Description
We are seeking a Clinical Scientist to join our Clinical Development team, contributing to the design, execution, analysis, and reporting of clinical studies. As a key member of the team, you will provide scientific and operational expertise to ensure successful study execution and generation of high-quality clinical data.
Responsibilities:
- Contribute to clinical development plans and study design
- Support protocol, amendment, and informed consent development
- Evaluate emerging scientific and competitive data
- Participate in feasibility and site selection activities
- Partner with Clinical Operations to oversee study conduct
- Monitor enrollment, protocol deviations, and study performance
- Participate in investigator meetings and site engagement activities
- Support issue identification and resolution
- Review safety, efficacy, biomarker, and PK/PD data
- Identify trends and data quality concerns
- Collaborate on database lock and analysis activities
- Support interpretation of study results
- Prepare and review CSRs, abstracts, and presentations
- Support advisory boards and scientific congress activities
- Contribute to Investigator’s Brochures and regulatory submissions
Basic Qualifications:
- Minimum of a PharmD, PhD, MD, or equivalent
- A minimum of 3 years of clinical research or drug development experience
Preferred Qualifications:
- Experience drafting or reviewing clinical study protocols, informed consent forms, and clinical study reports
- Experience providing medical monitoring or clinical safety oversight
- Demonstrated ability to work effectively in cross-functional teams and with external partners
- Strong understanding of GCP and global regulations
- Excellent communication and collaboration skills
We offer a competitive salary, an annual bonus based on company performance, healthcare and wellbeing programs, pension plan membership, and shares and savings programme.
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