Remote Clinical Research Associate (CRA) - Site Monitoring & Compliance
Merck
Boston, MA
- Remote job
Merck in the United States is seeking an experienced CRA Site Manager to oversee performance and compliance for assigned protocols and sites, ensuring adherence to ICH/GCP and local regulations. You will act as primary site contact, develop and expand site networks, support coordination with sponsors and internal stakeholders, and drive quality through documented visits and regulatory reviews. #J-18808-Ljbffr Merck
Vacancy posted 2 days ago
Similar jobs that could be interesting for youBased on the Remote Clinical Research Associate (CRA) - Site Monitoring & Compliance in Boston, MA vacancy
- Merck seeks a Clinical Research Associate to oversee performance and compliance for assigned protocols and sites in the United States. The role reports to the CRA-Manager and ensures adherence to ICH... ...relationships, conduct on-site and remote monitoring, and coordinate with...Remote workWebsiteLocal area
- ...Description C-Clinical is looking for an... ...Senior Clinical Research Associate to support clinical... ...investigative sites while maintaining... ...includes both remote monitoring and on-site visits... ...to protocol compliance and data integrity... ...you are a Senior CRA based in the greater...Remote workWebsite
Myana
San Diego, CA3 days ago - ...Clinical Research Associate CRA The Clinical Research Associate will... ...by ensuring quality, compliance, and operational excellence... ...across study sites. This position involves independent monitoring activities, site relationship... ...monitoring visits remotely and onsite while...Remote workWebsiteInterim roleFlexible hours
Jobgether
United States2 days ago - ...Summary Experienced Clinical Research Associate (CRA) - join our growing team... ...submission and approval of monitoring visit reports; ~... ...closeout visits at research sites in compliance with the approved protocol... ...On-site and virtual/remote monitoring activities with...Remote workWebsiteContract workWork at officeLocal areaImmediate startWork from homeHome officeFlexible hours
Medpace
United States3 days ago $108.5k - $201.5k
...Summary This is a remote position where... ...Florida. The Senior CRA performs monitoring activities... ...Phase I-IV Pharma clinical trials within the... ...Serves as the primary site manager for assigned... ...to ensure compliance with protocol, GCP... ...specifically clinical trial/research Knowledge of...Remote workWebsiteLocal areaRelocationNovartis Group Companies
East Hanover, NJ1 day ago- Merck is seeking a Clinical Research Associate to manage site performance and compliance within protocols across the U.S. This role involves significant travel of approximately 65-75% and requires strong relationships with research sites to ensure successful trial execution...Remote jobWebsite
- Merck & Co. is seeking a Clinical Research Associate to oversee performance and compliance for assigned sites and protocols in South Florida... ...covers site management, monitoring, regulatory documentation,... ...relationships, performing on-site and remote monitoring, coordinating...Remote jobWebsite
- Merck is seeking an experienced Clinical Research Associate/Monitor to ensure performance and compliance for assigned protocols and sites. You will act as the primary site contact, develop new sites, and manage monitoring activities across all trial phases. The role requires...Remote jobWebsite
- Merck is seeking a Clinical Research Associate to oversee site management for US-based clinical trials, ensuring compliance with ICH-GCP, regulatory standards... ...English, possess robust monitoring skills, and travel about 65-75% while working remotely as part of a global team...Remote jobWebsite
- Merck in the United States seeks a Clinical Site Manager/Monitor to ensure compliance with ICH-GCP and country regulations across assigned sites, with emphasis... ...with sponsor teams, performing on-site and remote monitoring, and driving site readiness through start-...Remote jobWebsite
- Merck & Co. is seeking a Clinical Research Associate to manage study sites across protocols, ensuring ICH-GCP compliance and regulatory readiness. The role involves on-site and remote monitoring, site initiation, and data integrity oversight across multiple regions. Ideal...Remote workWebsite
- Merck is seeking a Clinical Research Associate to oversee performance and compliance for assigned sites across a country, with remote and on-site monitoring. You will manage sites, drive recruitment, and ensure regulatory documentation and quality standards are met worldwide...Remote jobWebsiteWorldwideFlexible hours
$66.8k - $125k
...Clinical Research Associate (Level II) Join us as a Clinical Research Associate... ...aspects of the clinical monitoring and site management process. As a... ...II), you'll conduct remote or on-site visits to assess... ...protocol and regulatory compliance and manage required documentation...Remote workWebsiteTemporary workWork at officeHome officeFlexible hoursNight shift- ...Parexel is seeking a Clinical Research Associate (CRA) based in Cheyenne, Wyoming, responsible for managing clinical study sites and ensuring compliance with regulations. The CRA will collaborate... ...study team, train site staff, and monitor study conduct. The ideal...WebsiteLocal area
PAREXEL
Cheyenne, WY4 days ago - ...Parexel is looking for a Clinical Research Associate (CRA) in Annapolis, Maryland, to manage clinical studies at allocated sites. The CRA will ensure study commitments are achieved timely and in compliance with guidelines. The ideal candidate must have a Bachelor’s degree...Website
PAREXEL
