Clinical Scientist - FSP

Parexel International; United States; Remote; USD 90,000 - 135,000; Full time

Job summary

Parexel International is seeking a Clinical Scientist to support the clinical/scientific conduct of oncology studies, including medical monitoring, adjudication support, and preparation of meeting materials. You will work with the CS Protocol Lead and study team to ensure compliant trial execution.

Ideal candidates have oncology experience, 2+ years of medical monitoring, and strong written/spoken English. You will interact with cross-functional teams, manage protocol deviations, and contribute

Qualifications

• Bachelor/Master/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)
• 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

Responsibilities

• Assist the CS Protocol Lead and study team with clinical/scientific conduct of clinical studies (e.g., adjudication support, medical monitoring, imaging data reconciliation, preparation of meeting materials, protocol deviation management)
• Provide clinical trial operational delivery support; may lead a single study or multiple studies
• Liaise with cross-functional teams and interact with internal/external stakeholders to support study objectives
• Maintain compliance with Parexel standards, training, ICH-GCPs, and required processes
• Demonstrate strong oral and written communication skills; proficient in English; travel as required

Skills

Communication

MS Office

Excel advanced

English proficiency

Travel willingness

Education

Life Sciences degree (B.S./M.S./Ph.D.)

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.