Clinical Scientist- FSP

Parexel; Clayton (NC); In loco; USD 90.000 - 130.000; Tempo pieno

Descrizione del lavoro

Parexel in the United States seeks a Clinical Scientist to assist the protocol lead and study team with clinical/scientific conduct of trials, including medical monitoring and data reconciliation.

The role involves coordinating with cross-functional lines and external sites, ensuring adherence to Parexel processes, ICH-GCP, and regulatory requirements, with occasional travel for key company meetings.

Competenze

• Bachelor/Master/PhD in Life Sciences with 2+ years relevant career experience.
• If no Life Sciences degree, significant experience in clinical development (>5 years).
• 2 years medical monitoring experience preferred.

Mansioni

• Support clinical studies under Protocol Lead, including monitoring and data reconciliation.
• Ensure Parexel standards and ICH-GCP compliance.
• Coordinate with sites and study teams to meet objectives.

Conoscenze

Communication

MS Office

English Proficiency

Travel willingness

Formazione

Life Sciences degree (BSc/MSc/PhD)

Clinical development experience (>5 years) alternative

Descrizione del lavoro

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.

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)

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.