Sign up to access all features of our service.
  • Job search
  • Favorites
  • Create a CV
    New
  • Salaries
  • Subscriptions

Remote CRA: Site Monitoring & Compliance Expert

Merck

Raleigh, NC
  • Remote job

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. The role requires 5+ years in healthcare with direct site management experience in bio/pharma/CRO, and travel up to 75% with a valid driver’s license. Flexible remote work arrangements are available. #J-18808-Ljbffr Merck

Vacancy posted 3 days ago
Similar jobs that could be interesting for youBased on the Remote CRA: Site Monitoring & Compliance Expert in Raleigh, NC vacancy
  •  ...Associate to oversee performance and regulatory compliance for assigned sites across the country, under the CRA-Manager. You will ensure study conduct aligns with...  .... The role requires strong site management, monitoring expertise, and collaboration with cross-functional... 
    Remote job
    Website

    Merck & Co.

    New York, NY
    1 day ago
  •  ...experienced Clinical Research Associate to oversee site performance across trials, ensuring ICH-GCP compliance and regulatory alignment. The role acts as primary...  ...sponsors and investigators. Travel up to 75% and remote work options are available; requires strong clinical... 
    Remote job
    Website

    Merck & Co.

    Rahway, NJ
    2 days ago
  • 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... 
    Remote job
    Website
    Local area

    Merck

    Boston, MA
    2 days ago
  • 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 job
    Website

    Merck

    Sacramento, CA
    2 days ago
  •  ...Clinical Research Associate to oversee performance and compliance for assigned protocols and sites across multiple locations in the United States. You...  ...requires developing site relationships, coordinating monitoring activities, and supporting site selection with extensive... 
    Remote job
    Website

    Merck & Co.

    Annapolis, MD
    1 day ago
  • 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 work
    Website

    Merck & Co.

    Rahway, NJ
    2 days ago
  • Syneos Health is seeking a Clinical Research Associate II (CRA II) in the United States. In this role, you will perform site qualifications, manage monitoring activities, and ensure protocol compliance. You will leverage your expertise to assess site performance and protect... 
    Website

    Syneos Health

    New York, NY
    2 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 work
    Website

    Precision for Medicine

    Dallas, TX
    3 days ago
  •  ...Clinical Research Monitor Job ID: 26374 Location: Remote (Preferred Central U.S.) Duration...  ...years Clinical Research/CRA monitoring experience ~...  ...~ ISO 14155 ~ GCP/SOP compliance Experience with:...  ...Monitor clinical trial sites and ensure protocol/GCP/regulatory... 
    Remote work
    Website

    Artech

    United States
    1 day 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 type and timing of the program to which the CRA II is assigned and typically... 
    Remote work
    Website
    Contract work
    Local area
    Night shift

    Precision for Medicine

    Sacramento, CA
    4 days ago
  • Optimapharm, a global CRO, is seeking a Senior CRA for the US Clinical Operations team. This remote role supports oncology studies across sites, applying ICH GCP standards and driving site initiation, monitoring, and closeout visits. You will mentor colleagues, manage... 
    Remote job
    Website

    Optimapharm

    Raleigh, NC
    4 days ago
  • A leading clinical research organization is seeking a Clinical Research Associate (CRA) in Atlanta, Georgia to manage clinical study sites. This role involves monitoring compliance with international guidelines, supporting investigators, and ensuring timely study delivery... 
    Remote job
    Website

    Parexel

    Atlanta, GA
    1 day ago
  •  ...& Co., Inc. is seeking an experienced CRA-Manager level professional to ensure performance and compliance for assigned protocols and sites. The role oversees study conduct to ICH...  ...research, participate in planning and monitoring activities, and collaborate with global... 
    Remote job
    Website

    Merck

    Boston, MA
    2 days ago
  • $115k - $125k

    A leading clinical research organization is seeking a Clinical Research Associate (CRA) for a remote permanent position based out of CST. The CRA will conduct site monitoring visits, support subject recruitment, and manage communication with study sites. Candidates should... 
    Remote job
    Website
    Permanent employment

    Piper Companies

    New York, NY
    2 days ago
  • $105k - $125k

     ...Responsible for all aspects of study site monitoring including routine monitoring and close-out...  ...experience ~ Ophthalmology experience as a CRA ~ Open to various hub locations...  ...attendance. Varied hours may be required. - Remote Applications will be accepted on an... 
    Remote work
    Website
    Full time
    Part time
    Work at office
    Local area
    Flexible hours

    Fortrea

    Florida, NY
    4 days ago
  • Merck seeks an experienced CRA to manage and monitor clinical study sites, ensuring adherence to ICH-GCP and country regulations. The role acts as primary contact for sites, develops relationships, and drives site readiness across all trial phases. You will travel up to... 
    Remote job
    Website

