Clinical Scientist- FSP

Parexel; Nashville (TN); Remote; USD 90,000 - 130,000; Full time

Job summary

Parexel is hiring a Clinical Scientist to support the clinical study conduct, medical monitoring, and data reconciliation activities across projects. The role involves collaboration with the Protocol Lead and study team to ensure adherence to ICH-GCPs and Parexel standards.

The ideal candidate has 2+ years of relevant experience and a Life Sciences degree, with strong communication skills and willingness to travel for key meetings and sites.

Qualifications

• Solid communication skills, both written and oral.
• Proficient with Word, Excel and PowerPoint.
• Fluent in written and spoken English.
• Willingness to travel for key meetings and study activities.

Responsibilities

• Support clinical study conduct, including medical monitoring and data reconciliation.
• Assist protocol adherence, adverse event review, and meeting material preparation.
• Coordinate with study sites and cross-functional teams to achieve study objectives.

Skills

Communication

MS Office

English proficiency

Travel willingness

Education

Bachelor/Master/PhD Life Sciences

Clinical development experience >5 years

Tools

MS Office

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.