Maryland3 days ago - ...Parexel is seeking a Clinical Research Associate in Providence, Rhode Island. The CRA will manage clinical studies at local sites, ensuring compliance with ICH-GCP and local regulations. Responsibilities... ...include training site staff, monitoring study progress, and conducting...WebsiteLocal area
PAREXEL
Providence, RI3 days ago $85k - $125k
Remote Jobs is looking for a Clinical Research Associate (CRA) to join their team in the United States. The CRA will be responsible for site monitoring, ensuring compliance with protocols, and providing leadership in clinical trial management. This role requires a strong...Remote jobWebsite- ...Companies is seeking a Clinical Research Associate (CRA) to support oncology... ...for an experienced monitor with a strong... ...in oncology studies, site management, and ensuring... ...regulatory and protocol compliance across multi-site... ...This role is fully remote for candidates located...Remote workWebsite
Piper Companies
New York, NY4 days ago - ...Precision Medicine Group is seeking a CRA II with experience in monitoring and site management. This remote role requires residency in Texas or California and involves overseeing clinical research studies, ensuring high-quality data, and managing site start-up procedures...Remote workWebsite
Precision for Medicine
Dallas, TX3 days ago - Merck & Co. is seeking a Clinical Research Associate Manager responsible for performance and compliance of sites across multiple protocols. The role reports to the CRA‑Manager and ensures study conduct... ...develop and expand the territory, monitor sites, and coordinate with...Remote jobWebsite
- ...Clinical Research Monitor Job ID: 26374 Location: Remote (Preferred Central U.S.) Duration: 24 Months... ...years Clinical Research/CRA monitoring experience... ...ISO 14155 ~ GCP/SOP compliance Experience with... ...Monitor clinical trial sites and ensure protocol/GCP...Remote workWebsite
Artech
United States1 day ago - ...Parexel is seeking a Senior Clinical Research Associate (Sr. CRA) in Pierre, South Dakota. The Sr. CRA will manage site monitoring for clinical trials, ensuring compliance with Good Clinical Practices and regulatory standards. This role requires a bachelor's degree in...Remote workWebsite
PAREXEL
Pierre, SD3 days ago - A leading clinical research company is seeking a Lead Clinical Research Associate (CRA) to manage full site monitoring services. The ideal candidate must be fluent in English and French... ...project site budgets, and ensuring compliance with regulatory guidelines. The position...Remote workWebsiteWork from home
Medium
Ottawa, IL4 days ago $85k - $104k
AtriCure, Inc. is seeking a Clinical Research Associate II to manage clinical investigation sites effectively. The CRA II will ensure compliance with protocols while collaborating closely... ...Responsibilities include site training, monitoring, and reporting. The position offers...Website- ...Parexel is hiring a Senior Clinical Research Associate in Baton Rouge, Louisiana. The Sr. CRA oversees site management and monitoring for clinical trials, ensuring compliance with GCP and FDA regulations. Candidates must have a Bachelor's in life sciences and a minimum...Remote workWebsiteLocal area
PAREXEL
Baton Rouge, LA3 days ago $65 - $90 per hour
...C-Clinical is seeking a Senior Clinical Research Associate to support clinical trials... ...professional who enjoys site interaction,... ...combines remote... ...routine on-site monitoring visits, allowing... ...and protocol compliance throughout the... ...are a Senior CRA located in the...Remote workWebsiteHourly payC-Clinical
Doral, FL3 days ago$85k - $120k
...seeking an Oncology Clinical Research Associate to support a... ...managing investigative sites and ensuring the... ...and regulatory compliance.... ...Perform site monitoring activities through both remote evaluations and on... ...Research Associate, CRA, Clinical Trials,...Remote workWebsitePiper Companies
Chicago, IL3 days ago- ...Clinical Research Associate II (CRA II) Oncologist As a Clinical Research Associate... ...feasibility assessments, and site selection processes... ...manuals Clinical Trial Monitoring: Conduct site... ...close-out visits to ensure compliance with the study protocol,...Remote workWebsiteInterim roleLive in
Perspective Therapeutics, Inc.
United States3 days ago $50 - $62 per hour
...currently seeking a Clinical Research Associate III for a prominent... ...contact for assigned sites, providing direct oversight... ...Conduct on-site and remote monitoring activities for Phase... ...concerns, and compliance risks in a timely... ...or sponsor‑dedicated CRA role is preferred; candidates...Remote workWebsiteThe Fountain Group
Wausau, WI3 days ago- ...This remote role requires a resident of Texas or California. Position Summary The CRA II is a seasoned, experienced professional in monitoring and site management. Responsibilities will vary with the... ...implementation, on‑site monitoring of clinical research studies, and ongoing site...Remote workWebsiteContract workLocal areaNight shift
Precision for Medicine
Sacramento, CA4 days ago
Do you want to receive more vacancies?
Subscribe and receive similar vacancies to Remote Clinical Research Associate (CRA) - Site Monitoring & Compliance. Be the first to apply!
Related searches
- clinical research administrator Boston, MA
- clinical trials assistant Boston, MA
- clinical research assistant Boston, MA
- clinical research associate cra Boston, MA
- clinical research associate Boston, MA
- on-site clinical research associate (traveling/remote) Boston, MA
- community monitor Boston, MA
- clinical research monitor Boston, MA
- monitor Boston, MA
- security monitor Boston, MA