Remote Clinical Trial Associate - Startup & Regulatory
Allen Spolden
- Remote job
A clinical research organization is seeking a Remote Clinical Trial Associate to support operational strategy and execute clinical studies. Responsibilities include assisting with study startup, ensuring regulatory readiness, and collaborating with study teams and CROs. Candidates should have a Bachelor's degree and at least one year of experience in the pharmaceutical industry, along with strong task management and collaboration skills. Benefits include 401(k) with company match, health programs, and generous vacation policies. #J-18808-Ljbffr Allen Spolden
- ...Join Our Team at Worldwide Clinical Trials We're a global, midsize CRO that pushes boundaries, innovates and invents because the path... ...ensure data accuracy and integrity, crucial for groundbreaking regulatory submissions. With a variety of roles, from data support...Remote workRegulatoryWorldwide
- ...Job Opportunity The remote-based Clinical Trial Associate (CTA) will perform tasks related to supporting... ...clinical study activities, including regulatory inspection readiness, following... ...providing support to focus on study startup and site initiation activities, including...Remote workRegulatoryContract workNight shift
- ...Clinical Trial Associate Anywhere Type: Consulting Category: Clinical Ops Industry: Life Sciences Workplace Type: Remote Reference ID: JN -062026-107240 Date Posted: 06/02... ...in compliance with SOPs and regulatory guidelines. Maintain clinical...Remote workRegulatoryHourly payLocal areaShift work
- ...Clinical Trial Associate / Sr. Clinical Trial Associate, Clinical Operations At Agios, we are fueled... ..., including training records, regulatory packets, informed consent forms, site... ...This role has the ability to be either remote in the US or hybrid in our Cambridge...Remote workRegulatoryTemporary workWork from homeFlexible hours3 days per week
$100k - $135k
...Clinical Trial Management Associate San Francisco, CA or Remote or Hybrid Braveheart Bio is a Bay Area–based biopharmaceutical company pioneering best-in-class... ...study documents (e.g., informed consent forms, regulatory packages) and route for approval. Maintain...Remote workRegulatoryFlexible hours$82.02k - $123.03k
Clinical Trial Associate / Sr. Clinical Trial Associate, Clinical Operations Who we are: At Agios,... ...documentation, including training records, regulatory packets, informed consent forms, site... ...role has the ability to be either remote in the US or hybrid at our Cambridge...Remote workRegulatoryTemporary workWork from homeFlexible hours3 days per week$84.9k - $106.1k
...This position reports to the Associate Director, Clinical Data Management, Oncology... ...complete, and compliant clinical trial data. The Senior Clinical... ..., SOPs, and applicable regulatory requirements. Perform other... ...: Primarily remote role with periodic on-site...Remote workRegulatoryInterim roleWork at officeLocal areaFlexible hours$84.9k - $106.1k
...This position reports to the Associate Director, Clinical Data Management, Oncology... ...complete, and compliant clinical trial data. The Senior Clinical... ..., SOPs, and applicable regulatory requirements. Perform other... ...Requirements: Primarily remote role with periodic on-site...Remote workRegulatoryInterim roleWork at officeLocal areaWorldwideFlexible hours$48 - $55 per hour
Contract - Senior Clinical Trial Associate Cambridge, MA Title: Contract - Senior Clinical Trial Associate... ...Location: Cambridge, MA, Hybrid, or Remote Reports to: Head of Clinical... ...studies Track study status, enrollment, regulatory documentation, laboratory samples,...Remote workRegulatoryHourly payContract work$89k - $109k
...to learn more. JOB TITLE: Senior Clinical Quality Associate LOCATION: Remote - candidates based in the following... ...ensure adherence with applicable regulatory requirements and Aurion policies and... ...Company is preparing for clinical trials in the U.S. We are growing rapidly...Remote workRegulatoryFull timeDay shift$45k - $50k
...United States. Job Overview: The Clinical Trial Administrator (CTA) is an... ...by protocols, SOPs and regulatory standards, to ensure timely... ...sciences or related field; or Associates degree in the life sciences... ...Pay Range: $45-50k USD #LI - Remote Applications will be accepted...Remote workRegulatoryFull timeWork at officeLocal areaWorldwide- Optimapharm is hiring a Regulatory and Startup Specialist to support global clinical trials. This role involves leading regulatory submissions and coordinating study start-up activities. Suitable candidates should possess a degree in life sciences and have at least 4 years...Remote jobRegulatoryFlexible hours
- ...community physicians to offer clinical trials as a therapeutic option for... ...handle all infrastructure, regulatory compliance, and administrative... ...life science industry OR Associate’s degree with 2 years of relevant... ...is primarily performed in a remote/office environment and...Remote workRegulatoryWork at office
- ...Medical Monitor Associate Reporting to the Manager, Medical Monitoring, Medical Affairs... ...tasks related to medical oversight in clinical trials. This role will be perfect for you... ...by the Director, Scientific and Regulatory Affairs. Maintain up to date study...Remote workRegulatoryPermanent employmentFull timeWork from homeFlexible hoursShift work
