Senior Clinical Scientist

Senior Clinical Scientist/ Clinical Scientist Associate Director / Clinical Scientist Director

Location:

Remote US - East Coast

Working Pattern:

Full-Time \| Permanent

We are supporting an innovative clinical stage biotech in their search for a seasoned Senior Clinical Scientist/ Clinical Scientist Associate Director / Clinical Scientist Director, reporting to the Chief Medical Officer. This is an exciting opportunity to join a growing clinical development team, playing a key role in the scientific review and interpretation of clinical trial data across cutting-edge programmes.

This role offers the opportunity to work within a highly collaborative, cross-functional environment, contributing to the delivery of high-quality clinical studies while supporting patient safety and data integrity throughout the clinical development process

Everything you need to know about this role

You will support the ongoing medical and scientific review of clinical trial data, helping to identify clinically meaningful trends, ensure data quality and contribute to key clinical development activities.

Working closely with Clinical Development, Clinical Operations, Biometrics, Medical, Pharmacovigilance and Regulatory teams, you'll play an important role in supporting informed decision-making throughout the lifecycle of clinical studies.

You'll be involved in:

• Reviewing clinical, safety and efficacy data to identify trends, discrepancies and clinically relevant findings
• Performing patient-level data review, including laboratory results, adverse events, concomitant medications and protocol deviations
• Supporting medical data review activities, data cleaning and query management
• Reviewing clinical listings, tables, figures, dashboards and patient narratives
• Collaborating with cross-functional teams to support interim analyses, safety reviews and database lock activities
• Contributing to protocol amendments, case report forms and other study documentation
• Supporting safety signal identification and medical interpretation of clinical trial data
• Maintaining awareness of therapeutic area developments and emerging clinical evidence
• Contributing to the delivery of high-quality clinical development programmes

Experience and qualities that make you a strong fit

• Degree in Life Sciences, Medicine, Pharmacy or a related discipline (MSc, PhD, PharmD or MD preferred)
• Experience reviewing clinical trial data within a biotechnology, pharmaceutical or CRO environment -

(5 years\+ essential

)

• Experience within haematological oncology

(essential)

ideally multiple myeloma

(preferred)

• Strong understanding of clinical trial conduct, GCP, protocol requirements and medical terminology
• Ability to interpret complex clinical datasets and identify medically relevant trends and safety signals
• Familiarity with EDC systems, clinical data review tools and data visualisation outputs
• Excellent analytical skills and exceptional attention to detail
• Strong written and verbal communication skills
• Comfortable working collaboratively across multidisciplinary teams
• Proactive, organised and able to manage multiple priorities effectively

What's on offer?

• Competitive salary and comprehensive benefits package and generous annual bonus
• Remote working with the need to attend the Boston office for important business meetings as required
• Opportunity to join an innovative and growing biotechnology organisation
• Work on cutting-edge oncology clinical development programmes in a collaborative, science-led team
• Exposure to cross-functional clinical development activities

Apply today for your experience to be considered.