Clinical Research Associate — Site Start-Up & Compliance
Alliance for Clinical Trial in Oncology Foundation
The Alliance for Clinical Trials in Oncology Foundation is seeking a Clinical Research Associate (CRA) to manage clinical trial operations across AFT studies in Boston, Massachusetts. Responsibilities include overseeing site management, assisting with study start-up activities, and ensuring compliance with ICH GCP guidelines. The ideal candidate will have a BA/BS degree, relevant experience in biotech or clinical research, and proficiency with CTMS and eTMF systems. Benefits include 8 weeks paid time off, health plans, and tuition reimbursement. #J-18808-Ljbffr Alliance for Clinical Trial in Oncology Foundation
- Experienced Clinical Research Associate - Full-Service Syneos Health is a leading fully integrated biopharmaceutical... .... Job Responsibilities Performs site qualification, site initiation,... ...Practice (GPP) and protocol compliance. Uses judgment and experience to evaluate...WebsiteContract workInterim roleLocal areaImmediate startRemote workFlexible hours
- ...Clinical Research Associate The Alliance for Clinical Trials in Oncology Foundation (Foundation... ...role is responsible for key site management and study start-up activities, including... ...ensure studies are conducted in compliance with ICH GCP guidelines and organizational...WebsiteRemote work
- ...preferred. Job Purpose: The Clinical Research Associate (CRA) has local... ...of the studies at allocated sites and is an active participant... ...sites in clinical studies, in compliance with Client Procedural Documents... ...are accountable for study start-up and regulatory maintenance....WebsiteLocal areaRemote workFlexible hoursShift work
$45 - $55 per hour
...responsibility for coordinating clinical monitoring activities,... ...CRO clinical/site management, and co-... ...oversight: Oversee study start-up, working closely with... ...acquisitions or licensed assets. Compliance and safety: Adhere to... ...and Biotechnology Research #J-18808-Ljbffr...WebsiteContract workFlexible hours$105.6k - $158.4k
...eGenesis eGenesis is a clinical-stage biotechnology... ...seeking a Senior Clinical Research Associate with 4+ years of... ...managing investigative sites and conducting site... ...visits, while ensuring compliance with ICH-GCP,... ...Skilled in supporting site start-up, training investigators...WebsiteInterim roleRemote workFlexible hoursShift work$20 - $25 per hour
Join Us in Shaping the Future of Clinical Research Adams Clinical is a leading clinical trial site network committed to accelerating the development of life‑changing... ...activities and accurate documentation in compliance with ICH‑GCP, study protocols, and regulatory requirements...WebsiteHourly payWork at officeFlexible hours- ...Are you passionate about clinical research and ready to make an impact on patients' lives? We're looking for a Clinical Research Associate (CRA) to join a fast-growing biotech company (confidential... .... What You'll Do: Conduct site initiation, monitoring, and close-out...Website
- ...Job Title Responsible for providing Clinical Research support for all clinical trials. Under the direction of supervisor or designee,... ...guidelines. Participate in the evaluation of potential clinical sites according to established criteria of acceptability....Website
$20.16 - $29.01 per hour
...Site: The General Hospital Corporation Mass General Brigham... ...business people, tech experts, researchers, and systems analysts to... ...regulatory requirements for clinical trials are met. This position... ...detail. - Ability to recognize compliance and data integrity issues and...WebsiteHourly payContract workRemote work$99k - $121k
...Clinical Research Associate (CRA) Position Ardelyx is a commercial-stage biopharmaceutical... ...execution with an focus on site performance, data quality, and regulatory compliance. Building on prior experience... ...strategies Support study start-up, conduct, and close-out...WebsiteFull timeRemote workFlexible hours- Clinical Research Associate, Sponsor Dedicated ICON plc is a world-leading healthcare intelligence... ...responsibilities include: Conducting site qualification, initiation, monitoring... ...trials. Ensuring protocol compliance, data integrity, and patient safety throughout...WebsiteFlexible hours
- ...The Clinical Research Associate (CRA) is responsible for the site management, site monitoring and close-out of assigned clinical trials investigator sites to ensure... ...sites (e.g. patient safety, site quality and compliance with GCP), to maintain investigator and site staff...WebsiteLocal areaRemote work
$55k - $70k
Alira Health Group is seeking an In-house Clinical Research Associate to manage clinical sites in Boston. This role involves supporting sites from approval... ...-out with a focus on data integrity and regulatory compliance. The ideal candidate will have a Bachelor’s degree...WebsiteRemote job$110k - $135k
