Remote Clinical Research Associate: Regulatory & Trials
Biopharmaceutical Research Company
Biopharmaceutical Research Company is seeking a detail-oriented Research Associate for a remote position focused on clinical and nonclinical research. The ideal candidate will have a Master’s degree in a life sciences discipline and at least two years of relevant experience in supporting clinical trials. Responsibilities include study planning, reviewing documentation, and conducting literature reviews. The role offers competitive benefits, including 401(k) matching and health insurance. #J-18808-Ljbffr
- ...company is looking for a Senior Clinical Research Associate to oversee clinical trials in the United States. The position... ...including site management, regulatory compliance, and data quality assurance... ...sites effectively. This remote role offers an opportunity to significantly...Remote workRegulatory
$89k - $148k
Itlearn360 is seeking a Clinical Research Associate to lead innovative clinical trials. The successful candidate will be responsible for ensuring compliance during site visits, contributing to regulatory documentation, and managing site relationships. Ideal candidates should...Remote jobRegulatoryFlexible hours$103k - $130k
...Business Community is seeking a Sr. Clinical Research Associate to manage setup, execution, and monitoring of clinical trials for IVD and medical devices. This remote position requires substantial... ...experience and knowledge of regulatory standards. The role involves oversight...Remote jobRegulatory- ...Clinical Research Associate/Clinical Trial Monitor Frederick, Maryland Frederick, Maryland has a little bit... ...ORA is a multidisciplinary team of regulatory affairs, compliance, and clinical... ...monitoring activities to include remote review of electronic source documents...Remote workRegulatoryContract workWork at office
$66.8k - $120k
...Job Description Join Us as a Clinical Research Associate (Level II) - Make an Impact at... ..., spanning 2,700 clinical trials across 100+ countries in the... ...Associate (Level II), you'll conduct remote or on-site visits to assess protocol and regulatory compliance and manage...Remote workRegulatoryTemporary workWork at officeHome officeFlexible hoursNight shift- ...A leading medical technology company is seeking a Remote Regional Clinical Research Associate II. This role involves conducting monitoring visits and ensuring compliance with regulatory standards. Ideal candidates have a Bachelor's degree in nursing or a life science,...Remote workRegulatoryWork from home
$50 - $60 per hour
...and highly motivated Contract Clinical Trial Assistant of Clinical... ...and CRA training material, regulatory documents, lab and pharmacy... ...directly with sites, Contract Research Organizations (CROs), vendors... ...CTA: 3 years (Required) Work Location Remote #J-18808-Ljbffr...Remote workRegulatoryHourly payContract work$110k - $125k
Paragonix Technologies, Inc. is looking for a Senior Clinical Research Associate in Boston, MA, to oversee randomized clinical studies focusing... ..., clinical operations, and ensuring compliance with regulatory standards. The candidate should have at least 6 years of...Remote jobRegulatory- We are seeking a Clinical Trial Administrator to provide high-quality comprehensive... ...within the EMS Community Research Units ensuring study... ...of organisation,accuracyand regulatory compliance. The post holder... ...related meetings. Remote Community Site Support Provide...Remote workRegulatoryWork at officeNight shift
- ...A leading CRO firm seeks a Clinical Research Associate to monitor clinical trials, ensuring compliance with regulatory standards. The candidate must possess a Bachelor's degree... ...recruitment and data integrity. Opportunities for remote work and active involvement in ophthalmic...Remote workRegulatory
- ...Orca Bio is seeking a Clinical Research Associate to monitor the progress of clinical... ...studies, either on-site or remotely. The ideal candidate will have... ...visits, managing clinical trial documentation, and ensuring compliance with regulatory standards. Benefits include...Remote workRegulatory
- ...A biopharmaceutical company is seeking a dynamic Clinical Research Associate to manage and monitor clinical trial sites. This remote role involves ensuring compliance with study protocols and regulatory requirements. The ideal candidate will have a Bachelor's degree in...Remote workRegulatory
$120k - $135k
...Companies is actively seeking Clinical Research Associates to join a highly... ...CRO. This position is fully remote but does require travel 6... ...execution of the clinical trial plans and protocols for Phase... ...Experience with the FDA or similar Regulatory and Accrediting...Remote workRegulatory- ...Senior Clinical Research Associate - IC Preferred- Texas Direct message the job poster... ...programs, ensuring the trial is conducted in compliance... ...protocol, ICH/GCP, applicable regulatory requirements and applicable... .... This role is fully remote, with approximately 70% travel...Remote workRegulatory
$63.25k - $102.6k
