Clinical Scientist- FSP

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 FSP is seeking a Clinical Scientist for a remote role in Latin America!

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)