- ...Through our PPD® clinical research services,... ...support clinical trials in more than 100 countries... ...and deliver startup activities for the... ...Clinical Research Associates with 2+ years of independent... ...(on-site and remote) using a risk-... ..., ICH-GCP, regulatory, and SOP compliance...Remote workRegulatoryPermanent employmentFull timeContract workWork at officeLocal areaWork from homeFlexible hours
- ...precision medicine. About Trial Library Trial Library,... .... is a venture-backed startup founded in 2022 focused... ...and retention to clinical trials with an AI-platform... ...inclusive. As a Clinical Associate Project Manager, you... ...Library Platform. This is a remote position. You will...Remote workFull time
$60k - $70k
...Coordinator Circuit Clinical® is on a mission to... ...the historical clinical trial methodologies through... ...team! As an emerging startup in Buffalo, where New... ...023 while growing our remote research capabilities... ...Clinical Operations, Regulatory, and Business Development...Remote workRegulatoryFull timeContract workLive inWork at officeShift work$80.17k - $109.47k
...Cancer Consortium Clinical Trial Startup Manager Fred Hutchinson Cancer Center is an independent... ...work closely with internal and external regulatory and fiscal specialists to manage start... ...and demonstrate accountability in a remote setting. PREFERRED QUALIFICATIONS...Remote workRegulatoryContract workH1bWork at officeVisa sponsorshipFlexible hours$90k - $130k
...is available for remote work in the following... ..., WA Vanguard Clinical, Inc. is a... ...innovation to clinical trial execution through... ...Management and Study Startup. As a small company... ...Clinical Research Associate (CRA) will execute... ...and applicable regulatory requirements. Solid...Remote workRegulatoryPermanent employmentFull timeContract workInterim roleWork at officeFlexible hours$204k - $306k
...General Summary: The Clinical Development Associate Medical Director will serve... ...Medical Lead for clinical trials, working with cross-... ...Participates in the preparation of regulatory documents in support of... ...as: 1. Hybrid : work remotely up to two days per week;...Remote workRegulatorySummer workFlexible hours2 days per week$240k - $360k
...Clinical Development Medical Director The Clinical Development... ...Medical Lead for Vertex clinical trials, working with cross-... ...Participates in the preparation of regulatory documents in support of regulatory... ...as: 1. Hybrid: work remotely up to two days per week; or select...Remote workRegulatorySummer workFlexible hours2 days per week$85k - $95k
...Vanguard Clinical, Inc. is a Contract Research Organization... ...to clinical trial execution through passion... ...Management and Study Startup. As a small company, we... ...the Clinical Operations Associate by taking on greater... ...with IRB/EC submissions, regulatory queries, and document...Remote workRegulatoryContract workWork at officeFlexible hours- ...NucS AI is a pioneering MedTech startup focused on transforming... ...patient outcomes and streamline clinical workflows. We collaborate with... ...studies, publications, or regulatory documentation Perform reviews... ...-time, contract, and fully remote with flexible hours (location...Remote workRegulatoryContract workPart timeFlexible hours
$17.74 - $29.55 per hour
...delivers the latest therapies, access to 300+ clinical trials, and state-of-the-art diagnostics-all... ..., and checklists according to all regulatory agencies. Will follow the AON patient... ...limited supervision. Ability to work remotely effectively as required. Must be...Remote workRegulatoryMonday to FridayShift workWeekend workAfternoon shift- A global biopharmaceutical leader is seeking an Associate Director Regulatory Affairs - Clinical Lead to enhance their regulatory team in EU. In this pivotal role, you will manage the EU regulatory strategy for innovative oncology programs within a dynamic and collaborative...Remote jobRegulatory
- EMS Healthcare in Chester, NY, is seeking a Clinical Trial Administrator to provide comprehensive administrative and operational support... ...maintaining high standards of study documentation, ensuring regulatory compliance, and supporting efficient trial conduct across multiple...Remote jobRegulatoryWork at officeFlexible hours
- ...Responsibilities: Excellent employment opportunity for a Clinical Trials Management Associate - II in the Foster City, CA area. Manages assigned... ...Assures site compliance with the routine protocol and regulatory requirements and quality of data. Assists in CRO...RegulatoryContract workInterim role
- ...About the job Clinical Diagnostics Associate Clinical Diagnostics Associate The Clinical Diagnostics... ...of quality, ethical, and regulatory standards, including ICH/GDPR/GCP/GLP... ...development, diagnostics, or clinical trial management. • Experience with Microsoft...RegulatoryWork experience placementWork at officeImmediate start
- ...Clinical Records Associate Maintain a minimal understanding of GCP, ICH and GLP regulations associated... ...and retention of clinical trial documentation and preclinical study records... ...May provide support during TMF-related regulatory agency and internal GCP inspections...Regulatory
$97.82k - $146.68k
Sitcancer is seeking a Clinical Research Monitor II to oversee the quality and regulatory compliance of oncology clinical trials. This role involves conducting remote monitoring activities, collaborating with various stakeholders, and ensuring adherence to regulatory standards...Remote workRegulatory
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