    Merck

    Columbus, OH
    4 days ago
  • Merck is seeking a CRA manager/outcome oriented professional to oversee site performance and study conduct across multiple...  ...The role demands ensuring ICH/GCP compliance, managing site relationships,...  ...internationally (about 75%) and may work remotely. A relevant healthcare... 
    Remote job
    Website
    Relocation

    Merck

    Atlanta, GA
    2 days ago
  •  ...IQVIA is seeking a Clinical Research Associate (CRA) to advance clinical research. In this role, you will lead site monitoring visits and ensure study execution compliance and data integrity. Ideal candidates have a Bachelor's degree in life sciences and at least 1.5 years... 
    Website

    IQVIA

    Durham, NC
    4 days ago
  •  ...IQVIA is seeking a Clinical Research Associate (CRA) in Glendale, Arizona. The candidate will lead site monitoring visits to ensure high-quality clinical trials, build...  ...with investigative sites, and maintain compliance with GCP and ICH guidelines. The ideal candidate... 
    Website

    IQVIA

    Glendale, CA
    3 days ago
  •  ...IQVIA in Columbia, Maryland is looking for a Clinical Research Associate (CRA) to lead clinical trials and ensure compliance and data quality. This role involves monitoring site visits, building relationships with investigative teams, and managing study progress. The ideal... 
    Website

    IQVIA

    Columbia, MD
    16 hours ago
  •  ...IQVIA LLC is seeking a Clinical Research Associate (CRA) to advance clinical research and patient outcomes. This role involves leading site monitoring visits, ensuring compliance, and managing study progress. You will collaborate with cross-functional teams and build... 
    Website

    IQVIA

    Durham, NC
    3 days ago
  •  ...IQVIA is looking for a Clinical Research Associate (CRA) in Carlsbad, California, to lead various clinical trials and ensure high-quality study execution. The successful candidate will monitor sites, manage study progress, and will have a significant impact on improving... 
    Website

    IQVIA

    Carlsbad, CA
    4 days ago
  • Merck is seeking a Senior CRA - Site Management to oversee monitoring and compliance for assigned sites across multiple trials. You will ensure data integrity, patient safety, and regulatory adherence while coordinating with cross-functional teams. The role requires travel... 
    Website

    Merck

    Denver, CO
    2 days ago
  •  ...IQVIA is seeking a Clinical Research Associate (CRA) in Rockville, MD to enhance clinical trial quality. The CRA will lead site monitoring visits, ensuring compliance and building relationships with sites for effective study delivery. Ideal candidates hold a Bachelor’... 
    Website

    IQVIA

    Rockville, MD
    16 hours ago
  • Consultant, CRA / Clinical Monitor - Medical Device (Oncology) Galveston, TX (Onsite...  ...subject safety, regulatory compliance, and high‑quality data...  ...a small pilot study (single site). This individual will work...  ...closeout visits (onsite and/or remote as appropriate) Ensure... 
    Remote work
    Website
    Contract work
    Interim role
    Immediate start

    Confidential

    Galveston, TX
    2 days ago
  •  ...passionate Clinical Research Associate (CRA) in Phoenix, Arizona. You will play...  ..., collaborating with investigative sites and cross-functional teams to ensure study excellence and compliance. In this role, you will lead site monitoring visits, drive performance, and... 
    Website

    IQVIA

    Phoenix, AZ
    2 days ago
  •  ...Sacramento is seeking a Clinical Research Associate (CRA) to join their team in advancing clinical research and...  ...improving patient outcomes. This role involves leading site monitoring visits and ensuring compliance with regulatory standards. The ideal candidate will have... 
    Website

    IQVIA

    Sacramento, CA
    2 days ago
  •  ...IQVIA is seeking a Clinical Research Associate (CRA) in Annapolis, Maryland, to drive high-quality clinical trials. You will lead site monitoring visits, ensuring compliance and fostering strong relationships with investigative sites. The ideal candidate has a bachelor... 
    Website

    IQVIA

    Maryland
    4 days ago
  •  ...Research Associate to oversee performance and compliance for assigned study protocols across sites in the United States. The role reports to the CRA-Manager and ensures adherence to ICH/...  ...include site management, monitoring visits, regulatory documentation, and cross... 
    Website
    Local area

    Merck & Co.

    Saint Louis, MO
    1 day ago
  •  ...Clinical Research Associate II or Senior CRA to monitor and manage sites in accordance with ICH/GCP and FDA guidelines. This remote role is located within a 1-hour commute of...  ...assist site selection, ensure regulatory compliance, and support data integrity across multiple... 
    Remote job
    Website

    Remote Jobs

    New York, NY
    3 days ago

Do you want to receive more vacancies?

Subscribe and receive similar vacancies to Remote CRA: Site Monitoring & Compliance Expert. Be the first to apply!