Clinical Scientific Expert

Clinical Scientific Expert
Job Type: Temporary
Location: Dublin (hybrid working)

SRG are partnered with a leading Global Pharmaceutical Company who have an opportunity for a Clinical Scientific Expert to support the business on an initial 6 month contract. This is a full-time role based primarily in Dublin, although some hybrid working is available. This opportunity will provide a key support to the global team, working to ensure clinical trial data and regulatory reports are of highest quality throughout the life cycle of each program.

Main Responsibilities include:

Ensuring high quality clinical trial data review/insights and analysis as directed by the Integrated Clinical Trial Team
Performing high quality clinical data review and identify clinical data insights through patient level review and trends analysis, supporting Interim Analysis, Database and Post Lock activities and facilitate resolution of clinical data issues
Contributing to the development the Data Review/Quality Plan (DRP/DQP) and data review strategy
Contributing to and facilitating data review process improvements
Supporting pharmacovigilance activities (e.g., reviewing/contributing to aggregate reports/patient narratives, attendance of Safety Monitoring Meetings - if required
Developing subject matter expertise (disease area knowledge, clinical data review tools and/or processes)
Skills/experience required:

Advanced degree in life sciences/healthcare (or clinically relevant degree) is required - Master's, PharmD, MPharm, PhD, MBBS, BDS, MD (MD or PhD strongly preferred)

1 year experience in pharmaceutical industry/ clinical research organization ideally
Basic knowledge in planning, executing, reporting and publishing global clinical studies in a pharmaceutical company or contract research organization.
Work experience in clinical operations preferable
Strong interpersonal skills and ability to work under pressure
Good negotiation and conflict resolution skills
Fundamental knowledge of Good Clinical Practice, clinical trial design, statistics, regulatory processes, and clinical development process
Demonstrates strong Medical / scientific writing skills.
Demonstrates knowledge and application of statistical analysis methodology and can identify trends and analyze / interpret / report data effectively.
Fluent English (oral and written)

To Apply

If you are interested and want to find out more about this role, please click to apply or contact Theo Charles to discuss further.

Carbon60, Lorien & SRG - The Impellam Group STEM Portfolio are acting as an Employment Business in relation to this vacancy