Clinical Research Associate I: Site Monitoring & Protocols
Allen Spolden
A leading clinical research organization based in Boston seeks a Clinical Research support specialist. The role involves assisting in protocol design, generating clinical documents, monitoring ongoing studies, and reporting findings. Ideal candidates will have a BA, BS, RN, or BSN degree and 1-2 years of clinical research experience. Strong attention to detail, multi-tasking ability, and excellent communication skills are essential. This position offers a chance to contribute significantly to clinical trials and their compliance. #J-18808-Ljbffr Allen Spolden
Vacancy posted 2 days ago
Similar jobs that could be interesting for youBased on the Clinical Research Associate I: Site Monitoring & Protocols in Boston, MA vacancy
- Alira Health Group is seeking a Clinical Research Associate to join its Boston team. The CRA will conduct site monitoring for clinical trials and ensure compliance with regulations. Responsibilities include overseeing trial management, coordinating with cross-functional...WebsiteRemote job
- Parexel is looking for a Senior Clinical Research Associate (Sr. CRA) in Boston, MA. The role involves managing site operations for clinical trials, ensuring patient safety... ...Candidates should have at least 3 years of monitoring experience, preferably in oncology. The Sr....Website
$53 - $69 per hour
...seeking a professional to support the Clinical Affairs team in ensuring compliance with... ...have 2+ years of experience in a clinical research setting, proficiency in Microsoft... ...in various responsibilities including site monitoring and maintenance of trial master files....WebsiteHourly payWork at office- ...Are you passionate about clinical research and ready to make an impact... ...for a Clinical Research Associate (CRA) to join a fast-... ...What You'll Do: Conduct site initiation, monitoring, and close-out visits to... ...Identify and escalate any protocol deviations, safety concerns...Website
CTTX Health
Cambridge, MA4 days ago - ...Responsible for providing Clinical Research support for all clinical trials... ...design and preparation of protocols and case report forms. Generate... ...of potential clinical sites according to established criteria... .... Conduct ongoing study monitoring, including frequent periodic...Website
Allen Spolden
Boston, MA7 days ago - ...healthcare intelligence and clinical research organisation united... ...according to protocol, regulatory requirements... ...lead on clinical trial monitoring tasks requiring... ...Monitoring clinical trial sites to ensure adherence... ...a Clinical Research Associate, with a strong understanding...WebsiteWork from home
ICON
Cambridge, MA2 days ago - ...preferred. Job Purpose: The Clinical Research Associate (CRA) has local... ...of the studies at allocated sites and is an active participant... ...has the responsibility for monitoring the study conduct to ensure... ...privacy breaches, Clinical Study Protocol (CSP) or ICH-GCP compliance...WebsiteLocal areaRemote workFlexible hoursShift work
PAREXEL
Boston, MA6 days ago $101.6k - $169.3k
...Senior Clinical Research Associate 1 IQVIA is hiring Senior Clinical Research Associate 1 with... ...respiratory: Job Overview: Perform monitoring and site management work to ensure that... ...study data as required by the study protocol, applicable regulations and...WebsiteFull timePart timeLocal areaImmediate startWorldwideIQVIA Holdings
Boston, MA2 days ago$84.5k
...striving for excellence in clinical research, turning science into medicine... ...with the investigator and site staff for meaningful and effective... ...the clinical trial program, protocol and patient treatment... ..., routine, and site closure monitoring activities with compliance to...WebsiteContract workTemporary workLocal areaAbbVie
Boston, MA3 days ago$110k
...Sr. Clinical Research Associate Date: Jun 17, 2026 Location: Boston, MA, US Company... ...Work: 1-2 days at home (site based) Salary Range: The... ...site activity for multiple protocols. Coordinates budgets and... ...timeliness of data collection. Monitoring study metrics and site...WebsiteTemporary workInterim roleRemote workWork from homeWorldwideFlexible hoursGetinge AB
Boston, MA1 day ago$105.6k - $158.4k
...eGenesis eGenesis is a clinical-stage biotechnology... ...a Senior Clinical Research Associate with 4+ years of experience monitoring complex clinical trials... ...managing investigative sites and conducting site qualification... ..., and study protocols. Proven ability to oversee...WebsiteInterim roleRemote workFlexible hoursShift workeGenesis Bio
Cambridge, MA5 hours ago- ...Conduct site monitoring visits in accordance with standards of practice guidelines and federal... ...study monitoring visits to assess protocol and regulatory compliance per the... ...degree. Experience At least 1-2 years of clinical research experience required. Previous...WebsiteWork at office
Mass General Brigham (Enterprise Services)
Boston, MA5 hours ago - ...Clinical Research Associate (CRA) Are you passionate about clinical research and ready to make... ...neuroscience. What You'll Do: Conduct site initiation, monitoring, and close-out visits to ensure... .... Identify and escalate any protocol deviations, safety concerns, or...Website
- ThermoFisher Scientific in Cambridge, MA, is seeking a Clinical Research Associate (Level II) to perform and coordinate clinical monitoring and site management processes. In this role, you’ll ensure adherence to protocols, conduct remote or on-site visits, and maintain...WebsiteRemote work
$110k - $135k
