Senior CRA: Site Monitoring & Trial Excellence
Parexel
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 in life sciences, at least 3 years of relevant monitoring experience, and preferably experience in oncology. The role involves significant collaboration with site and study teams, requiring excellent communication skills and a thorough understanding of clinical guidelines and protocols. Travel of 60-80% is expected. #J-18808-Ljbffr Parexel
- ...is seeking an experienced Clinical Research Associate to oversee site management and ensure regulatory compliance. The candidate will... ...informed consent processes, and maintain data integrity throughout the trial. A Bachelor's degree or RN and knowledge of Good Clinical...SeniorWebsiteFlexible hours
$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...SeniorWebsite- ...Clinical Trials Monitor The Clinical Trials Monitor helps to ensure compliance of the clinical... ...of remote data review and on site monitoring visits. Some travel will be required... ...and other issues is highly desirable Excellent communication skills Ability to work...WebsiteWork at officeLocal areaRemote work
- ...execution of a global clinical trial Responsible for... ...Form(s), eCRFs, monitoring conventions, edit checks... ...research staff, CRO, CRAs, sites and other contract... ...Sciences and 5+ years as a Senior Clinical Trial Manager... ...simultaneously. Excellent problem-solving, leadership...SeniorWebsiteContract work
- ...Senior Medical Director, Clinical Development (Medical Monitoring) About the Company Rapidly growing organization in the oncology... ...and interpretation of clinical trials. This includes serving as the... ...of contact for investigative sites and sponsors, and providing real...SeniorWebsite
- ...seeking a dynamic and experienced Senior Clinical Trial Manager. This role requires a... ...regulatory requirements. Support trial site selection, initiation, monitoring, and closure across multiple... ...effectively under tight timelines. Excellent organizational skills, with attention...SeniorWebsiteWork at office
- ...airport. Job Purpose: The Site and Monitoring Health Lead (SMH Lead) will... ...the quality of clinical trial execution at investigator sites... ...Proficient with MS Office Suite (Excel, Word, and PowerPoint); able... ...visits required Lead CRA experience required Experience...WebsiteLocal areaRemote work
$110k - $135k
...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 have over 3 years...WebsiteRemote job- ...effectively in an independent trial management role for at least a... ...documents, study reference documents, site materials, trainings and other... ...subject enrollment, clinical monitoring, site and vendor compliance... ...for potential gaps in site/CRA training, conducting co-...SeniorWebsiteContract workInterim role
- ...Senior Clinical Trial Manager At Verastem Oncology, we're advancing innovation... ..., and amendments for sites/vendors. Assist in developing... ...documents. Liaise with medical monitor and cross functional team... ...care field is required. Excellent understanding of ICH, GCP...SeniorWebsiteContract workLocal area
- Summary The Senior Clinical Trial Manager will lead the day-to-day activities... ...with clinical trial sites, and partner with key internal... ...can include onsite or remote monitoring, co‑monitoring, and training... ...company (Industry Sponsor). Excellent communication skills....SeniorWebsiteRemote work
$120k - $150k
...Centessa is seeking a Clinical Trial Manager (CTM) to lead the... ...close‑out, ensuring operational excellence, high data quality, and... ...clinical trials, including co‑monitoring activities, to ensure delivery... ...study milestones, including site activation, enrollment progress...SeniorWebsiteFull timeRemote work- ...Job Description SummaryThe Senior Clinical Trial Manager will lead the day-... ...collaboratively with clinical trial sites, and partner with key... ...include onsite or remote monitoring, co-monitoring, and... ...company (Industry Sponsor). ~ Excellent communication skills. ~ Extensive...SeniorWebsiteContract workRemote work
- ...CRA II, Permanent Full Time At Thermo Fisher Scientific, you'll discover meaningful... ...life changing therapies. With clinical trials conducted in 100+ countries and ongoing... ...different aspects of the clinical monitoring and site management process. This full-time home...SeniorWebsitePermanent employmentFull timeLive inRemote workWork from homeFlexible hours
$140k - $175k
