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
- ...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
$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- ...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
$120k - $140k
Remote Senior Clinical Research Associate (CRA) - Oncology Salary: $120,000 - $140,000 per year... ...strong investigative site relationships and ensures... ...through all phases of the trial. Conducts site visits including... ...visits, interim monitoring visits, and close‑out visits...SeniorWebsiteRemote jobInterim roleLocal areaFlexible hours- ...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...SeniorWebsite
- 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
- ...Senior Clinical Trial Manager The Senior Clinical Trial Manager will lead... ...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
$140k - $175k
...Role We're looking for a Senior Clinical Trials Manager who will own the end... ...third-party clinical sites, write IRB and informed consent... ...activation, enrollment management, monitoring, and close-out. Write... ..., and CRO oversight . ~ Excellent written and verbal...SeniorWebsiteFull timeContract workImmediate startWorldwideNight shift$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$90k - $180k
...subject-matter expertise. We are currently seeking a Senior Guideline Monitoring Analyst (“Analyst”) who will be part of the Investment Operations... ...both independently and collaboratively ~ Possess excellent attention to detail ~ Exhibit strong proficiency in...SeniorWebsiteRemote workFlexible hours1 day per week$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- 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
$74.9k - $82.4k
The Clinical Trials Monitor helps to ensure compliance of the clinical research enterprise with all related regulatory policies and guidelines... ...interest, responsible conduct of research, and other issues Excellent communication skills Ability to work with diverse...Work at officeLocal areaRemote work- ...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
- ...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- ...Clinical Trial Manager Acrivon is a clinical stage biopharmaceutical... ...with investigator sites, vendors, cross-functional colleagues... ...subject enrollment, clinical monitoring, compliance at clinical sites,... ...Project, Word, PowerPoint, and Excel Proven ability to multi-task...SeniorWebsiteContract workLocal area
$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- ...design, generating clinical documents, monitoring ongoing studies, and reporting findings.... ...attention to detail, multi-tasking ability, and excellent communication skills are essential. This... ...to contribute significantly to clinical trials and their compliance. #J-18808-Ljbffr...Website
- ARTBIO is seeking a Senior Clinical Trial Manager to oversee the daily operations of clinical trials in Cambridge... ...cross-functional teams, managing clinical sites, and ensuring compliance with GCP, ICH, and FDA regulations. Excellent communication and leadership skills are...SeniorWebsite
$160k - $200k
Senior Manager, Patient Support Operations Sana... ..."Patient and Site Navigator" for our... ...management of clinical trials in accordance with... ...therapy procedures; monitor ongoing operational... ...scientific rigor and excellent problem‑solving... ...research associate (CRA) with experience in...SeniorWebsiteTemporary workImmediate startRemote work- ...JOB TITLE: Senior Manager, Investigational Supply Operations... ..., inventory monitoring, and reconciliation for... ...interruptions to study sites. Manages external resources... ...Manuals for Clinical Trials. REQUIRED... ...Microsoft applications (Excel, Word, PowerPoint, Project...SeniorWebsiteRemote work
- ...Conduct site monitoring visits in accordance with standards of practice guidelines and federal regulations to ensure that the rights and well... ...at study initiation and as needed through the course of the trial -Review study-specific site documents, including regulatory...WebsiteWork at office
- ...Job Summary: The Senior Manager, Study Start-up partners... ...study start-up and site activation activities... ...world evidence clinical trials. This team member will... ...Manager, Study Start-up excels in project management,... ..., study management and monitoring, and local regulatory requirements...SeniorWebsiteLocal areaRemote work
$25 - $35 per hour
...nationwide. Based in Reno, NV, we have a 12-year track record of excellence and stability in the mortgage field services industry. We... ...are designed for speed, typically requiring only 5-6 minutes on-site. Consistency: Enjoy stable, month-to-month volume in your assigned...WebsiteHourly payPrice workExtra incomeFull timeFor contractorsFreelanceLive inFlexible hours- ...Position Overview The Senior Director, Quality Assurance... ...CROs, investigator sites, vendors, and internal... ...Support to Clinical Trial Teams Act as GCP quality... ...consent forms, monitoring plans, and data management... ...integrity, and operational excellence Qualifications and...SeniorWebsite
$141k - $188k
...Inc. is hiring a Sr. Manager - Clinical Trial Lead to manage clinical studies in Cambridge... ...study management, ensuring compliance, monitoring milestones, and engaging with cross-functional... ...experience in clinical operations and excels in project management. Biogen offers a...Senior
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