...currently seeking an Oncology Clinical Research Associate (CRA) for an opportunity in... ...Organization. Responsibilities Conduct site and study visits and perform all site monitoring activities across multiple... ...development of study tools, protocols, and clinical trial...WebsiteRemote work- ...integrated platform in terms of research and development, clinical development, manufacturing... ...Key Responsibilties Conduct site selection, initiation, routine monitoring, and close-out visits per ICH... ...monitoring. Track and report SAEs, protocol deviations, and elevate...WebsiteWorldwide
$85k - $125k
...of the Alira Health Clinical team. The CRA is highly... ...to conduct site monitoring responsibilities for... ...CRAs, in‑house CRAs, Associate Director of Clinical... ...Project Managers to ensure protocol compliance, address site... ...Knowledge of clinical research, ICH GCP and local regulations...WebsiteContract workInterim roleLocal areaRemote work$85k - $125k
Responsibilities Perform site monitoring visits (selection, initiation,... ...regulatory requirements, i.e. Good Clinical Practice (GCP) and... ...and expectations. Provide protocol and study related training to... ...Medidata as necessary. Support research sites with local...WebsiteContract workLocal areaRemote workFlexible hours- ...Provide support to Clinical Affairs team to assure study site selection and... ...and some on‑site monitoring. Project Details... ...study according to protocol and in compliance... ...experience in a clinical research setting at a CRO.... ...Practice Guidelines associated with CRA...WebsiteHourly payWork experience placementInterim roleWork at office
- ...Job Description Join Us as a Clinical Research Associate (Level II) - Make an Impact... ...at least 1 year of travel monitoring experience in Neurology!... ...the clinical monitoring and site management process. As a Clinical... ...on-site visits to assess protocol and regulatory compliance...WebsiteWork at officeRemote workHome officeNight shift
- The Senior Clinical Research Associate (Sr. CRA) is responsible for the site management, site monitoring and close-out of assigned clinical trials investigator sites to ensure... ...is responsible for the resolution of all protocol-related issues for assigned investigator...WebsiteLocal areaRemote work
- Mass General Brigham (Enterprise Services) in Boston is looking for a Clinical Research Monitor. This hybrid role requires conducting site monitoring visits to ensure compliance with protocols and regulatory standards. The ideal candidate should have at least 1-2 years...Website
$30 - $40 per hour
...Assistant Psychedelic Dosing Session Monitor Join Us in Shaping the Future of Clinical Research Adams Clinical is a leading clinical trial site network committed to accelerating the... ...Monitor, ensuring participant safety and protocol adherence throughout the trial. You'...WebsiteHourly payDaily paidReliefFlexible hours3 days per weekAdams Clinical
Boston, MA5 days ago$58.24k - $90k
# Clinical Trials MonitorBoston, MA • Beth Israel Deaconess... ...**The Clinical Trials Monitor (CTM) monitors and... ...-initiated clinical research studies across all disease... ...may require some on site work.**Job Description... ...of SOPs, study protocols and supporting documents...WebsiteFull timeWork experience placementWork at officeRemote workShift work$85k - $125k
...Health, based in Boston, is seeking a Clinical Research Associate to conduct monitoring visits and ensure compliance with... ...Responsibilities include training site staff and managing communication... ...the study process while ensuring protocol adherence. The position offers a salary...Website- Summary: The Senior Study Monitor provides centralized oversight of study quality... ...across up to 15 participating sites. This role ensures protocol adherence, data quality, and... ...adherence to IRB requirements and research Good Clinical Practices (GCP) guidelines Maintain...WebsiteRemote work
$65 - $76 per hour
...Lead Dosing Session Monitor Boston, Massachusetts, United States... ...Join Us in Shaping the Future of Clinical Research Adams Clinical is a leading clinical trial site network committed to... ..., in alignment with the study protocol and the training guidelines provided...WebsiteHourly payPart timeRemote work3 days per week- ...Clinical Research Associate Integrated Resources, Inc., is led by a seasoned... ...performs work within established protocols under general supervision.... ...etc.) being sent to sites prior to initiation as necessary... ...SOP. Reviews Clinical Monitoring Reports and correspondence...WebsiteContract work
Careers Integrated Resources Inc
Lexington, MA5 days ago $233k - $315k
...Department: 106750 Clinical Development Location: San Diego, USA-... ...The Senior Director, Medical Monitor & Safety Physician is a clinical... ...ensuring subject safety and protocol adherence. Conduct timely medical... ...with colleagues and/or on‑site in San Diego. No role is...WebsiteTemporary workRemote workTravere Therapeutics
Boston, MA1 day ago- ...Clinical Research Associate The Alliance for Clinical Trials in Oncology Foundation (Foundation) is... ...studies. This role is responsible for key site management and study start-up... ...site information and rosters; reviewing monitoring reports to identify deficiencies, reviewing...WebsiteRemote work
Alliance for Clinical Trials in Oncology Foundation
Boston, MA2 days ago
Do you want to receive more vacancies?
Subscribe and receive similar vacancies to Clinical Research Associate I: Site Monitoring & Protocols. Be the first to apply!
Related searches
- clinical research associate cra Boston, MA
- clinical research administrator Boston, MA
- clinical research associate Boston, MA
- clinical research assistant Boston, MA
- on-site clinical research associate (traveling/remote) Boston, MA
- clinical trials assistant Boston, MA
- pool monitor Boston, MA
- monitor Boston, MA
- patient monitor Boston, MA
- program monitor Boston, MA