20 Best clinical research associate jobs in Boston, MA (Hiring Now!)

Site Manager-Dorchester, MA
Care Access —Dorchester, MA
Act as a primary point of contact in the therapeutic field for Care Access Research. Ability and willingness to mentor and guide less experienced CRC as they…
Estimated: $78.3K - $99.1K a year
Quick Apply
Client Recovery Advisor (CRA)
Aware Recovery Care —Dorchester, MA
At Aware Recovery Care, you will give clients the tools to navigate their daily lives and help them on their own unique path to recovery.
$20 - $26 an hour
Quick Apply
4d
Principal Clinical Trial Manager - Early Phase
Syneos - Clinical and Corporate - Prod —United States
Reviews the content and quality of site and central monitoring documentation (site monitoring calls, site visit reports, site letters, central monitoring…
$178,601 - $210,900 a year
Clinical Study Manager (USA - REMOTE)
VivoSense Inc —Boston, MA
This is a multi-faceted role in which you will have the opportunity to lead the scientific offering on client projects including 1) driving all phases of…
$90,000 - $120,000 a year
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15h
Clinical Trial Associate
Deciphera Pharmaceuticals —Waltham, MA
May develop and maintain study documents. We are seeking a Clinical Trial Associate (CTA) to assist and provide support to the members of the clinical…
Estimated: $64.7K - $81.9K a year
Quick Apply
4d
Clinical Neurotechnology Research Assistant
Massachusetts General Hospital(MGH) —Boston, MA
Valid driver’s license required. These research sessions occur in the homes of clinical trial participants and may involve driving for up to three hours.
Estimated: $49.9K - $63.1K a year
2h
Research Assistant, Orthopedics (part time)
Boston Medical Center —Boston, MA
Performs office-related duties such as answering phones, picking up and delivering mail, ordering and distributing office supplies, handling faxes, scanning,…
Estimated: $32.3K - $40.8K a year
17h
Clinical Research Coordinator
Massachusetts General Hospital(MGH) —Somerville, MA
Major responsibilities of note include the identification, recruitment, and enrollment of study subjects, management of IRB documentation of the approved…
Estimated: $57K - $72.1K a year
2h
Clinical Research Coordinator II - Pediatric Cancer Predisposition
Dana-Farber Cancer Institute —Boston, MA
Maintains regulatory binders and ensures study compliance with all state, federal, and IRB requirements. Shows an understanding in setting up, coordinating and…
Estimated: $60.3K - $76.4K a year
20h
Clinical Research Associate II-Cancer Center Protocol Office
Massachusetts General Hospital(MGH) —Boston, MA
Less than 25% domestic travel (1-2 field visits per month maximum). Answer questions about eligibility, study procedures or data entry.
Estimated: $63.7K - $80.7K a year
Part-Time Clinical Research Coordinator II
Beth Israel Deaconess Medical Center —Brookline, MA
Responsible for screening patients for participation in clinical trials, enrolling patients onto these studies, monitoring protocol implementation, completing…
Estimated: $42.8K - $54.1K a year
4d
Clinical Research Assistant I- GI/Nutrition Dr. Scott Snapper's Lab
Boston Children's Hospital —Boston, MA
A Bachelor's degree in a scientific or health related field with 0-2 years of clinical and/or lab experience. Completing data entry for active studies.
Research Assistant I DOM Men's Health
Brigham & Women's Hospital(BWH) —Boston, MA
Help to implementation of clinical trial recruitment strategies and social media postings. Screen subjects over the telephone to determine their initial…
Estimated: $46.2K - $58.5K a year
3d
Clinical Research Coordinator - Brain Tumor Precision Medicine
Dana-Farber Cancer Institute —Boston, MA
Utilize REDCap, OncCore, Excel and other hospital information systems and statistical software analysis tools to perform clinical research and outcomes data…
Estimated: $60.3K - $76.4K a year
Clinical Operations Coordinator - Contractor
Outcomes4Me —Boston, MA
You will play a pivotal role in processing medical records in support of clinical data abstraction operations as well as to help us to deliver upon key company…
Estimated: $62.5K - $79.1K a year
RESEARCH ASSISTANT, School of Social Work, Administration
Boston University —Boston, MA
The RA will be responsible for study implementation activities including but not limited to: advertising, screening and recruiting eligible participants,…
Estimated: $46.8K - $59.3K a year
11d
Research Assistant I, Infectious Disease
Brigham & Women's Hospital(BWH) —Boston, MA
Answer any phone calls and inquiries regarding the study protocol. Per protocol instruction, conduct telephone interviews and schedule participants for study…
Estimated: $41.7K - $52.9K a year
Research Assistant II, Geriatrics
Boston Medical Center —Boston, MA
Performs office-related duties such as answering phones, picking up and delivering mail, ordering and distributing office supplies, handling faxes, scanning,…
Estimated: $37.5K - $47.5K a year
Clinical Research Specialist, GS
Brigham & Women's Hospital(BWH) —Boston, MA
The RS oversee the conduct and participate in associated research studies including study design, analysis, and manuscript preparation. Adult (26 to 54 years).
Estimated: $122K - $154K a year
Sr. Clinical Research Coordinator
Beth Israel Deaconess Medical Center —Boston, MA
Responsible for managing/overseeing the recruiting, screening and enrolling of patients for participation in multiple clinical trials, ensuring compliance with…
Estimated: $55.8K - $70.6K a year

