Clinical Research Associate: Monitoring & Site Liaison
Hengrui Pharma
Hengrui Pharma is seeking a candidate based in Boston, Massachusetts for a role focused on clinical site monitoring. Responsibilities include performing site assessments, training investigative sites, and ensuring compliance with project requirements. The ideal candidate should have a Master's degree in Clinical Medicine or Pharmacy, be proficient in site monitoring workflows, and possess strong communication and execution skills. #J-18808-Ljbffr
- ...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...Website
$105.6k - $158.4k
...biotechnology company in Cambridge, MA, is seeking a Senior Clinical Research Associate with 4+ years of experience. You will be responsible for monitoring clinical trials, ensuring data integrity, and training investigative sites. Ideal candidates will have a background in ICH-...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$110k - $135k
...Piper Companies is currently seeking an Oncology Clinical Research Associate (CRA) for an opportunity in Boston,... ...Research Organization. Responsibilities Conduct site and study visits and perform all site monitoring activities across multiple study Responsible for...WebsiteRemote work- ...Qualifications Key Responsibilities: Conduct monitoring activities including investigative site feasibility assessment, site... ...and facilitate communication and liaison between the project management... ...Background Master’s degree in Clinical Medicine, Pharmacy or other...WebsiteImmediate start
- ...Are you passionate about clinical research and ready to make an impact on patients' lives... ...looking for a Clinical Research Associate (CRA) to join a fast-growing biotech... ...neuroscience. What You'll Do: Conduct site initiation, monitoring, and close-out visits to ensure...Website
- ...on 03/29/2024 Responsible for providing Clinical Research support for all clinical trials. Under... ...in the evaluation of potential clinical sites according to established criteria of... ...necessary materials. Conduct ongoing study monitoring, including frequent periodic site...Website
$120k - $140k
...Remote Senior Clinical Research Associate (CRA) – Oncology Salary: $120,000 - $140,000 per year Prep-... ...Responsibilities Develops strong investigative site relationships and ensures continuity... ...visits, initiation visits, interim monitoring visits, and close‑out visits to...WebsiteInterim roleLocal areaRemote workFlexible hours- Clinical Research Associate, Sponsor Dedicated ICON plc is a world-leading healthcare intelligence... ...You will contribute to clinical trial monitoring activities, taking responsibility for... ...responsibilities include: Conducting site qualification, initiation, monitoring...WebsiteFlexible hours
$101.6k - $169.3k
...Senior Clinical Research Associate 1 Experience in oncology, cardiovascular, renal, metabolic, CNS, Obesity (GLP-1), diabetes, GI, MASH/NASH... ..., or respiratory is required. Job Overview Perform monitoring and site management work to ensure that sites are conducting the...WebsiteFull timePart timeLocal areaImmediate start$45 - $55 per hour
...responsibility for coordinating clinical monitoring activities, overseeing CRO clinical/site management, and co-monitoring... ...meetings with Medical Science Liaisons. Monitor clinical study activities... ...Manufacturing and Biotechnology Research #J-18808-Ljbffr...WebsiteContract workFlexible hours- ...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 patient safety and quality study execution in accordance with applicable prevailing laws, Good...WebsiteLocal areaRemote work
- ...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
$85k - $125k
...member of the Alira Health Clinical team. The CRA is highly motivated... ...independently to conduct site monitoring responsibilities for... ...activities, or act as the primary liaison between site and Central Monitor... ...as necessary. Supports research sites with local Institutional...WebsiteContract workWork at officeLocal areaRemote workFlexible hours- ...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... ...regulatory inspections in liaison with LSAD and Clinical Quality...WebsiteLocal areaRemote workFlexible hoursShift work
$105.6k - $158.4k
...About eGenesis eGenesis is a clinical-stage biotechnology company developing... ...is seeking a Senior Clinical Research Associate with 4+ years of experience monitoring complex clinical trials in pharmaceutical... ...managing investigative sites and conducting site qualification...WebsiteInterim roleRemote workFlexible hoursShift work$84.5k
...pipeline by striving for excellence in clinical research, turning science into medicine for our... ...Partners with the investigator and site staff for meaningful and effective engagements... ...training, routine, and site closure monitoring activities with compliance to the protocol...WebsiteContract workTemporary workLocal area- ...is seeking a skilled professional for clinical research roles in Boston, MA. In this position,... ...the primary contact for investigative sites, ensuring compliance with clinical trial... ...year of experience in clinical research monitoring and holds a relevant tertiary qualification...Website
$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...WebsiteRemote work- ...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 patient safety and quality. Applicants should have a Bachelor's degree...Website
- ...seeking a qualified individual to conduct site monitoring visits in Boston. This role ensures the... ...and verifies data accuracy for clinical trials. The ideal candidate will have a... ...Bachelor's degree and 1-2 years of clinical research experience, with a strong attention to...Website
- ...A major healthcare organization located in Boston seeks a Clinical Research Associate to ensure compliance through site monitoring visits and to protect human subjects during clinical trials. You'll be responsible for reviewing documentation, conducting training, and...Website
- ...metric for minimum required days on site per month. Opportunity for cross... ...positions Lead CRA, CRA Manager, Clinical Trial Manager Airline club allowance... ...Conduct qualification, initiation, monitoring, and closeout visits for research sites in compliance with the...WebsiteContract workCasual workLocal areaImmediate startWork from homeVisa sponsorshipFlexible hours
$110k - $135k
...Piper Companies is currently seeking an Oncology Clinical Research Associate (CRA) for an opportunity in Boston,... ...Research Organization. Responsibilities Conduct site and study visits and perform all site monitoring activities across multiple study Responsible for...WebsiteRemote work$84.5k - $162k
...Clinical Research Associate Advance AbbVie's pipeline by striving for excellence in clinical research... .... Partners with the investigator and site staff for meaningful and effective... ...training, routine, and site closure monitoring activities with compliance to the protocol...WebsiteContract workTemporary workWork at officeLocal areaImmediate start$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...WebsiteHourly payPrice workExtra incomeFull timeFor contractorsFreelanceLive inFlexible hours$74.9k - $82.4k
...The Clinical Trials Monitor helps to ensure compliance of the clinical research enterprise with all related regulatory policies and guidelines, including federal, state,... ...through a combination of remote data review and on site monitoring visits. Some travel will be required...WebsiteWork at officeLocal areaRemote work$50.5k - $82.01k
...Site: Mass General Brigham Incorporated Mass General Brigham is a not‑for‑profit organization... ...that supports patient care, research, teaching, and community service. We seek a Clinical Research Associate to conduct site monitoring visits in accordance with standards of...WebsiteRemote workShift work3 days per week- ...Mileage will be reimbursed.67 cents per mile for travel between sites, based upon completed mileage form and subject to the... ...is in working order and request repair, if indicated Field monitors may be required to transfer supplies from Central Warehouse or...WebsiteHourly payTemporary workSummer workSeasonal workMonday to FridayShift work
$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
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