Full-time
Clinical Research Coordinator - BIDMC Clinical Research Coordinator Pool
Competitive
Boston, MAScience & PharmaceuticalPosted 18d ago
You'll complete your application on the employer's website.
← Back to jobs
Role overview
Job type
Salary
Competitive
Location
Sector
Posted
18 days ago
Job description
Beth Israel Deaconess Medical Center is seeking a Clinical Research Coordinator with prior experience to support regulatory and patient-facing activities across a portfolio of assigned clinical trials. The successful candidate will support multiple concurrent clinical trials, ensuring rigorous compliance with federal, state, and institutional regulations while maintaining a high standard of participant care and engagement.
Tags
Health Care
Family & Care
Healthcare
Hospital
Professional Services
Education
Elder Care
Primary and Urgent Care
Training
Insider Connection @Beth Israel Lahey Health
2 email credits available today
Beyond your network
Responsibilities
Independently or in conjunction with other clinical research staff and/or research nurse, recruits and enrolls research subjects onto clinical research projects according to study protocols. May assess research subjects' eligibility for inclusion in a particular protocol based on contracts with physicians and nurses and knowledge of the protocol. (essential)
Checks all eligibility and ineligibility criteria with the research subjects' medical record. Verifies information with clinical research nurse and/or principal investigator. (essential)
Discusses informed consent with research subjects. Interacts with research subjects prior to entering the study and throughout the entire treatment. Assists with scheduling appointments and follow up tests. (essential)
Learns protocol and monitors strict adherence to protocols by physicians, nurses and research subjects. Reviews protocol requirements with physicians, nurses and fellows. Identifies any problems with protocol compliance and notifies principal investigator and/or research nurse. Begins to learn how to independently resolve problems with protocol. (essential)
Extracts data on protocol subjects from hospital records, outpatient charts and private physician office records in order to complete case report forms required by specific protocols. Enters data into computerized system. (essential)
Assists clinic staff in obtaining insurance approval for subject protocol participation and scheduling tests and arranging admissions or outpatient visits for subjects. (essential)
Assists investigator with correspondence with IRB. (essential)
As needed, may function in areas/clinics performing job duties related to clinical research studies
Preferred
Fluency in Spanish and Portuguese is strongly preferred
Benefits
Compensation may exceed the base hourly rate depending on shift differentials, call pay, premium pay, overtime pay, and other additional pay practices, as applicable to the position and in accordance with the law.
Beth Israel Lahey Health requires that all staff be vaccinated against influenza (flu) as a condition of employment.
Glassdoor
3.5
Beth Israel Lahey Health Center offers patient care, urgent care, assisted living, and research and education services.
Cambridge, Massachusetts, USA
https://www.bilh.org
Late Stage
Leadership Team
Avery Palardy
Executive Director, Climate & Sustainability
Robert Fields
EVP, Chief Clinical Officer
Recent News
Boston Globe
Beth Israel Lahey Health wins state OK for nearly $80 million Lahey Clinic expansion
2026-10-17
Healey is weak on the economy, but Minogue’s pitch isn’t landing with voters
2026-10-09
Beth Israel Lahey Health names next CEO to lead state’s second-biggest hospital system
Company data provided by
AI Tools
Customize Your Resume
Maximize your interview chances
Build Cover Letter
Make your application stand out
Analyze How Well You Fit
Understand your strength & weakness
Qualifications
Bachelor's degree required
1-2 years of related work experience required
Medical terminology
Working knowledge of computer systems required, including web-based applications and some Microsoft Office applications, which may include Outlook, Word, Excel, PowerPoint or Access
Fluency in Spanish and Portuguese is strongly preferred
1-2 years of related work experience required.
Required skills
Clinical Research Coordination, Regulatory Documentation, Informed Consent Process, Medical Terminology, Microsoft Outlook, Microsoft Word, Microsoft Excel, Microsoft PowerPoint, Microsoft Access, Data Entry, IRB Correspondence
Preferred skills
Fluency in Spanish and Portuguese is strongly preferred
Experience
1-2 years
Interested in this role?
Apply directly on the employer's website — it only takes a few minutes.
Similar vacancies
Other roles in Boston, MA or Science & Pharmaceutical
Prototyping Lab Technician, Robotics
Competitive
HealthcareFull-time
San FranciscoScience & PharmaceuticalsPosted 30+ Days Ago
You will work at the cutting edge of OpenAI's robotics hardware, partnering with hardware and software teams to develop, build, test, and iterate on robotic systems. Working closely with engineers, you will build prototypes, execute experiments, fabricate fixtures, troubleshoot hardware, and help drive rapid iteration…
HealthcareFull-time
USA - Torrance (205th Street)Science & PharmaceuticalPosted 25d ago
When you join us, you’ll be part of a global team harnessing the power of scientific testing and data-driven insights to build a healthier future. Clinical Research Coordinator Imagine your future with us At ALS, we encourage you to dream big.
Clinical Research Coordinator- Cardiac MRI Center
$21.64 - $26.50
HealthcareFull-time
BIDMC East CampusScience & PharmaceuticalPosted 26d ago
When you join the growing BILH team, you're not just taking a job, you’re making a difference in people’s lives. Responsible for screening research subjects for participation in clinical research projects, enrolling research subjects onto these studies, monitoring protocol implementation, completing required forms and reporting results.