Top 52 Clinical research Jobs in Worcester Ma

Clinical Research Coordinator - Open Rank
University of Massachusetts Medical School —Worcester, MA
- $40,000 - $80,000 a year
- Full-time
- Hospital
- HIPAA
- Mid-level
Clinical Research Assistant
University of Massachusetts Medical School —Worcester, MA
- $36,000 - $40,000 a year
- Full-time
- Microsoft Outlook
- Computer literacy
- Bachelor's degree
Clinical Research Coordinator II
University of Massachusetts Medical School —Worcester, MA
- $23.08 - $27.88 an hour
- HIPAA
- Mid-level
- Bachelor's degree
12d
Clinical Research Coordinator III
University of Massachusetts Medical School —Worcester, MA
- $58,000 - $70,000 a year
- Full-time
- Mid-level
- 3 years
- Analysis skills
Clinical Research Coord I
University of Massachusetts Medical School —Worcester, MA
- $19.23 - $23.08 an hour
- Part-time
- HIPAA
- Office
- Bachelor's degree
14d
Research Coordinator I
University of Massachusetts Medical School —Shrewsbury, MA
- $40,000 - $45,000 a year
- Full-time
- Microsoft Outlook
- Databases
- Analysis skills
Clinical Research Associate
Alira Health —Framingham, MA
- Full-time
- Bachelor of Science
- English
- Mid-level
Clinical Research Coordinator, Framingham Heart Study
Boston University —Framingham, MA
- Part-time
- Communication skills
- Entry level
13h
Research Nurse Coordinator - Open Rank
University of Massachusetts Medical School —Worcester, MA
- $70,000 - $97,000 a year
- Full-time
- Nursing
- RN License
- BLS Certification
Sr. Clinical Trial Associate (Hybrid - Acton, MA)
Insulet Corporation —Acton, MA
- $76,400 - $114,575 a year
- Full-time
- Hybrid work
- Office
- Databases
- Bachelor's degree
- Health insurance
- Dental insurance
Clinical Research Coordinator, Per Diem, Framingham Heart Study
Boston University —Framingham, MA
- Per diem
- Entry level
4d
Senior Clinical Research Coordinator - Milford
Dana-Farber Cancer Institute —Milford, MA
- $73,600 - $83,000 a year
- Full-time
- 3 years
- Bachelor's degree
- Travel
Clinical Research Coordinator II - Nurse
Iterative Health —Webster, MA
- Full-time
- Nursing
- RN License
- Mid-level
Post-Doctoral Fellow
Worcester Polytechnic Institute —Worcester, MA
- Full-time
- Analysis skills
- University
- Doctor of Philosophy
Senior Manager, Global Clinical Affairs Data (Hybrid - Acton, MA)
Insulet Corporation —Acton, MA
- $147,000 - $220,500 a year
- Full-time
- Hybrid work
- 6 years
- System design
- HIPAA
- Health insurance
- Dental insurance
Manager, Medical Information
Sequel Med Tech —Marlborough, MA
- $75,000 - $140,000 a year
- Extended hours
- Hybrid work
- Nursing
- Medicine
- 5 years
- Health savings account
- Paid holidays
Senior Regulatory Medical Writer, Client-embedded, FSP
Thermo Fisher Scientific —Framingham, MA
- $105,000 - $125,000 a year
- Full-time
- Microsoft Outlook
- Bachelor's degree
- Team management
- Commuter assistance
- Paid parental leave
Project Lead
Hamilton Storage Technologies —Franklin, MA
- $115,000 - $135,000 a year
- Full-time
- 5 years
- Bachelor's degree
- Experience equivalent to degree accepted
- Disability insurance
- Health insurance
Fellow, Finance - Hybrid Portfolio Management
Boston Scientific —Marlboro, MA
- $131,700 - $250,200 a year
- Hybrid work
- CPA
- 11+ years
- Office
Part-time NP or PA-C - Clinical Research - 20 hrs/wk - fixed schedule M-F 8:30-12:30
Framingham Heart Study —Framingham, MA
- $55 an hour
- Part-time
- Background check
- Spanish
- Certified Nurse Practitioner
- Health insurance
- Dental insurance
Quick Apply
14d