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Site Manager-Dorchester, MA

Care Access - Dorchester, MA

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Job Details

Full-time Estimated: $78.3K - $99.1K a year

Benefits

Health savings account
Disability insurance
Health insurance
Dental insurance
401(k)
Paid time off
Vision insurance
Life insurance

Qualifications

Microsoft Word
Microsoft Excel
Clinical research
LVN
RN License
Phlebotomy
5 years
Writing skills
Research
IVR
Bachelor's degree
Clinical trials
Good Clinical Practice
Computer skills
LPN
Leadership
Communication skills
FDA regulations

Full Job Description

What We Do

Care Access is delivering the future of medicine today! Care Access has a revolutionary model that breaks down traditional barriers to clinical trials that limit participation among physicians and patients to 3%. By removing this bottleneck, Care Access is helping accelerate the approval and delivery of critical and life-saving therapies.

Who We Are

We care. Our people are the engines behind our mission: to revolutionize access to clinical trials for the benefit of patients everywhere. We care for one another, find new ideas to accelerate medicine, and seed a long-term impact for generations.

Position Overview

The Site Manager is responsible for the most pivotal and complex protocols and study designs being conducted at Care Access Research sites.

What You'll Be Working On

Duties include but not limited to:

Site Support Responsibilities:

Supports Key Sponsors and CROs
Manages some of the sites most challenging therapeutic areas and study designs
Able to monitor and mentor all levels of CRCs to ensure complete understanding of Care Access Research processes, SOPs and values, ensuring that a successful transition to more demanding opportunities and responsibilities
Assist Region Manager
Assist Region Manager in performing quality control check of all study source documents for completeness and quality

Therapeutic Responsibilities:

Demonstrate deep knowledge about the therapeutic area of responsibility
Demonstrate comprehensive understanding of related Protocol designs, outcomes and timelines
Engage in continuous independent learning within the therapeutic area of responsibility
Act as a primary point of contact in the therapeutic field for Care Access Research

Study Preparation:

Study Management:
Prioritize activities with specific regard to protocol timelines
Maintain adherence to FDA regulations and ICH guidelines in all aspects of conducting clinical trials.
Maintain effective relationships with study participants and other care Access Research personnel.
Interact in a positive, professional manner with patients, sponsor representatives, investigators and Care Access Research personnel and management.
Communicate clearly verbally and in writing.

Patient Coordination:
Prescreen study candidates
Obtain informed consent per Care Access Research SOP .
Complete visit procedures in accordance with protocol.
Train others and complete basic clinical procedures, such as blood draws, vital signs, ECGs, etc.
Review laboratory results, ECGs, and other test results (e.g., MRIs) for completeness and alert values, ensuring investigator review in a timely fashion.
Identify adverse events (AEs) and Serious Adverse Events (SAEs) and promptly notify Principal Investigator and Sponsor (where appropriate)

Documentation:
Record data legibly and enter in real time on paper or e-source documents
Accurately record study medication inventory, medication dispensation, and patient compliance.
Resolve data management queries and correct source data within sponsor provided timelines
Assist regulatory personnel with completion and filing of regulatory documents.
Perform other duties as assigned. The duties and responsibilities listed above are representative of the nature and level of work assigned and are not necessarily all-inclusive.
Physical and Travel Requirements
This is an on-site position with regional commute requirements. Regularly planned travel within the region will be required as part of the role.