...The Role We're looking for a Senior Clinical Trials Manager who will own the... ...manage third‑party clinical sites, write IRB and informed consent... ..., enrollment management, monitoring, and close‑out. Write and... ..., and CRO oversight. Excellent written and verbal communication...SeniorWebsiteFull timeContract workImmediate startWorldwideNight shift- Parexel is seeking a Senior Clinical Research Associate to be responsible for managing site monitoring and ensuring compliance with clinical trial standards. The role requires a minimum of 3 years of monitoring experience, preferably in Oncology, along with a relevant bachelor...SeniorWebsiteRemote jobLocal area
$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 PharmaceuticalsSeniorWebsiteHourly payContract work- We’re hiring a Senior Clinical Trials Manager to own the full lifecycle execution of clinical studies... ...between internal teams and external sites, investigators, IRBs, CROs, and vendors... ...selection, activation, enrollment, monitoring, and overall study management Author and...SeniorWebsite
$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...SeniorWebsite- ...Notice**Title:**Clinical Monitoring Lead**Company:**Ipsen... ...culture of collaboration, excellence and impact. At Ipsen,... ...CRO clinical and site management activities,... ...jeopardizing the start of a trial. + Support the Clinical... ...such as: - act as site CRA as directed by line manager...WebsiteContract workLocal area
- Senior/Clinical Trial Manager (CTM) - Mandarin Key Areas of Responsibilities... ...informed consent form, CRF, monitoring plans, regulatory... ...relationships with investigators and site staff Ensure audit‑ready... ...Myasthenia Gravis preferred Excellent communication, writing, and...SeniorWebsiteContract work
- Overview Senior Clinical Trial Manager (12 month contract) Reports to: Director... ...to CROs, other vendors, CRA team, and CTAs. Develop timelines... ...Plan, negotiate, and manage site budgets as well as... ...player Detail oriented with excellent organizational skills Ability...SeniorWebsiteContract workWork at officeRemote work3 days per week
- ...Parexel FSP is looking for a CRA/Sr CRA in the US.... ...the studies at allocated sites and is an active... ...the responsibility for monitoring the study conduct to ensure... ...Skills (Essential): Excellent attention to detail.... ...delivering quality clinical trials with reduced budget and...SeniorWebsiteLocal areaRemote workFlexible hoursShift work
$62.2k - $74.2k
The Clinical Trials Monitor ensures compliance of the clinical research enterprise with regulatory policies and guidelines. Under the direction... ..., responsible conduct of research, and other issues. Excellent communication skills. Ability to work with diverse constituencies...Work at officeLocal areaRemote work- ...for implementation of one or more clinical trials and all activities from study start-up... ...development, review, and operational aspects of site investigator grants and grant payment in... ...study related materials such as Clinical Monitoring Plans, Data Management Plans, eCRF forms...SeniorWebsiteContract workRemote work
$164k - $185k
...Sr. Clinical Trial Manager Cambridge, MA We are... ...experienced and driven Senior Clinical Trial Manager... ...protocol input, country and site selection, vendor... ...informed consent forms, monitoring plans, submission packages... ...-oriented mindset. Excellent interpersonal,...SeniorWebsiteFull time$87.2k - $169.3k
...IQVIA Biotech is seeking Sr. CRA 1 candidates with a minimum of 2 years of on-site monitoring experience in oncology. IQVIA Biotech is a full-service CRO purpose... ...) site documents are available for filing in the Trial Master File (TMF) and verify that the...SeniorWebsiteFull timePart timeLocal areaImmediate startWorldwide$140k - $155k
...motivated, and experienced Senior Clinical Trial Associate or Manager to drive... ...Investigator Brochure, Clinical Monitoring Plan, Project Plan. Assist... ...of the study including site activation, patient enrollment... ...skills including knowledge of Excel, Word, PowerPoint, Outlook...SeniorWebsiteInterim roleLocal area$90k - $110k
...epilepsy with additional clinical trials for neuropathic pain and... ...as we are! Your Impact As a Senior Clinical Trial Associate, you... ...protocol amendments, IBs, ICF's, monitoring visit reports, etc. Supports... ...including knowledge of Excel, Word, PowerPoint and Outlook...SeniorWebsiteFull timeContract workWork at officeLocal areaImmediate startFlexible hours$82.02k - $123.03k
Clinical Trial Associate / Sr. Clinical Trial Associate, Clinical... ...track record of executional excellence, combined with our depth of expertise... ...investigators, and clinical site staff to support study... ...GCP guidelines, clinical trial monitoring, and/or regulatory compliance...SeniorWebsiteTemporary workRemote workWork from homeFlexible hours3 days per week
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