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Clinical Research Coordinator - Open Rank

University of Massachusetts Medical School -
Worcester, MA

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Job Details

Full-time
$40,000 - $80,000 a year

Qualifications

Project team coordination
Project reporting
Staff supervision
Laboratory inventory control
Regulatory documents
Team supervision
Project documentation
Data quality assurance
HIPAA
Mid-level
Scientific research papers
Research project design
Research industry grant writing
Data integrity and documentation
Schedule management
Bachelor's degree
Team training
Data quality monitoring
Quality control
Informed consent procedures implementation
Managing clinical research teams
Clinical data report preparation
Health information regulatory compliance
Data interpretation
Implementing research protocols
Patient recruitment
Managing projects
Clinical research inspection readiness
Literature search services
Research regulatory compliance

Full Job Description

Overview:

POSITION SUMMARY:

Under the direction of the Principal Investigator (PI) or designee, the Clinical Research Coordinator is responsible for independently performing delegated tasks and procedures involving human subject research. This work includes coordination of regulatory activities and aspects of collection and management of data for research protocols related to treatment, ancillary services, and prevention practices.

This is an open-rank posting (there are 4 levels of Clinical Research Coordinator) - candidates will be hired into the level commensurate with their experience.

Responsibilities:

ESSENTIAL FUNCTIONS:

Clinical Research Coordinator I:

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

Clinical Research Coordinator II

Duties noted above plus:

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

Clinical Research Coordinator III

Duties noted above plus:

Assist with recruiting, screening, selecting, maintaining and terminating study subjects for multiple protocols
Ensure accuracy and completion of all regulatory documentation, including local or central IRB and study data. Provide data/support to study Investigators, sponsors and/or external monitors/auditors
Direct the activities of research support staff. Assist with the training of staff
Develop preliminary designs for study related 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 Board (IRB) processes

Sr Clinical Research Coordinator

Duties noted above plus:

Responsible for internal review/monitoring of clinical data for quality assurance purposes. Reports findings
Responsible for the smooth operation of all assigned studies on a day-to-day basis, 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 related 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 summary 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. Keep principal investigator and manager aware of any issues regarding compliance
Accountable for quality assurance reviews of study data
Assist with financial /operational aspects of grant and contracts. Responsible for clinical research billing review within the required timeframe.
Contribute independently to grant preparation, assessment of protocol feasibility, manuscript writing, data presentations and Institutional Review Board (IRB) processes

Qualifications:

REQUIRED QUALIFICATIONS:

Clinical Research Coordinator I:

Bachelor’s degree in a scientific or health related field, or equivalent experience
0-1 year of related experience
Ability to travel off site locations

Clinical Research Coordinator II:

Requirements noted for CRC I plus:
1-3 years of related experience

Clinical Research Coordinator III:

Requirements noted for CRC I plus:
3-5 years of related experience

Sr Clinical Research Coordinator:

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

Apply Now

Refine Your Search

clinical research jobs in worcester ma

Clinical Research Coordinator - Open Rank

Clinical Research Assistant

Clinical Research Coordinator II

Clinical Research Coordinator III

Clinical Research Coord I

Research Coordinator I

Clinical Research Associate

Clinical Research Coordinator, Framingham Heart Study

Research Nurse Coordinator - Open Rank

Sr. Clinical Trial Associate (Hybrid - Acton, MA)

Clinical Research Coordinator, Per Diem, Framingham Heart Study

Senior Clinical Research Coordinator - Milford

Clinical Research Coordinator II - Nurse

Post-Doctoral Fellow

Senior Manager, Global Clinical Affairs Data (Hybrid - Acton, MA)

Manager, Medical Information

Senior Regulatory Medical Writer, Client-embedded, FSP

Project Lead

Fellow, Finance - Hybrid Portfolio Management

Part-time NP or PA-C - Clinical Research - 20 hrs/wk - fixed schedule M-F 8:30-12:30

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