Job Description

Study Assessment Planning Associate

Job Number: 21-13616

 

Be part of a company that delivers life-changing healthcare solutions. Eclaro is looking for a Study Assessment Planning Associate for our client in Lawrenceville, NJ.

 

Eclaro’s client is a leader in the Biopharmaceutical Industry, providing quality, innovative, and affordable medicines that make a difference in the lives of patients all over the world. If you’re up to the challenge, then take a chance at this rewarding opportunity!

 

Required Qualifications:

  • Comprehensive understanding of clinical trial operations, including PK, PD, Laboratory Safety testing, and additional protocol assessments terminology.
  • Knowledge of clinical design trial
  • Understanding of Time and Event tables captured in clinical trial protocols
  • Ability to proactively identify issues, make decisions, and resolve problems
  • Demonstrates a strong understanding of the overall project goals and deadlines
  • Bachelor's Degree required - B.S. A degree in Life Sciences or equivalent is preferred.

 

Preferred Skills:

  • Knowledge of general clinical research including Investigator site processes, site operations
  • Knowledge of the pharmaceutical industry including the clinical and regulatory components.
  • Background in QC
  • Experience in robust data review
  • Experience in protocol authoring
  • Understanding of sample handling management, collection and testing tube experience, and shipping logistics
  • Management of clinical trial activities during study start up and execution
  • Reviews the clinical protocol to identify study design, planned Assessments, and details of time and event schedules
  • Provides assistance to ensure data quality and integrity for historical and on-going Client trials
  • Manages metadata required at a protocol level
  • Data review responsibilities for assessment and visit matrix alignment
  • Can manage working on multiple studies at any given time
  • Drives and owns timelines for assigned projects
  • Assists with development data quality for BMC clinical trial database
  • 3 + years of clinical trials in a pharma research or central clinical lab organization
  • Desirable attributes/skills: Project Management, Excel

 

If hired, you will enjoy the following Eclaro Benefits:

  • 401k Retirement Savings Plan administered by Merrill Lynch
  • Commuter Check Pretax Commuter Benefits
  • Eligibility to purchase Medical, Dental & Vision Insurance through Eclaro

 

If interested, you may contact:

Jane Bautista

froilyn.bautista@eclaro.com

2012858622

Jane Bautista | LinkedIn

 

Equal Opportunity Employer: Eclaro values diversity and does not discriminate based on Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.

Application Instructions

Please click on the link below to apply for this position. A new window will open and direct you to apply at our corporate careers page. We look forward to hearing from you!

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