Job Description

Clinical Research Scientist
Job Number: 21-09987
 
Be part of a company that delivers life-changing healthcare solutions. Eclaro is looking for a Clinical Research Scientist for our client in Summit, NJ.
 
Eclaro’s client is a leader in the Biopharmaceutical Industry, providing quality, innovative, and affordable mediscines 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!
 

Responsibilities:
  • Review of clinical data within eCRF system, patient profiles, etc. to issue queries and clean data from clinical perspective.
  • Conduct review of ongoing summary data including: safety, primary efficacy variables, and laboratory data.
  • Assist the Clinical Research Physician to interface with project team members including: Clinical Operations, Data Management, Statistics, Drug Safety, Regulatory and Project Management.
  • Prepare or assist with preparation of key documents e.g. Investigator Brochures, regulatory submission documents, internal or external presentations, etc.
  • Protocol preparation (writing, reviewing, amending and cross-functional facilitation as appropriate).
  • Clinical study report preparation
  • Review literature and prepare summary documents for inclusion in IB, protocols regulatory submission documents, etc.
  • Participate and/or Lead team meetings as required
 
Required Qualifications:
  • Must have experience working on clinical trials as a Clinical Research Scientist from a sponsor's perspective.
  • Must have at least two years of direct Hematology/Oncology experience in a Clinical Research and Development capacity
  • Must have experience performing data review in Hematology/Oncology indications (note, this position is different in scope from a CRA position or clinical operations)
  • Experience in performing review of clinical trial data in order to identify trends in safety or efficacy data.
  • Ability to function independently in data review to identify discrepancies in clinical trial data and to write queries from a medical perspective.
  • Familiarity with Medidata, RAVE, J-review or other clinical databases or other data review tools (patient profiles, listings) would demonstrate the candidate's familiarity with the scope of work.
  • Some experience in medical writing such as authoring or co-authoring documents such as protocol, clinical study report, investigators brochure, patient narrative
  • Ability to communicate medical or clinical information to a physician.
  • Ability to understand clinical trial publications; understanding of disease
  • Degree in life sciences
 
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:
Monica Galang    
monica.galang@eclaro.com
8549990734
 
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

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