Clinical Scientist- FSP

Parexel

• $100K — $120K *
US-AnywhereRemote in United States
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's, Master's, or PhD in Life Sciences; or over 5 years of clinical development experience
  • 2+ years of relevant career experience in clinical research
  • 2 years of medical monitoring experience preferred
  • Strong oral and written communication skills
  • Proficient in MS Office Suite (Word, Excel, PowerPoint)
  • Ability to communicate fluently in English and local language as applicable
  • Willingness to travel for key company meetings

Responsibilities

  • Support the clinical/scientific conduct of clinical studies
  • Lead studies with limited scope like Survival Follow-up
  • Liaise with cross-functional teams and stakeholders
  • Manage protocol deviations and provide adjudication support
  • Prepare meeting materials and reconcile imaging data
  • Ensure compliance with training and reporting requirements
  • Maintain an in-depth understanding of Parexel processes and ICH-GCP standards

Benefits

  • Access to professional development opportunities
  • Comprehensive training curriculum
  • Ability to work across diverse therapeutic areas
  • Possibility for engagement in a variety of clinical studies
  • Collaborative environment with cross-functional teams
Full 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)

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