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Senior Clinical Research Coordinator

Iterative Scopes
Cambridge, MA
  • Expired: over a month ago. Applications are no longer accepted.
Job Description
Iterative Scopes is hiring a Senior Clinical Research Coordinator to join our team of clinical research staff, specializing in augmenting research capabilities at sites participating in studies we service.
This position is a travel position that will entail 2-3 month assignments at research centers located across the United States
The right candidate for this position is:
  • Interested in supporting research activities for gastrointestinal studies, such as clinical trials for Inflammatory Bowel Disease
  • Enjoys learning and working as part of a team
Job Overview: 
The Senior Clinical Research Coordinator (CRC) is a specialized research professional working with and under the direction of the Site Manager and Principal Investigator (PI), but reporting into the Clinical Operations team at Iterative Scopes. The CRC is responsible for overseeing the day-to-day operations of clinical trials and studies. The CRC supports, facilitates, and coordinates the daily clinical trial activities and plays a critical role in the conduct of the study.

Key Responsibilities
  • Oversee the trouble-free running of clinical trials
  • Responsible for ensuring study compliance with local and federal laws and regulations
  • Recruiting and screening potential study participants and performing intake assessments
  • Attends meetings, events, and seminars to promote studies
  • Collecting data obtained from research, coding and analyzing it
  • Maintaining research records of study activity, including case report forms, drug dispensation records, or other regulatory forms per FDA guidelines
  • Communicating with participants regarding study objectives
  • Administering questionnaires and monitoring participants to ensure they adhere to the study’s rules and guidelines
  • Monitoring the study to ensure that it complies with protocols, is ethically conducted, and follows regulatory standards
  • Directing the collection, labeling, storage, and transport of all specimens
  • Managing budgets set aside for research
  • Making sure that all equipment and supplies needed for the study are in stock and in good working order
  • Protects the rights and welfare of all human research participants involved in research.
  • Other duties as assigned.

Requirements & Qualifications
Ideal Candidate Profile:
  • 3+ years of experience as a Clinical Research Coordinator working on IBD clinical trials, or clinical trials more generally in GI
  • Be willing to relocate/travel as needed to sites within a given notice period
  • Able to work effectively and communicate while at different (site) locations.
  • Excellent written and verbal communication skills
  • Knowledge of grammar, spelling, and punctuation.
  • Knowledge of purchasing, budgeting, and inventory control.
  • Capable of working independently with minimal supervision and as part of a team.
  • Skilled with standard computer programs including the Microsoft Office suite
  • Superior organizational and time management skills
  • Excellent communication, organizational, and collaboration skills 
  • Ability to work under pressure, communicate and present information.
  • Ability to read, interpret, and apply clinic policies and procedures.
  • Strong decision-making and prioritization skills
  • Ability to multi-task, establish priorities, and coordinate work activities.
Minimum Qualifications:
  • Minimum of 2 years experience as a Clinical Research Coordinator
  • Fast learner and a team player
  • Ability to complete tasks and deal with ambiguity
  • Experience working with cross-functional stakeholders in a business environment
  • Willingness and capability to travel  
Preferred Qualifications:
  • Proven track record as a CRC with the proven ability to recruit and randomize patients in the clinical trial setting
  • Confidence and experience presenting to all audiences

  • Medical, Dental, Vision, and Disability
  • Maternity/Paternity leave
  • Flexible time off
  • Wellness perks
  • IT / Workspace benefits
  • Commuter benefits, including subsidized parking
  • 401K
  • Stock Options

Iterative Scopes


Cambridge, MA



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