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
$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-... ..., ensuring proper adherence to protocols. Competitive compensation packages...Website- ...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
- ...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
- ...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
- ...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
- Clinical Research Associate, Sponsor Dedicated ICON plc is a world-leading healthcare... ...to clinical trial monitoring activities, taking responsibility... ...include: Conducting site qualification, initiation,... ...clinical trials. Ensuring protocol compliance, data integrity,...WebsiteFlexible hours
$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- ...Conduct site monitoring visits in accordance with standards of practice guidelines and federal... ...study monitoring visits to assess protocol and regulatory compliance per the... ...Experience At least 1-2 years of clinical research experience required Previous...WebsiteWork at office
- Job Purpose The Senior Clinical Research Associate (Sr. CRA) is responsible for the site management, site monitoring and close‑out of assigned clinical trials investigator sites... ...is responsible for the resolution of all protocol‑related issues for assigned investigator...WebsiteLocal areaRemote work
$85k - $125k
...member of the Alira Health Clinical team. The CRA is highly motivated... ...independently to conduct site monitoring responsibilities for... ...Project Managers to ensure protocol compliance, address site questions... ...medidata as necessary. Supports research sites with local...WebsiteContract workWork at officeLocal areaRemote workFlexible hours$101.6k - $169.3k
Senior Clinical Research Associate 1 Experience in oncology, cardiovascular, renal, metabolic, CNS... ...is required. Job Overview Perform monitoring and site management work to ensure that sites... ...data as required by the study protocol, applicable regulations and guidelines...WebsiteFull timePart timeLocal areaImmediate start$131k - $150k
Sr. Clinical Research Associate About Servier Servier in the U.S. is a Boston-based, commercial... ...the effective management and monitoring of clinical studies in the site(s) assigned by the Clinical... ...Manager (COPM), while respecting the protocol and in accordance with the...WebsiteContract workTemporary workLocal areaRemote workFlexible hours- Parexel is seeking a Senior Clinical Research Associate (Sr. CRA) in Boston, Massachusetts. The Sr. CRA will be responsible for site management, monitoring, and close-out of clinical trials, ensuring... ...of clinical guidelines and protocols. Travel of 60-80% is expected. #J...Website
- ...The Alliance for Clinical Trials in Oncology Foundation... ...cancer clinical research and address important... ...seeking a Clinical Research Associate (CRA) to support the... ...is responsible for key site management and study start... ...rosters; reviewing monitoring reports to identify...WebsiteWork at officeFlexible hours
- ...Join our team as an ASE Attendance Monitor-a role perfect for someone who thrives in a detail-oriented, fast-paced environment where accuracy... ...to ensure student safety and correct counts. • Support the site supervisor in organizing daily enrichment and club activities: confirm...WebsitePart timeMonday to FridayShift work
- ...coordinates daily activities and operations of clinical research studies. Responsible for screening and enrolling patients, monitoring protocol implementation, completing required forms... ...research studies, conducted at both on site and off-site locations, guiding and...Website
- ...regulatory requirements for clinical trials are met. This position... ...regulations governing clinical research. Does this position require... ...binders. Prepare and submit protocol amendments, continuing reviews... ...entities. Participate in monitoring visits and maintain a record...WebsiteContract work
$45 - $55 per hour
...the position Take responsibility for coordinating clinical monitoring activities, overseeing CRO clinical/site management, and co-monitoring assigned international... ...Pharmaceutical Manufacturing and Biotechnology Research #J-18808-Ljbffr Integrated Resources, Inc ( IRI )WebsiteContract workFlexible hours$110k - $135k
A leading Clinical Research Organization is seeking an Oncology Clinical Research Associate (CRA) for a position in Boston, Massachusetts. The CRA will be responsible for conducting site and study visits, and monitoring activities both remotely and on-site. Candidates must...WebsiteRemote job$60 - $70 per hour
...Microbiology General Summary: The Environmental Monitoring and Utilities Monitoring Technical support... ...standards. This role reports to the Associate Director of Quality Control in Cell and Genetic Therapies (VCGT). on site role. 12 month contract with the chance to...WebsiteContract work$25 - $35 per hour
...routing, schedule, and territory. Efficiency: Standard inspections are designed for speed, typically requiring only 5-6 minutes on-site. Consistency: Enjoy stable, month-to-month volume in your assigned county. Workflow & Responsibilities Determine property occupancy...WebsiteHourly payPrice workExtra incomeFull timeFor contractorsFreelanceLive inFlexible hours- ...Gym Monitor The Gym Monitor position is an exciting opportunity for individuals who are passionate about healthy lifestyles and enjoy... ...in Massachusetts. Through our network of facilities and program sites, the YMCA provides health and wellness programming, child care,...WebsitePart timeSummer work
- ...direction of the Chief Epilepsy Monitoring Technologist and the Medical... .../EEG data and correlates the clinical and electrographic activity... ...various pieces of equipment on site and remotely. Identify... ...Diploma or Equivalent required or Associate's Degree Related Field of...WebsiteRemote workShift workWeekend work
$76.03k - $98.83k
Photo Editor, The Christian Science Monitor Job Category : The Christian Science Monitor... ...drafts for the department’s awareness; Researches and assigns photo shoots; Receives and... ...for publication; Searches news services sites to locate the best /most relevant photos...WebsiteFull timeImmediate start$60 - $70 per hour
...methodologies. The candidate should possess at least 7 years of industry experience and a Bachelor's degree in Microbiology. The role offers a pay range of $60-$70 per hour and is a 12-month on-site contract with potential for extension. #J-18808-Ljbffr Vertex PharmaceuticalsWebsiteHourly payContract work$79k - $100k
Public Health Consultant - Monitoring, Evaluation & Quality Improvement Type Full time Description Founded in 2004, BME Strategies is a... ...Working Conditions Remote work, with occasional travel to client sites, conferences, or meetings as required. Ability to work...WebsiteFull timeTemporary workLocal areaRemote workVisa sponsorshipWork visa$110k - $125k
Sr. Clinical Research Associate Location: Boston, MA, US Remote Work: 1-2 days at home (site based) Company: Paragonix Technologies, Inc. Salary... ...activity for multiple protocols. Coordinates budgets and... ...timeliness of data collection. Monitors study metrics and site...WebsiteTemporary workInterim roleRemote workWork from homeFlexible hours- ...Senior Medical Director, Clinical Development (Medical Monitoring) About the Company Rapidly growing organization... ...point of contact for investigative sites and sponsors, and providing real-... ...practical experience in medical research or clinical development. A minimum...Website
- Alira Health Boston, LLC is seeking a Clinical Research Associate who will play a vital role in the monitoring of clinical trials. Responsibilities include conducting site evaluations, ensuring adherence to protocols, and collaborating with clinical teams to enhance project...Website
$90k - $157.5k
...are looking for This role is the Digital Asset Transaction Monitoring Lead Analyst supporting the design and deployment of suspicious... ...and role requirements. Our standard hybrid model is 4 days on site and 1 day remote. Preferred location is Boston or Quincy, MA. We...WebsiteTemporary workWork at officeRemote workWork from homeFlexible hours
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