Clinical Scientist - FSP

Parexel; Columbus (OH); Remote; USD 90,000 - 120,000; Full time

Job summary

Parexel is seeking a Clinical Scientist with oncology experience to assist in the clinical/scientific conduct of studies. You will support medical monitoring, imaging data reconciliation, and preparation of meeting materials, while managing protocol deviations and liaising with cross-functional teams.

The role involves interaction with study sites and committees, travel as required, and adherence to Parexel standards and ICH-GCP guidelines.

Qualifications

• 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.
• Bachelor/Master/PhD in Life Sciences or equivalent clinical development experience.

Responsibilities

• Assist the CS Protocol Lead and study team with clinical/scientific conduct of studies.
• Support medical monitoring, imaging data reconciliation, and preparation of meeting materials.
• Manage protocol deviations and liaise with cross-functional lines.
• Interact with study sites and committees to support clinical study objectives.

Skills

Oral communication

Written communication

MS Office

Advanced Excel

English proficiency

Willingness to travel

Education

Life sciences degree (Bachelor/Master/PhD)

Bachelor's degree with significant clinical development experience (>5 years)

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.