Clinical Scientist/Sr. Clinical Scientist - Oncology

Parexel; United States; On-site; USD 90,000 - 130,000; Full time

Job summary

Parexel is seeking a Clinical Scientist in the United States to support the clinical/scientific conduct of studies, including adjudication, medical monitoring, and materials preparation. The role involves collaborating with study sites and cross-functional teams to ensure alignment with project objectives.

The candidate should have 2+ years of medical monitoring experience, oncology background, and a life sciences degree. Travel will be required for key meetings and site visits.

Qualifications

• Strong oral and written communication skills.
• Proficient in MS Word, Excel, and PowerPoint.
• Advanced Excel skills (pivot tables, VLOOKUPs).
• Proficient in written and spoken English.

Responsibilities

• Clinical Trial Operational Delivery support for studies; liaises with cross-functional teams.
• Ensures compliance with Parexel standards, training, and processes including ICH-GCPs.
• Prepare meeting materials, adjudication support, and medical monitoring activities.

Skills

Oral and written communication

MS Office Suite

Advanced Excel

English proficiency

Willingness to travel

Education

Life sciences degree (Bachelor/Master/PhD)

Alternative life sciences with experience

Job description

When our values align, there's no limit to what we can achieve.

At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do.

Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference.

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.