Job Description

Clinical Research Physician
Job Number: 21-08256
 
Be part of a company that delivers life-changing healthcare solutions. Eclaro is looking for a Clinical Research Physician for our client in Lawrence Township, 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!
 
Position Overview:
 
  • Serves as a primary source of medical accountability and oversight for clinical trials
  • Matrix management responsibilities across the internal and external network
  • Manages Phase 1 Phase 3 studies, with demonstrated decision making capabilities
  • Provides medical and scientific expertise to cross-functional Client colleagues
 
Responsibilities:
 
  • Medical Monitoring
    • Conducts medical data review of trial data, including eligibility review
    • Holds responsibility for site interactions in partnership with the Clinical Scientist (CS) for medical questions and education (including safety management guidelines)
    • Holds responsibility for assessment of key safety-related serious adverse events in partnership with Worldwide Patient Safety and oversees safety narratives
    • Collaborates with CS and inputs into protocols, providing medical strategic oversight in protocol development (input on inclusion/exclusion and other safety-related clinical considerations)
    • Fulfills GCP and compliance obligations for clinical conduct and maintains all required training
 
  • Clinical Development Expertise & Strategy
    • Provides oversight and medical accountability for a group of studies. Participates in review of clinical study reports (CSRs)
    • Leads the analysis of benefit/risk for clinical development protocols in a matrix team environment working with Clinical Scientists
    • Partners with CS to support executional delivery of studies (e.g., site activation, enrollment status, as well as adjudication for protocol violations, significant, non-significant deviations etc.)
    • Identifies and builds relationships with principal investigators. Identifies and cultivates thought leaders in order to gain their inputs on emerging science in drug and biomarker research, disease knowledge, and design of clinical development studies and programs
    • Maintains a strong medical/scientific reputation within the disease area. Has in-depth knowledge of etiology, natural history, diagnosis, and treatment of the disorder. Keeps up-to-date in the disease area by attending scientific conferences and ongoing review of the literature
    • Keeps abreast of development and regulatory issues related to other competitive or relevant compounds in development and how our portfolio fits into the competitive landscape
    • Provides ongoing medical education in partnership with CS to allow for protocol-specific training, supporting the study team, investigators, and others

Qualifications:
 
  • MD required
  • 3 or more years of Industry experience and/or clinical trials experience is required
 
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

6466952942
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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