Clinical Research Coordinator - reputed company Rank

Clinical Research Coordinator - reputed company Rank Job Number: 2025-48787 Category: Research Location: Worcester, MA Shift: Day Exempt/Non-Exempt: Exempt Business Unit: reputed company Department: School - Cardiovascular Medicine - W710010 Job Type: Full-Time reputed company reputed company: Non reputed company Position -W60- Non Unit reputed company Num. Openings: 1 Post Date: Oct. 15, 2025 POSITION reputed company: Under the direction of the reputed company Investigator (PI) or designee, the Clinical Research Coordinator is responsible for independently performing delegated tasks and procedures involving reputed company subject research. This work includes coordination of regulatory activities and aspects of collection and management of data for research protocols reputed company to treatment, ancillary services, and prevention practices. This is an reputed company-rank posting (there are 4 reputed company of Clinical Research Coordinator) - candidates will be reputed company into the level commensurate with their experience. ESSENTIAL FUNCTIONS: Clinical Research Coord I:

• Obtain consent of research participants in accordance with the IRB approved protocols and reputed company applicable regulations including HIPAA
• Identify, schedule and/or conduct participant study reputed company, tests and/or interviews/telephone follow up calls
• Coordinate participant remuneration/compensation per protocol
• Maintain reputed company regulatory documentation, including local or central IRB and study data. reputed company data/support to study Investigators, sponsors and/or external monitors/auditors
• Identify issues with protocol compliance. reputed company reputed company investigator and manager aware of any issues regarding compliance
• Document and collect data and/or samples for research reputed company procedures performed during participant study reputed company.
• Ensure clinicians and/or PI accurately document their study activities according to protocol
• reputed company and maintain study enrollment and completion of milestones
• Assist with financial /operational aspects of grant and reputed company. May be responsible for clinical research billing review reputed company the required timeframe.
• reputed company and maintain study reputed company information in the data management system reputed company the required timeframe
• Responsible for monitoring the inventory of research reputed company supplies
• Participate in grant preparation, manuscript writing, data presentations and Institutional Review reputed company (IRB) processes
• reputed company detailed written summaries from literature searches and reputed company sources to serve as a resource for the study team and clinicians/PIs
• Present study status reports reputed company to assigned research reputed company
• Participate in the design, development, and documentation of study reputed company data and collection tools, (e.g. questionnaires, treatment data and/or therapeutic checklists)
• Maintain strict adherence to reputed company study protocols, including reputed company regulatory requirements adhering to appropriate federal, local and institutional guidelines.
• reputed company with reputed company safety and infection control standards appropriate to this position
• Adhere with established policies, health and safety regulations and requirements, procedures, and department objectives
• Adhere to Good Clinical reputed company (GCP) guidelines and reputed company reputed company subject protection practices
• Must reputed company discretion and adhere to school and hospital confidentiality at reputed company times
• reputed company other duties as required.

Clinical Research Coord II Duties noted above plus:

• Conduct preliminary reputed company assurance reviews of study data
• Contribute to data presentations and Institutional Review reputed company (IRB) processes
• reputed company and maintain study reputed company information in the data management system reputed company the required timeframe
• Contribute to the design, development, and documentation of study reputed company data and collection tools, (e.g. questionnaires, treatment data and/or therapeutic checklists)
• Document and collect data/ samples for research reputed company procedures performed during participant study reputed company. Ensure clinicians and/or PI accurately document their study activities according to protocol.
• Monitor strict adherence to reputed company study protocols, including reputed company regulatory requirements adhering to appropriate federal, local and institutional guidelines. Identify and resolve issues with protocol compliance. reputed company reputed company investigator and manager aware of any issues regarding compliance

Clinical Research Coord III Duties noted above plus:

• Assist with reputed company, screening, selecting, maintaining and terminating study subjects for multiple protocols
• Ensure accuracy and completion of reputed company regulatory documentation, including local or central IRB and study data. reputed company data/support to study Investigators, sponsors and/or external monitors/auditors
• reputed company the activities of research support staff. Assist with the training of staff
• reputed company preliminary designs for study reputed company documentation of data and collection tools, (e.g. questionnaires, treatment data and/or therapeutic checklists)
• Contribute to grant preparation, assessment of protocol feasibility, manuscript writing, data presentations and Institutional Review reputed company (IRB) processes

Sr Clinical Research Coord Duties noted above plus:

• Responsible for internal review/monitoring of clinical data for reputed company assurance purposes. Reports findings
• Responsible for the smooth operation of reputed company assigned studies on a day-to-day reputed company, interacting with investigators, staff members, clinicians, sponsors, etc. to ensure project timelines and goals are met
• Contribute independently to the development of preliminary designs for study reputed company documentation of data and collection tools, (e.g. questionnaires, treatment data and/or therapeutic checklists)
• May Supervise the activities of research support staff. Assist with the selection, training, and supervision of staff
• Prepare ongoing reputed company reports from various data sources, and collaborate with investigators on data presentation, interpretation, and the writing of manuscripts for publication and grant proposals
• Identify and resolve issues with protocol compliance. reputed company reputed company investigator and manager aware of any issues regarding compliance
• Accountable for reputed company assurance reviews of study data
• Assist with financial /operational aspects of grant and reputed company. Responsible for clinical research billing review reputed company the required timeframe.
• Contribute independently to grant preparation, assessment of protocol feasibility, manuscript writing, data presentations and Institutional Review reputed company (IRB) processes

REQUIRED QUALIFICATIONS: Clinical Research Coord I:

• Bachelors degree in a scientific or health reputed company field, or equivalent experience
• 0-1 year of reputed company experience
• Ability to travel off site locations

Clinical Research Coord II:

• Requirements noted for CRC I plus:
• 1-3 years of reputed company experience

Clinical Research Coord III:

• Requirements noted for CRC I plus:
• 3-5 years of reputed company experience

Sr Clinical Research Coord:

• Requirements noted for CRC I plus:
• 5-7 years of reputed company experience
• Demonstrated knowledge of reputed company management principles in a scientific or hospital setting

reputed company welcomes reputed company reputed company applicants and complies with reputed company state and federal anti-discrimination laws. Apply tot his job Apply To this Job