...coordination of CTNI-managed clinical trials. Competencies Required... ...to introduce innovations to research study Ability to prepare/monitor... ...of data Assists with study regulatory submissions Verifies... ...appropriate Employment Details Remote Type: Hybrid Work Location:...Remote workRegulatoryWork experience placementMonday to FridayShift work- ...Senior Clinical Research Associate job at PSI CRO. Remote. We are the company that cares – for our staff, for our clients... ...in feasibility research Support regulatory team in preparing documents for... ...monitoring complex Oncology trials required; experience with radiopharmaceuticals...Remote workRegulatoryWork from homeWork visa
- ...CLINICAL RESEARCH ASSOCIATE PURPOSE This role supports breast and colorectal cancer clinical trial operations and the primary deliverables of ensuring... ..., data integrity and regulatory compliance. The... ...and Thursday) and 2 days remote work (Wednesday and Friday...Remote workRegulatoryInterim roleWork at office
- ...Position: Senior Clinical Research Associate (level dependent on experience) Location... ..., and especially with our remote employees, is incredibly... ...investigational product(s) and trial-related material. Maintains... ...document review (SCV), regulatory documents, and investigational...Remote workRegulatoryLocal areaWork from homeHome office
$78k - $130k
...Positions available: 1 (remote based, Canada) Must be fluent in... ...deliver and/or perform full clinical site monitoring services for... ...monitoring project site budgets and regulatory filings that aligns with SOPs... ...the movement and delivery of trial materials, samples, tests and...Remote workRegulatoryWork from home$100k - $110k
...Piper Companies is seeking a Clinical Research Associate II to join a global... ...life sciences industry for a remote permanent role with 60-75%... ...sites to ensure high-quality trial execution. Responsibilities... ...source documentation, and regulatory files to confirm accuracy,...Remote workRegulatoryPermanent employment$115k - $125k
...Piper Companies is seeking a Clinical Research Associate (CRA) to join a global... ...healthcare analysis for a remote permanent position located... ...for monitoring and clinical trials across the region for a leading... ...compliance with GCP, ICH, and regulatory guidelines. Support subject...Remote workRegulatoryPermanent employmentWork at office- ...Senior Clinical Research Associate (US) Remote Position Summary The Sr. CRA is responsible for the oversight and monitoring clinical trials to ensure they are conducted in compliance with the study... ...with protocol, ICH-GCP, and regulatory requirements Oversee review and...Remote workRegulatoryInterim role
- ...Bonus and RSUsSite Director, Clinical Operations (CRA) - Midwest RegionRemote... ...readiness, and local regulatory and IRB/EC submissions for... ...site activities both onsite and remotely, ensuring patient rights,... ...contract negotiations for clinical trial agreements, collaborating...Remote workRegulatoryContract workLocal area
- Senior Clinical Research Associate, Psychiatry - Southeast - Remote page is loaded## Senior Clinical Research Associate, Psychiatry... ....We are Worldwide Clinical Trials, and we are a global team of... ...extensive support through regulatory submissions, TMF management, and...Remote workRegulatoryWork at officeWorldwide
$70k - $115k
...Clinical Research Associate The Clinical Research Associate (CRA) is primarily... ...the rights and wellbeing of trial participants are protected... ...guidelines, local and global regulatory requirements, and Novotech/... ...conducted either onsite or remote as per CMP. Ensure the...Remote workRegulatoryLocal areaFlexible hours- ...Description/Comment: The Clinical Research Associate (CRA) for Beckman Coulter Diagnostics... ...business unit and is fully remote. You will report... .../worksheets) and ensure Trial Master File (TMF), Sponsor... ...to Protocol, applicable regulatory standards, IRB policies and...Remote workRegulatoryContract workWork experience placementWork at office
- ...focused on cervical spine conditions is seeking a Clinical Research Associate. Responsibilities include managing clinical trials, ensuring compliance, and coordinating... ...the medical device field. This role allows for remote work and offers opportunities to innovate traditional...Remote work
$120k - $140k
...- $140,000.00/yr Job Details Remote Senior CRA position in the oncology... ...through all phases of the trial. Conducts site visits... ...reviews, and monitors required regulatory documents for study start‑up,... ...management. Works with in‑house Clinical Trial Assistant to collect, review...Remote workRegulatoryInterim roleLocal areaFlexible hours$20.16 - $29.01 per hour
...nurses, business people, tech experts, researchers, and systems analysts to advance... ...general supervision to ensure the regulatory requirements for clinical trials are met. This position involves... ...Additional Job Details (if applicable) Remote Type Hybrid Work Location...Remote workRegulatoryHourly payContract work- ...Summary In this Clinical Research Associate role (may be contract or full‑time employee), you... ...at investigative sites or remotely, and ensure clinical trials are conducted, recorded, and reported... ...SOPs), ICH‑GCP, and all applicable regulatory requirements. You can be based...Remote workRegulatoryFull timeContract workInterim roleLocal area
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