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Senior Clinical Research Coordinator

2 months ago

New York, New York, United States Aquent Full time
About the Role

We are seeking a highly skilled Clinical Research Coordinator to join our team at Aquent. As a key member of our research team, you will be responsible for managing clinical research studies and ensuring compliance with regulatory requirements.

Key Responsibilities
  • Manage clinical research studies, including participant recruitment, informed consent, and data collection
  • Coordinate research participant visits and study-related procedures, including travel logistics and reminder communications
  • Function as the primary point of contact for research participants, providing updates on study progress and facilitating involvement of other study team members
  • Manage participant visit scheduling and technical troubleshooting, escalating issues to the appropriate individual(s)
  • Solicit and record information regarding safety events and prepare safety event documentation for review by the Principal Investigator
  • Ensure scientific integrity of data and record source data accurately, including patient visit data within the source, CTMS, electronic reporting systems, and timely query resolution
  • Provide accurate and timely data collection, documentation, entry, and reporting in both Sponsor and Walgreens databases
  • Support the regulatory staff in the maintenance of regulatory documents in accordance with Walgreens SOPs and applicable regulations
  • Communicate and collaborate specific study requirements to the research team, including internal and external parties, sponsor, monitors, PI, and study participants
  • Maintain regular contact with the Principal Investigator and team to review study details (e.g., progress, adverse events, enrollment)
  • Maintain study supplies and issue appropriate participant stipends
  • Conduct clinical research study visits/procedures per protocol requirements, including obtaining vital signs, height, weight, EKG's, spirometry, medical history, medications, adverse events, and labs, as well as administering questionnaires and diaries
  • Ensure timely response to queries and documentation of study-related issues
  • Monitor site compliance with subject safety reporting, escalate issues, and develop or contribute to the development of tools, processes, and training to enhance subject safety during the conduct of a clinical study
Requirements
  • Experience overseeing multiple clinical trials concurrently, while maintaining attention to detail
  • Experience prioritizing tasks and resources, meeting deadlines, and being adaptable to changing priorities
Preferred Qualifications & Interests

The target hiring compensation range for this role is the equivalent of $34.79 to $38.66 an hour. Compensation is based on several factors including, but not limited to education, relevant work experience, relevant certifications, and location.

Additional benefits offered may include; medical health insurance and dental insurance, life insurance, and eligibility to participate in 401k plan with company match.