Healthcare Clinical Scientific Expert I

What are we looking for in our Clinical Scientific Expert I?

Exciting Career Opportunity! - Clinical Scientific Expert I in Dublin 4 - 06 months contract - Hybrid role with 3 days onsite

Join one of the world's premier pharmaceutical companies making a significant impact on patients lives and the Irish economy.  We are looking for a Clinical Scientific Expert I (CSE I)  who provides clinical and scientific support through all phases of a clinical study under the guidance of the (A)CD(M)D in compliance with client processes, ICH GCP and regulatory requirement

Job Purpose:

The Clinical Scientific Expert I (CSE I) provides clinical and scientific support through all phases of a clinical study under the guidance of the (A)CD(M)D in compliance with client processes, ICH GCP and regulatory requirements. This role applies the principles of clinical data review excellence and identifies clinical data insights to ensure data is scientifically plausible and to identify trends, signals and risks associated to trial endpoints and patient safety. The CSE I is a core member of the Integrated Clinical Trial Team (iCTT) and may support program level activities as assigned.

Major Activities

Responsibility for ensuring high quality clinical trial data review/insights and analysis as directed by the Integrated Clinical Trial Team (iCTT):

1. Perform 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. Collaborate with relevant line functions to enhance the quality of clinical data review/insights with an emphasis on subject safety and eligibility, data integrity, trend identification, analysis and remediation, and identification of cases for medical review.
2. Contributes to the development the Data Review/Quality Plan (DRP/DQP) and data review strategy, ensuring that protocol-level deviations, eligibility criteria, study assessments & other aspects of the protocol are implemented consistently across the study.
3. In conjunction with the relevant line functions, may contribute to Case Report Form (CRF) development, and support the implementation of data capture tools.
4. Contribute to and facilitate data review process improvements e.g. identification of delinquent/redundant reports and/or implementation of innovative data analysis processes and tools.
5. May contribute (in collaboration with relevant line functions) to the development of study-level documents, including clinical sections of key regulatory documents, such as Investigator’s Brochures, briefing books, safety updates and submission dossiers. In collaboration with relevant line functions, review/write clinical trial documents for study CSR activities, and publications.
6. May support pharmacovigilance activities (e.g., reviewing/contributing to CSE I

aggregate reports/patient narratives, attendance of Safety Monitoring Meetings (SMT)), if required.

7. Produce training materials and provide training to iCTT.
8. Support/present at study level meetings (Investigator Meetings, Data Monitoring Committee (DMC) meetings or others), as required.

Other responsibilities include:

1. Develop subject matter expertise (disease area knowledge, clinical data review tools and/or processes).
2. Contribute to Clinical Development and Analytics (CD&A) line function initiatives, local and/or global education and process development projects, as required.

Key Performance Indicators (Indicate how performance for this job will be measured)

• Performing clinical data review and insights consistently and accurately which meets the Client quality standards, timelines, and is inspection ready.
• High quality contributions to study documents (e.g. protocol, ICF, clinical sections of CTA)
• Clearly demonstrates Client Values and Behaviors (i.e. Innovation, Quality, Collaboration, Performance, Courage and Integrity.

Impact on the organization: High quality data from scientifically sound trials

supporting strategic decision making and high quality health authority submissions.

Client seen as a credible, ethical and preferred partner by key investigators in the assigned therapy area.

Ideal Background (Pharma)

Education:

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

Languages:
Fluent English (oral and written)

What’s Offered:

• 6-month contract with potential for extension.
• Pay rate upto €20/hour (depending on experience).
• Hybrid work model (3 days per week in Dublin 4 office).
• Opportunity to work with a leading global pharmaceutical company dedicated to improving patients' futures.