Clinical Scientist - FSP

Parexel; Richmond (VA); Remote; USD 90,000 - 140,000; Full time

Job summary

Parexel is seeking a Clinical Scientist to assist in the clinical/scientific conduct of clinical studies, including medical monitoring, adjudication support, and imaging data reconciliation. You will support the Protocol Lead, interact with cross-functional teams and study sites, and help prepare meeting materials while ensuring compliance with ICH-GCP and Parexel standards.

Oncology experience is required and 2+ years of medical monitoring experience are preferred, with willingness to travel

Qualifications

• Oncology experience is required.
• 2+ years of medical monitoring experience preferred.
• Experience with adjudication support, medical monitoring, imaging data reconciliation, and protocol deviation management.
• Strong communication and cross-functional collaboration skills.

Responsibilities

• Support the clinical studies under supervision of the CS Protocol Lead.
• Provide medical monitoring and adjudication support for studies.
• Prepare meeting materials and manage protocol deviations as needed.
• Liaise with study sites and internal stakeholders to meet objectives.
• Ensure compliance with Parexel processes, ICH-GCPs and applicable requirements.

Skills

Oral and written communication

Advanced Excel

English proficiency

Willingness to travel

Education

Bachelor's/Master's/PhD in Life Sciences

Alternative: Bachelor's with >5 years clinical development experience

Tools

MS Office Suite

Excel (pivot tables & v-lookups)

Job description

Oncology experience preferred

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
• Advanced Excel skills required (pivot tables, v-lookups)
• Proficient in written and spoken English
• Willingness to travel as required for key company meetings

Knowledge and Experience

• Pharmaceutical experience beneficial but not required
• Oncology experience is required
• 2 years medical monitoring experience preferred
• Experience with adjudication support, medical monitoring, imaging data reconciliation preparation of meeting materials, and protocol deviation management

Education

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

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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.