Perform other duties as assigned. The duties and responsibilities listed above are representative of the nature and level of work assigned and are not necessarily all-inclusive

What You Bring

Role Requirements:

Knowledge, Skills and Abilities:

Excellent working knowledge of medical and research terminology
Excellent working knowledge of federal regulations, good clinical practices (GCP)
Understanding of issues affecting clinical research in the identified therapeutic area of expertise
Ability and willingness to mentor and guide less experienced CRC as they develop and gain experience in all therapeutic areas
Ability to communicate and work effectively with a diverse team of professionals
Excellent organizational, prioritization and leadership skills and capabilities with a strong attention to detail
Excellent computer skills with demonstrated abilities using clinical trials database, IVR systems, electronic data capture, MS word and excel
Critical thinker and problem solver
Excellent interpersonal skills, detailed oriented and meticulous
Friendly, outgoing personality with the ability to maintain a positive attitude under pressure
High level of self-motivation and energy
Excellent professional writing and communication skills
Ability to work independently in a fast-paced environment with minimal supervision

Certifications/Licenses, Education, and Experience:

RN or LPN/LVN preferred
Research Professional Certification- CRCC preferred
Bachelor’s Degree preferred, or equivalent combination of education, training and experience.
A minimum of 5 years experience as a Clinical Research Coordinator requied
Prefer1 year of experience as a Care Access Research Clinical Research Coordinator
Recent phlebotomy experience required

Benefits (US Full-Time Employees Only)

PTO/vacation days, sick days, holidays.
100% paid medical, dental, and vision Insurance. 75% for dependents.
HSA plan
Short-term disability, long-term disability, and life Insurance.
Culture of growth and equality
401k retirement plan

Diversity & Inclusion

We serve patients and researchers from diverse cultures and communities around the world. We are stronger and better when we build a team representing the people we aim to support. We maintain an inclusive culture where people from a broad range of backgrounds feel valued and respected as they contribute to our mission. We value diversity and believe that unique contributions drive our success.

At Care Access, every day, we are advancing medical breakthroughs. We’re uniting standard patient care with cutting-edge treatments and research. Our work brings life-changing therapies to those in need and paves the way for newer and greater treatments to reach the world. We’re proud to advance these breakthroughs and work with the big players while engaging with the best

physicians and caring for patients. Our team of experts is paving the way to take this vision forward through innovation and a unique technology-enabled.

We are an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity or expression, pregnancy, age, national origin, disability status, genetic information, protected veteran status, or any other characteristic protected by law.

Care Access currently is unable to sponsor work visas.

Employment Statement

Care Access complies with all employment laws and regulations with respect to its employment practices, terms and conditions of employment, and pay equity and wages. Care Access does not engage in any unfair or forced labor practice and does not tolerate, under any circumstances, the use of any form of forced or involuntary labor, child labor, or human trafficking. This extends to suppliers, partners, or other third parties with whom Care Access does business. Care Access values and promotes the protection of human rights everywhere.

Job Type: Full-time

Quick Apply

clinical research associate jobs in Boston, MA

Site Manager-Dorchester, MA

Client Recovery Advisor (CRA)

Principal Clinical Trial Manager - Early Phase

Clinical Study Manager (USA - REMOTE)

Clinical Trial Associate

Clinical Neurotechnology Research Assistant

Research Assistant, Orthopedics (part time)

Clinical Research Coordinator

Clinical Research Coordinator II - Pediatric Cancer Predisposition

Clinical Research Associate II-Cancer Center Protocol Office

Part-Time Clinical Research Coordinator II

Clinical Research Assistant I- GI/Nutrition Dr. Scott Snapper's Lab

Research Assistant I DOM Men's Health

Clinical Research Coordinator - Brain Tumor Precision Medicine

Clinical Operations Coordinator - Contractor

RESEARCH ASSISTANT, School of Social Work, Administration

Research Assistant I, Infectious Disease

Research Assistant II, Geriatrics

Clinical Research Specialist, GS

Sr. Clinical Research Coordinator

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