Clinical Scientist- FSP

Parexel International; United States; Remote; USD 110,000 - 140,000; Full time

Job summary

Parexel International is seeking a Clinical Scientist to support clinical trial operations, medical monitoring, and data reconciliation. You will assist in adjudication processes, prepare meeting materials, and liaise with stakeholders to drive study objectives.

The role requires strong communication, MS Office proficiency, and a willingness to travel for key company meetings. A life sciences degree with clinical development experience is preferred.

Qualifications

• High level communication skills, both written and verbal.
• MS Office Suite proficiency including Word, Excel, PowerPoint.
• Proficient in English; local language skills a plus where applicable.

Responsibilities

• Assist with clinical/scientific conduct of clinical studies, including medical monitoring and data reconciliation.
• Support adjudication and preparation of meeting materials.
• Interact with internal and external stakeholders to support study objectives.
• Ensure compliance with Parexel standards, ICH-GCPs, and training requirements.
• Travel as required for key company meetings.

Skills

Communication

MS Office

English

Travel

Education

Life Sciences degree

Alternative clinical dev exp

Job description

PXL is hiring a Clinical Scientist!

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
• Proficient in written and spoken English
• Proficient in local language (as applicable)
• Willingness to travel as required for key company meetings

Knowledge and Experience:

• Pharmaceutical experience beneficial but not required
• Therapeutic Area (TA) specific experience beneficial
• 2 years medical monitoring experience preferred

Education:

• Bachelors/Masters/PhD in Life Sciences with 2+ years relevant career experience
• If no degree in Life Sciences, must have significant experience in clinical development (>5 years)

#LI-REMOTE 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.