Clinical Scientist - FSP

Parexel; Little Rock (AR); Remote; USD 90,000 - 130,000; Full time

Job summary

Parexel is seeking a Clinical Scientist to support clinical study conduct, including medical monitoring, adjudication, and imaging data reconciliation. The role collaborates with the Protocol Lead and study teams to ensure protocol adherence and data integrity.

Experience in oncology is preferred; 2+ years in clinical development and strong English communication are required. Some travel to sites and meetings may be necessary.

Qualifications

• Oncology experience preferred
• 2+ years medical monitoring experience preferred
• Experience with adjudication, medical monitoring, imaging data reconciliation and protocol deviation management
• Pharmaceutical experience beneficial but not required

Responsibilities

• Clinical Trial Operational Delivery: may support a single study or multiple studies.
• Lead a study with limited scope when needed (e.g., Survival Follow-up).
• Liaises with cross-functional lines and stakeholders to support clinical study objectives.
• Complies with Parexel training, processes, and ICH-GCP requirements.
• Submits timesheets and expense reports; updates CV as required.

Skills

Communication

MS Office

Advanced Excel

English

Travel

Education

Bachelor/Master/PhD Life Sciences (2+ yrs exp)

Bachelor with >5 yrs clinical development (if no Life Sciences degree)

Tools

MS Office Suite

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.