Clinical Scientist- FSP

Parexel; London; Remote; GBP 40,000 - 60,000; Full time

Job summary

A leading global clinical research organization is seeking a Clinical Scientist for a remote position to support clinical studies. Responsibilities include leading studies, engaging with stakeholders, and ensuring compliance with standards. A Bachelor's or higher in Life Sciences is required along with strong communication skills. The ideal candidate will have at least 2 years of relevant experience in clinical development.

Qualifications

• 2+ years of relevant experience in a related field.
• Pharmaceutical experience beneficial but not mandatory.
• Medical monitoring experience preferred.

Responsibilities

• Support one or multiple studies as a Clinical Scientist.
• Lead studies with limited scope and coordinate with teams.
• Engage with stakeholders to support study objectives.

Skills

Strong oral and written communication skills

Proficiency in MS Office Suite (Word, Excel, PowerPoint)

Fluent in English

Willingness to travel

Education

Bachelor’s, Master’s, or PhD in Life Sciences

Job description

When our values align, there's no limit to what we can achieve.

At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by a deep conviction in what we do.

Each of us, regardless of role, contributes to developing therapies that benefit patients. We take our work personally, act with empathy, and are committed to making a difference.

Parexel FSP is seeking a Clinical Scientist for a remote role in the EMEA.

Job Purpose:

The Clinical Scientist (CS) supports the CS Protocol Lead and study team in the clinical/scientific conduct of studies, including adjudication support, medical monitoring, imaging data reconciliation, meeting material preparation, and protocol deviation management.

Key Accountabilities:

• Clinical Trial Operational Delivery:
• Support one or multiple studies
• Lead studies with limited scope (e.g., Survival Follow-up)
• Coordinate with cross-functional teams as appropriate
• Engage with internal and external stakeholders (study sites, committees, etc.) to support study objectives

• Compliance with Parexel Standards:
• Complete required training and maintain updated CV
• Accurately submit timesheets and expense reports
• Maintain knowledge of Parexel processes, ICH-GCPs, and other applicable standards

Skills:

• Strong oral and written communication skills
• Proficiency in MS Office Suite (Word, Excel, PowerPoint)
• Fluent in English; proficiency in local language as applicable
• Willingness to travel as needed

Knowledge and Experience:

• Pharmaceutical experience beneficial but not mandatory
• Therapeutic Area experience advantageous
• At least 2 years of medical monitoring experience preferred

Education:

• Bachelor’s, Master’s, or PhD in Life Sciences with 2+ years of relevant experience
• If no Life Sciences degree, significant clinical development experience (>5 years)