Clinical Research Coordinator

About the Opportunity 

Our client is one of the leading medical centers in the Greater NYC Area and they are in need of a Clinical Research Coordinator to join their office in New York City. In this role, you will gain valuable experience in cancer research under the guidance of the Clinical Research Manager. This is an exciting opportunity to collaborate with dedicated physicians and other clinical team members, fostering a collaborative environment focused on providing exceptional patient care.

The annual base salary range is $60,000 to $72,500. Actual compensation offered to the successful candidate may vary from posted hiring range based upon geographic location, work experience, education, and/or skill level, among other things. Details about eligibility for bonus compensation (if applicable) will be finalized at the time of offer.

 

Job Responsibilities

  • Prepare IRB/Regulatory submissions, including initial submission, continuing reviews, and amendments. Maintain knowledge of IRB reporting requirements and communicate as needed within specified timeframes
  • Ensure protocol adherence and train clinical staff on protocol-specific tasks
  • Participate in tumor boards and other committees, as assigned
  • Facilitate, maintain, and coordinate all logistical aspects of clinical trials with all staff in accordance with Good Clinical Practice, sponsor, local, and federal regulations
  • Ensure accurate and complete submission of all study documentation, source documentation, and case report forms as required by study sponsors
  • Indicate to billing department which patient visits and procedures are study related or not
  • Serve as central contact between Principal Investigators, co-Investigators, study team, sponsors and study site participants regarding study procedures, patient concerns, serious safety events, and other protocol-related issues

 

Job Requirements

  • Minimum of a Bachelors degree in a related field (Psychology, Sociology, Biological Science, Statistics, Public Health, etc.)
  • Minimum of 1-3 years of relevant experience
  • Certified Clinical Research Coordinator/Professional (CCRC/CCRP) is preferred
  • Knowledgeable in Clinical Research protocols

Learn & Grow

Lorem ipsum dolor sit amet consectetur. Fames porta suspendisse ultrices ultricies

Gym

Lorem ipsum dolor sit amet consectetur. Fames porta suspendisse ultrices ultricies

Personal Days

Lorem ipsum dolor sit amet consectetur. Fames porta suspendisse ultrices ultricies

Health & Dental

Lorem ipsum dolor sit amet consectetur. Fames porta suspendisse ultrices ultricies

401k Matching

Lorem ipsum dolor sit amet consectetur. Fames porta suspendisse ultrices ultricies

Submit Your Resume

Connect with our staffing & recruiting experts! Let our team of expert recruiters help find your perfect match.

Max. file size: 12 GB.
This field is for validation purposes and should be left unchanged.

Other Positions

Field Reimbursement Manager

Location: Remote, USA
arrow

Director of Supply Chain

Location: Princeton, New Jersey (Hybrid)
arrow

Lead / Senior Data Manager

Location: Somerset, New Jersey
arrow

Sr. Principal / AD of Biostatistics

Location: Wilmington, Delaware
arrow

Study Start Up Specialist / Lead

Location: Remote, United States
arrow

Senior / Principal Biostatistician

Location: Little Falls, New Jersey (Remote)
arrow

Lead Clinical Data Manager

Location: Somerset, New Jersey (Remote)
arrow

Job Placement Resources

Boost your resume, interview skills to prepare for career advancement.