Overview Piper Companies is currently seeking an Oncology Clinical Research Associate (CRA) for an opportunity in Boston, Massachusetts (MA). The... ...leading Clinical Research Organization. Responsibilities Conduct site and study visits and perform all site monitoring activities...WebsiteRemote work- A leading clinical research organization based in Boston is seeking a Clinical Research Associate (CRA) to support clinical trial operations across AFT studies. The ideal candidate will manage site operations and facilitate compliance with ICH GCP guidelines. Responsibilities...Website
$55k - $70k
Alira Health Group is searching for an In-House Clinical Research Associate to manage and support clinical sites from approval to close-out. You will work closely with field CRAs and Project Managers to ensure the integrity of trial data without frequent travel. We are...WebsiteRemote job$67.5k - $99k
...Administrator page is loaded## Clinical Trial... ...medical need through research and innovation. Our passionate... ...up for the country and site binders and the trial... ...disclosure of expenses in compliance with regulations in... ...requested prior to the study start-up and during the course...WebsiteContract workTemporary workWork experience placementLocal area$101.6k - $169.3k
Senior Clinical Research Associate 1 Experience in oncology, cardiovascular, renal, metabolic, CNS, Obesity (GLP-1), diabetes, GI, MASH/NASH, dermatology... ...is required. Job Overview Perform monitoring and site management work to ensure that sites are conducting the study...WebsiteFull timePart timeLocal areaImmediate start- ...pipeline by striving for excellence in clinical research, turning science into medicine for our... ...performance. Partners with the investigator and site staff for meaningful and effective... ...driving improvement in data integrity, compliance, overall study performance and customer...WebsiteContract workTemporary workLocal area
$110k - $125k
Sr. Clinical Research Associate Location: Boston, MA, US Remote Work: 1-2 days at home (site based) Company: Paragonix Technologies, Inc. Salary: Minimum $110,000 - Maximum $125,000 plus 10% annual bonus. Position Overview The Senior Clinical Research Associate oversees...WebsiteTemporary workInterim roleRemote workWork from homeFlexible hours- A leading clinical research organization based in Boston seeks a Clinical Research support specialist. The role involves assisting in protocol... .... This position offers a chance to contribute significantly to clinical trials and their compliance. #J-18808-Ljbffr Allen SpoldenWebsite
$105.6k - $158.4k
...company in Cambridge, MA, is seeking a Senior Clinical Research Associate with 4+ years of experience. You will be... ...data integrity, and training investigative sites. Ideal candidates will have a background in ICH-GCP compliance and strong problem-solving skills. The role...Website- ...located in Boston, is seeking a dedicated Clinical Research Associate to advance AbbVie’s pipeline by... ...engaging effectively with investigative sites. The ideal candidate has at least one... ..., monitoring trials, and ensuring compliance with regulatory standards. We offer competitive...Website
$101.6k - $169.3k
A global clinical research organization is seeking a Senior Clinical Research Associate in Boston to oversee oncology study monitoring and site management. This role demands at least 2 years of on-site monitoring experience, along with a Bachelor's degree in a scientific...Website- ...Clinical Research Associate Integrated Resources, Inc., is led by a seasoned team with combined decades in the industry. We deliver strategic... ....g. lab kits, test machines, equipment etc.) being sent to sites prior to initiation as necessary. Provides oversight of...WebsiteContract work
- ...Clinical Research Registered Nurse (PT Weekday) Alcanza is a growing multi-site, multi-phase clinical research company with a network... ...the study protocol and in compliance with GCP, ICH, HIPAA, FDA Regulations... ...activities for study start-up, including completing...WebsiteFull timeTemporary workWeekday work
- A major healthcare provider in Boston is seeking a Research Assistant to support clinical research activities. The ideal candidate will possess a Bachelor's degree in a relevant field, have experience in clinical research, and excel in communication. Responsibilities include...WebsiteFull time
- ...supervision, coordinates daily activities and operations of clinical research studies. Responsible for screening and enrolling patients, monitoring... .../patients in the research studies, conducted at both on-site and off-site locations, guiding and advising them throughout...Website
- ...Parenteral Nutrition Program is seeking a Clinical Research Assistant to support day-to-day study... ...of its kind and serves as a major site in this 52-week multi-center randomized... ...evaluating DEFENCATH in reducing central-line associated bloodstream infections (CLABSIs) in...Website
- Job Title: Clinical Trial Administrator Location: Boston... ...is an experienced or associate level (junior level)... ...performing a variety of research, database, and... ...tracking vendor payments in compliance with federal regulations... ...CRO and Investigative sites for regulatory...WebsiteContract workWork experience placementLocal areaFlexible hours
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