Clinical Scientist - FSP

Parexel; Hartford (CT); Remote; USD 95,000 - 135,000; Full time

Job summary

Parexel is seeking a Clinical Scientist to support the clinical/scientific conduct of oncology-focused studies. The role involves medical monitoring, adjudication support, and preparing materials for meetings, with liaison across sites and committees.

Oncology experience is required, plus familiarity with ICH-GCPs and Parexel processes. Ideal candidates will have 2+ years of medical monitoring experience, strong Excel skills, and excellent English communication.

Qualifications

• Oncology experience preferred and required where stated.
• 2+ years medical monitoring experience preferred.
• Experience with adjudication support, imaging data reconciliation, and meeting materials preparation.
• Strong written and oral communication skills; fluent in English.

Responsibilities

• Assist the CS Protocol Lead and study team in the clinical/scientific conduct of studies.
• Coordinate with sites, committees, and stakeholders to meet study objectives.
• Ensure compliance with Parexel processes, ICH-GCPs and regulatory requirements.
• Prepare materials for investigator meetings and manage protocol deviations.

Skills

Oncology experience

Medical monitoring

Adjudication support

Imaging data reconciliation

Communication skills

MS Office (Excel pivot)

Willingness to travel

Education

Life Sciences degree (BSc/MSc/PhD)

Clinical development experience ≥5 years (if no Life Sciences degree)

Tools

MS Office

Excel (pivot tables, v-lookups)

PowerPoint

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.