Clinical Scientist- FSP

Parexel; Providence (RI); On-site; USD 90,000 - 130,000; Full time

Job summary

Parexel is seeking a Clinical Scientist to assist the clinical and scientific conduct of studies, including adjudication support, medical monitoring, and preparation of meeting materials.

You will collaborate with the study team, liaise with sites and committees, and uphold Parexel processes, ICH-GCPs, and regulatory requirements. Strong communication and English proficiency are essential; travel to key meetings may be required.

Qualifications

• Bachelor/Master/PhD in Life Sciences with 2+ years relevant career experience.
• If no degree in Life Sciences, must have significant experience in clinical development (>5 years).
• MS Office Suite (Word, Excel, PowerPoint) and strong communication skills are required.

Responsibilities

• Support clinical studies under guidance of the Protocol Lead and study team.
• Provide medical monitoring and adjudication support as needed.
• Maintain compliance with Parexel standards, ICH-GCPs and internal processes.
• Coordinate with sites and committees and prepare meeting materials.

Skills

Oral & written communication

MS Office (Word, Excel, PowerPoint)

English proficiency

Local language proficiency

Travel willingness

Education

Life sciences degree (BSc/MSc/PhD)

Clinical development experience (>5 years) if no life sciences degree

Job description

PXL is hiring a Clinical Scientist!

Job Purpose:

The Clinical Scientist (CS) assists the CS Protocol Lead and study team with the clinical/scientific conduct of clinical studies (e.g., adjudication support, medical monitoring, imaging data reconciliation preparation of meeting materials, protocol deviation management).

Key Accountabilities

May include but not limited to the following:

Clinical Trial Operational Delivery

• May support a single study or multiple studies
• May lead a study with limited scope (e.g., Survival Follow-up)
• Liaises with cross-functional lines as appropriate
• May interact with internal and external stakeholders (study sites, committees, etc.) in support of clinical study objectives

Compliance with Parexel Standards

• Complies with required training curriculum
• Completes timesheets accurately as required
• Submits expense reports as required
• Updates CV as required
• Maintains a working knowledge of and complies with Parexel processes, ICH-GCPs and other applicable requirements

Skills:

• Demonstrated oral and written communication skills
• MS Office Suite Experience Required– including Word, Excel, and Power Point
• Proficient in written and spoken English
• Proficient in local language (as applicable)
• Willingness to travel as required for key company meetings

Knowledge and Experience:

• Pharmaceutical experience beneficial but not required
• Therapeutic Area (TA) specific experience beneficial
• 2 years medical monitoring experience preferred

Education:

• Bachelors/Masters/PhD in Life Sciences with 2+ years relevant career experience
• If no degree in Life Sciences, must have significant experience in clinical development (>5 years)

#LI-REMOTE

EEO Disclaimer

Parexel is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to legally protected status, which in the US includes race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or protected veteran status.