Top 196 Clinical research coordinator Jobs in Abington, Ma

Clinical Research Coordinator II - Foxborough
Dana-Farber Cancer Institute —Foxborough, MA
- $56,000 - $62,700 a year
- Full-time
- Mid-level
- Databases
- Bachelor's degree
Clinical Records Coordinator
Autumn Hospice —Norwell, MA
- Full-time
- HIPAA
- Mid-level
- High school diploma or GED
- Health insurance
- 401(k)
Quick Apply
Clinical Research Coordinator - Population Sciences
Dana-Farber Cancer Institute —Boston, MA
- $48,100 - $54,400 a year
- Full-time
- Office
- Bachelor's degree
- Data entry
Clinical Research Coordinator - MEE
Massachusetts Eye and Ear Infirmary —Boston, MA
- $29.01 an hour
- Part-time
- Hospital
- Computer literacy
- Bachelor's degree
- Opportunities for advancement
Quick Apply
4d
Clinical Research Coordinator I/II/III Opportunities – Multiple Locations Nationwide
Headlands Research —Boston, MA
- $45,000 - $100,000 a year
- Bachelor's degree
- Psychology
- Communication skills
Quick Apply
Clinical Research Coordinator
The Vascular Care Group —Wellesley, MA
- Hybrid work
- Patient monitoring
- Clinic experience
- Mid-level
Quick Apply
Clinical Research Coordinator I
The General Hospital Corporation —Boston, MA
- $21.00 - $29.01 an hour
- Full-time
- Hospital
- Computer literacy
- Bachelor's degree
- Opportunities for advancement
Quick Apply
9d
Clinical Research Coordinator - Neurosurgery Research
Boston Children's Hospital —Boston, MA
- $52,228.80 - $83,564.00 a year
- Full-time
- Mid-level
- Office
- Bachelor's degree
9d
Sports Concussion Clinical Research Coordinator II
The Spaulding Rehabilitation Hospital Corporation —Boston, MA
- $39.43 an hour
- Full-time
- Hybrid work
- Hospital
- Mid-level
- Bachelor's degree
- Opportunities for advancement
Quick Apply
1d
Clinical Research Associate II
AbbVie —Boston, MA
- $84,500 - $162,000 a year
- Full-time
- Remote
- Nursing
- Mid-level
- Organizational skills
- Paid holidays
- Health insurance
Clinical Research Coordinator
Alcanza Clinical Research —Roslindale, MA
- Full-time
- Spanish
- LVN
- HIPAA
- Health savings account
- Disability insurance
Quick Apply
1d
Clinical Research Assistant
Adams Clinical —Boston, MA
- $24.00 - $26.92 an hour
- Vital signs
- High school diploma or GED
- Bachelor's degree
- Health savings account
- Health insurance
Clinical Research Coordinator I - Urology
The Brigham and Women's Hospital, Inc. —Boston, MA
- $21.00 - $29.01 an hour
- Full-time
- Hybrid work
- Bachelor's degree
- Human resources
- Mentoring
- Opportunities for advancement
Quick Apply
Clinical Research Coordinator - Brighton
Dana-Farber Cancer Institute —Brighton, MA
- $48,100 - $54,400 a year
- Full-time
- Mid-level
- Databases
- Bachelor's degree
Clinical Research Coordinator - Thoracic Oncology
Dana-Farber Cancer Institute —Brookline, MA
- $48,100 - $54,400 a year
- Full-time
- Mid-level
- Bachelor's degree
- Travel
Clinical Administrative Coordinator
UnitedHealthcare —Boston, MA
- $18 - $32 an hour
- 8 hour shift
- Remote
- Microsoft Outlook
- Pass drug screening
- Mid-level
- AD&D insurance
- Employee stock purchase plan
2d
Clinical Research Coordinator II - Attleboro
Dana-Farber Cancer Institute —Attleboro, MA
- $56,000 - $62,700 a year
- Full-time
- Computer literacy
- Mid-level
- Bachelor's degree
Clinical Research Associate
Alira Health —Boston, MA
- $85,000 - $125,000 a year
- Full-time
- Bachelor of Science
- English
- Mid-level
Clinical Research Coordinator I
The Brigham and Women's Hospital, Inc. —Boston, MA
- $21.00 - $29.01 an hour
- Full-time
- Surgery
- Computer literacy
- Adults
- Opportunities for advancement
Quick Apply
2d
Clinical Research Coordinator
New England College of Optometry —Boston, MA
- $60,000 a year
- Full-time
- 5 years
- Mid-level
- University
- Paid holidays
- Disability insurance
Quick Apply

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Clinical Research Coordinator II - Foxborough

Dana-Farber Cancer Institute -
Foxborough, MA

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Job Details

Full-time
$56,000 - $62,700 a year

Qualifications

Bachelor's degree
Productivity software
Clinical confidentiality policies

Full Job Description

Job Ref:

JR-3671

Location:

22 Patriot Place, FOXBOROUGH, MA 02035

Category:

Clinical Research

Employment Type:

Full time

Work Location:

Onsite: occasional remote

Salary/Pay Rate:

$56,000.00 - $62,700.00 per year

Overview

The Clinical Research Coordinator II (CRC II) will work within the Dana-Farber Foxborough Satellite clinical research program and support the research team in the overall conduct of clinical trials using Good Clinical Practice under the auspices of the Principal Investigator(s) and the DFCI disease programs. The Satellite CRC will be responsible for the primary data collection, management of patient clinical information, and regulatory documents as it pertains to participation in clinical trials across all studies open at the Satellite site(s). Ensures timely collection of protocol related samples including shipment to outside entities as required. Maintains site regulatory binders and ensures study compliance with all state, federal, and IRB requirements. May be responsible for site IRB submissions (violations, deviations, severe adverse event reports). This individual may also screen patients for protocol eligibility, obtain informed consent (minimal risk studies), and register study participants to clinical trials. Travel to the Longwood campus and other DFCI Satellite sites may be required.

