Share This Page
Explore the Possibilities
and Advance with Us.
Coord,Clinical Research I
Job Number: 2018-30880
Category: Research
Location: Worcester, MA
Shift: Day
Exempt/Non-Exempt: Exempt
Business Unit: UMass Chan Medical School
Department: School - Cancer Research Office (CRO) - W402510
Job Type: Full-Time
Salary Grade: 41
Union Code: Non Union Position -W60- Non Unit Professional
Num. Openings: 1
Post Date: April 28, 2018

GENERAL SUMMARY OF POSITION:

Under the direction of the Principle Investigator or designee, the Clinical Research Coordinator is responsible for all aspects of collection and management of data for complex treatment, ancillary, and prevention protocols regulated by the FDA or DHHS, and sponsored by federal agencies, foundations, industrial sponsors or UMass Medical School in support of clinical trials.

 

 

MAJOR RESPONSIBILITIES:

  • Participate in the development of protocol specific tools, (e.g., treatment data and/or therapeutic checklists) to aid with data submission 
  • Extract and transcribe treatment data from hospital and clinical records required to complete study patient’s record and sponsor’s case report forms.  Monitors quality and timelines of data submissions
  • Monitor status of all studies in database and ensures that all patient data (on-study and follow-up) are submitted, and respond to data queries from sponsoring organization, in a timely manner
  • Track and maintain accurate data of studies, accrual, and patient status activity in database
  • Maintain effective working relationships with research nurses and investigators participating in the study 
  • Monitor strict adherence to protocols.  Assure that cases are being finalized and reviewed by appropriate clinician 
  • Review protocol requirements with physicians and research nurses.  Identify and resolve issues with protocol compliance.  Keep principal investigator and research nurse aware of any issues on compliance
  • Ensure that protocol document has current amendments. Inform staff and updates database
  • Provide data to study investigators as requested and submits data for analysis. Run quality control checks on data prior to transfer
  • Serves as a resource to physician and nurses to locate information for special reports and treatment decisions
  • Adheres to Good Clinical Practice (GCP) guidelines and all human subject protection practices
  • Participate in all office staff meetings.  Present current status of studies assigned
  • Participate in regularly held Protocol Review Committee meetings
  • Participate in the documenting work procedures specific to new studies
  • Perform other duties as required.

 

 

REQUIRED QUALIFICATIONS:

  • Bachelor’s degree in a scientific or health care field, or equivalent experience. 
  • 1-3 years experience in on-study data management and data collection in a research organization.
  • Ability to read and understand complex protocols. 
  • Excellent computer skills including: proficiency in word processing; proficiency in relational databases.
  • High degree or organizational and analytical ability to manage data collection and protocol adherence.
  • Excellent interpersonal and oral communication skills
  • Good writing skills with the ability to compose correspondence

                                                                                                                                               

SUPERVISION RECEIVED

Under the direction of the Principle Investigator or designee

 

SUPERVISION EXERCISED: 

None

 

ENVIRONMENTAL WORKING CONDITIONS:

Usual office environment, laboratory, medical, surgical, and off campus study sites

Regulatory/IRB submission experience strongly preffered 

Oncology experience preferred

Check Out Our Advancing Careers 
HR Blog

UMass Chan Medical School was among 23 companies that stood out as 2023 “DEI champions,” according to The Boston Globe.   


Named a U.S. News & World Report
“2023 BEST MEDICAL GRAD SCHOOL”
for Primary Care and Research