Job Description

Clinical Scientist
Job Number: 21-10523
 
Be part of a company that delivers life-changing healthcare solutions. Eclaro is looking for a Clinical Scientist for our client in Summit, 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!
 
Responsibilities:
  • Will include, but are not limited to, the following:
    • Assist the Clinical Research Scientist team to interface with project team members including: Clinical Research Physician, Clinical Operations, Data Management, Statistics, Drug Safety, Regulatory and Project Management.
    • Review and query of hematology/oncology data including: safety, primary efficacy variables, and laboratory data.
    • Assist with protocol preparation (writing, reviewing, amending and cross-functional facilitation as appropriate).
    • Assist with Study Start up Activities and data base build
    • Participate or lead in Scientific meetings (i.e. Ad-Board, Steering Committee, Data Monitoring Committee)
    • Potentially assume study lead responsibilities, manage study, work independently
    • Multi-tasking, i.e. working on multiple studies and/or multiple deliverables
 
Required Skills:
  • Excellent written and verbal communication skills and interpersonal skills.
  • Knowledge of clinical trial design, basic statistics, and data review tools
  • Proficient at data interpretation
  • Experience in protocol development, study report preparation, Investigator Brochure preparation, regulatory submissions
  • Full understanding GCP and ICH Guidelines
  • Detail-oriented, well-organized
  • Ability to assimilate technical and scientific information quickly
  • Proficient in Microsoft Office (Word, Excel, PowerPoint; Microsoft project a plus), JReview, EDC (Rave)
  • Demonstrated ability to work as part of a team
  • Hematology experience (plus).
  • Protocol authoring (preferred).
  • Data review and medical monitoring of data (required).
 
Qualifications:
  • Minimum 6 yrs. experience in oncology/hematology clinical development
  • Advanced Degree in Life Sciences (e.g., nursing, pharmacy or related medical field), minimum 5 years' experience in clinical research development or equivalent
 
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:
Paul Quibuyen
Christian.Quibuyen@eclaro.com
646-695-2942
Paul Quibuyen | 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

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