20 Best clinical research associate jobs in Cambridge, 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: $84.2K - $107K a year
Quick Apply
Interim Skilled Nursing Facility Clinical Manager/Documentation Regulatory Specialist
Kirby Bates Associates —Massachusetts
Massachusetts RN license required (Massachusetts is not a compact state). The complex provides amenities including a library, dry cleaning, barber shops, an…
$195,000 - $208,000 a year
Quick Apply
Clinical Research Assistant II-Primary Care Center
Boston Children's Hospital —Boston, MA
The Research Assistant will work closely with various researchers and other practice staff with all aspects of study design and implementation, including…
Client Recovery Advisor (CRA)
Aware Recovery Care —Melrose, 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
Senior Clinical Research Associate
JDA —Bedford, MA
Strong knowledge of clinical trials, clinical development, and clinical research processes. Assist in the development and implementation of clinical trial…
$80,000 - $105,000 a year
Quick Apply
Senior Clinical Trial Manager
Warman O'Brien —Waltham, MA
Science or healthcare bachelor’s degree required. The ideal candidate will have the minimum of a B.S. degree in science or healthcare and have At least 4 years…
$120,000 - $150,000 a year
Quick Apply
10d
Senior Clinical Trial Associate
Replimune, Inc. —Woburn, MA
Assist in updates for all clinical trials tracking tools for Trial Master File (TMF), monitoring visits, enrollment, laboratory samples and clinical trial…
Estimated: $76.8K - $97.2K a year
2d
Clinical Research Associate III
BRIOHEALTH SOLUTIONS INC —Boston, MA
B.S. or higher degree in a science related field, or equivalent industry experience. Knowledge of principles of clinical research study design and approaches to…
Estimated: $112K - $142K a year
Quick Apply
Senior Clinical Trial Associate
Kymera Therapeutics —Watertown, MA
Kymera is a clinical-stage biotechnology company pioneering the field of targeted protein degradation (TPD) to develop medicines that address critical health…
Estimated: $71.3K - $90.2K a year
Quick Apply
Clinical Research Associate- Ophthalmology
Tufts Medical Center —Boston, MA
Records test results accurately and timely, inpatient hospital records, case report forms, and MD's own record (clinic charts). Experience with clinical trials.
Estimated: $58.7K - $74.3K a year
Quick Apply
3d
Clinical Research Associate
Massachusetts General Hospital(MGH) —Boston, MA
An advanced degree in psychology or social work. Working knowledge of clinical research protocols. The CRA will deliver the study intervention to participants.
Estimated: $65.4K - $82.8K a year
Senior Clinical Trial Associate
Progenics Pharmaceutical Inc —Bedford, MA
Education: Bachelor’s degree in science or related field. Develop, setup, and maintain study tracking tools for assigned trials to monitor study progress.
Estimated: $80.8K - $102K a year
Quick Apply
9d
Sr Clinical Research Associate (CRA)
ProKidney —Boston, MA
Tracks incoming and outgoing clinical and regulatory documents and updates for investigator sites. Maintain communication between the sponsor and all existing…
Estimated: $130K - $164K a year
Quick Apply
Senior Clinical Research Associate
Philips —Cambridge, MA
Owning the overall study process and adherence to clinical trial procedures by keeping oversight, identifying possible problems/risks, creating mitigation plans…
Estimated: $127K - $161K a year
Clinical Trial Assistant
Vericel Corporation —Cambridge, MA
Associate’s degree in life sciences, health informatics, or related field. Prepares investigator site files, trial master files (TMF) and electronic trial…
Estimated: $56.1K - $71K a year
Quick Apply
Clinical Research Coordinator I
Massachusetts General Hospital(MGH) —Somerville, MA
You must be able to work independently in a dynamic environment, juggle and prioritize multiple tasks, feel comfortable working with clinical and non-clinical…
Estimated: $64.2K - $81.3K a year
12d
Clinical Research Associate/Coordinator-Cancer Center Protocol Office
Massachusetts General Hospital(MGH) —Boston, MA
Maintain point of contact communication with enrolled patients and assist with front line questions regarding study participation.
Estimated: $60.6K - $76.7K a year
5d
Administrative Coordinator (Clinical Research Center/Pediatric Research)
Joslin Diabetes Center —Boston, MA
Provide routine and more complex administrative support such as: directing phone calls and faxes, coordinating maintenance of office machines, taking and…
$22 - $25 an hour
Quick Apply
Clinical Trial Associate
Ipsen Bioscience, Inc. —Cambridge, MA
Coordinate the dispatch order for the clinical supplies if not managed by a dedicated system such as IVRS, meaning the collection of appropriate documents…
$65,250 - $95,700 a year
Clinical Trials Associate
Monte Rosa Therapeutics, Inc —Boston, MA
Ability to collaborate effectively with cross functional team members and external partners. BA/BS degree required with a minimum of 2 years relevant clinical…
Estimated: $64.7K - $82K a year
6d

I want to receive the latest job alert for clinical research associate in Cambridge, MA

By signing in to your account, you agree to SimplyHired's Terms of Service and consent to our Cookie and Privacy Policy.

Site Manager-Dorchester, MA

Care Access - Dorchester, MA

Quick Apply

Job Details

Full-time Estimated: $84.2K - $107K 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.

Job Type: Full-time

Quick Apply

clinical research associate jobs in Cambridge, MA

Site Manager-Dorchester, MA

Interim Skilled Nursing Facility Clinical Manager/Documentation Regulatory Specialist

Clinical Research Assistant II-Primary Care Center

Client Recovery Advisor (CRA)

Senior Clinical Research Associate

Senior Clinical Trial Manager

Senior Clinical Trial Associate

Clinical Research Associate III

Senior Clinical Trial Associate

Clinical Research Associate- Ophthalmology

Clinical Research Associate

Senior Clinical Trial Associate

Sr Clinical Research Associate (CRA)

Senior Clinical Research Associate

Clinical Trial Assistant

Clinical Research Coordinator I

Clinical Research Associate/Coordinator-Cancer Center Protocol Office

Administrative Coordinator (Clinical Research Center/Pediatric Research)

Clinical Trial Associate

Clinical Trials Associate

Job Seeker Tools

Employer Tools

Browse

Stay Connected