Located in Boston and the surrounding communities, Dana-Farber Cancer Institute is a leader in life changing breakthroughs in cancer research and patient care. We are united in our mission of conquering cancer, HIV/AIDS, and related diseases. We strive to create an inclusive, diverse, and equitable environment where we provide compassionate and comprehensive care to patients of all backgrounds, and design programs to promote public health particularly among high-risk and underserved populations. We conduct groundbreaking research that advances treatment, we educate tomorrow's physician/researchers, and we work with amazing partners, including other Harvard Medical School-affiliated hospitals.

Oversight of the clinical trials regulatory process at the DFCI Satellite(s) and site activation activities
Communication and coordination with the lead study team at the Longwood campus for study start-up, ongoing study team meetings, and project management of all site study activities
Responsible for data reporting and management, collection of source documents, use of case report forms, adverse events reporting, filing and archiving of study records, and resolution of data queries for all studies at the Satellite site(s)
Prepare and/or complete regulatory related reports and IRB submissions as it pertains to the satellite’s studies. Maintain and organize study regulatory binders, enter all required study data on an ongoing basis
Maintains various regulatory tracking databases with information related to study recruitment, subject enrollment, and study progress and completion
Ensure all study related samples are collected, properly prepared and shipped according to the protocol requirements and IATA/DOT regulations
Responsible for organizing and preparing for both internal and external auditing and study monitoring visits
Coordination and management of all clinical trials at the Satellite site(s), including communication with Sponsors and regulatory authorities
Close-out of clinical trials, including contributing to research articles, audit preparation, and communication with regulatory agencies and other disciplines involved
Interact with study participants as directed/required by the protocol and/or study team
May be responsible for tissue sample work
Travel between DFCI satellite locations to support all above research activities when cross coverage is needed
Maintain working knowledge of current regulations, regulatory guidance and or local policies
May be responsible for preparing and presenting study status regulatory status for satellite site clinical team members at monthly research meetings

COMPETENCIES:

Demonstrates understanding of CRF completion, including timely and accurate transcription of study data
Shows an understanding in coordinating and managing clinical research studies
Shows an understanding of ICH/GCP and Federal Regulatory requirements
Shows an understanding of DF/HCC SOPs
Shows an understanding of the roles and responsibilities of other key departments within clinical research (ex. OHRS, ODQ, DFCI CTO etc.)
Proficient in understanding of phases of clinical trials
Ability to work across satellite locations and provide on-site and remote support
Is competent and autonomous with minimal assistance and supervision.

KNOWLEDGE, SKILLS, AND ABILITIES REQUIRED:

Excellent organization and communications skills
Strong interpersonal skills with the ability to effectively interact with all levels of staff and externals contacts
Must be detail oriented and have the ability to follow-through
Ability to effectively manage time and prioritize workload
Must practice discretion and adhere to hospital confidentiality guidelines at all times
Must have computer skills including the use of Microsoft Office

MINIMUM JOB QUALIFICATIONS:

The position requires a bachelor’s degree, with 1 to 3 years of related experience preferred. Experience working in a medical or scientific research setting or comparable technology orientated business environment preferred. Performs primary duties with greater independence and has progressed to performing more advanced skill sets as directed.

SUPERVISORY RESPONSIBILITIES: Orients and assists in training new staff

PATIENT CONTACT: Minimal patient contact.

At Dana-Farber Cancer Institute, we work every day to create an innovative, caring, and inclusive environment where every patient, family, and staff member feels they belong. As relentless as we are in our mission to reduce the burden of cancer for all, we are committed to having faculty and staff who offer multifaceted experiences. Cancer knows no boundaries and when it comes to hiring the most dedicated and compassionate professionals, neither do we. If working in this kind of organization inspires you, we encourage you to .

Dana-Farber Cancer Institute is an equal opportunity employer and affirms the right of every qualified applicant to receive consideration for employment without regard to race, color, religion, sex, gender identity or expression, national origin, sexual orientation, genetic information, disability, age, ancestry, military service, protected veteran status, or other characteristics protected by law.

EEO Poster

Pay Transparency Statement

The hiring range is based on market pay structures, with individual salaries determined by factors such as business needs, market conditions, internal equity, and based on the candidate’s relevant experience, skills and qualifications.

For union positions, the pay range is determined by the Collective Bargaining Agreement (CBA).

$56,000.00 - $62,700.00

Apply Now

Refine Your Search

clinical research coordinator jobs in abington, ma

Clinical Research Coordinator II - Foxborough

Clinical Records Coordinator

Clinical Research Coordinator - Population Sciences

Clinical Research Coordinator - MEE

Clinical Research Coordinator I/II/III Opportunities – Multiple Locations Nationwide

Clinical Research Coordinator

Clinical Research Coordinator I

Clinical Research Coordinator - Neurosurgery Research

Sports Concussion Clinical Research Coordinator II

Clinical Research Associate II

Clinical Research Coordinator

Clinical Research Assistant

Clinical Research Coordinator I - Urology

Clinical Research Coordinator - Brighton

Clinical Research Coordinator - Thoracic Oncology

Clinical Administrative Coordinator

Clinical Research Coordinator II - Attleboro

Clinical Research Associate

Clinical Research Coordinator I

Clinical Research Coordinator

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