ( ) for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.Lilly does not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity, gender expression, national origin, protected veteran status, disability or any other legally protected status.#WeAreLilly

Expected salary

Location

Cork

Job date

Sat, 17 May 2025 22:11:25 GMT

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