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Contract Research Ethics Jobs (NOW HIRING)

Winaxis

Clinical Research Coordinator

Boston, MA · On-site

$26.25 - $35/hr

Coordinate with Principal Investigators, sponsors, Contract Research Organizations (CROs ... Strong understanding of clinical trial processes and research ethics. Knowledge of ICH-GCP ...

Winaxis

Clinical Research Coordinator

Boston, MA · On-site

$26.25 - $35/hr

Coordinate with Principal Investigators, sponsors, Contract Research Organizations (CROs ... Strong understanding of clinical trial processes and research ethics. Knowledge of ICH-GCP ...

Houston Methodist

At Houston Methodist, the Research Contract Analyst position is responsible for various duties ... ethics * Exhibits a comprehensive understanding of HM interests regarding specific agreements

New

Central Coast Local Health District

... contract of employment will cease with two weeks notice. Maternity relief positions can be for a ... Liaise with Human Research Ethics Committees, research offices, government agencies and external ...

Justworks

Research Operations Lead

New York, NY

... and vendor contracts. You approach every workflow with a clarifying question: what truly needs ... Define our research ethics and data governance standards. Own the frameworks, consent workflows ...

Tekberry

Clinical Research Coordinator

Palo Alto, CA · On-site

$35 - $70/hr

Contract Schedule: Full-time, Monday - Friday | 8:00 AM - 5:00 PM Location: Stanford, CA 94305 ... Working knowledge of Good Clinical Practice (GCP) , informed consent, and research ethics.

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Clinical Research Coordinator

Clinical Research Coordinator

Winaxis

Boston, MA • On-site

$26.25 - $35/hr

Full-time

Posted 10 days ago

Job description

Job Summary: The Clinical Research Coordinator (CRC) is responsible for coordinating and managing clinical trials in accordance with study protocols, Good Clinical Practice (GCP) guidelines, institutional policies, and applicable regulatory requirements. The role involves participant recruitment, study documentation, data collection, and ensuring the smooth execution of research activities while safeguarding participant safety and data integrity. Key Responsibilities: Coordinate and oversee day-to-day activities related to assigned clinical studies. Review study protocols and ensure all trial activities are conducted in compliance with protocol requirements. Recruit, screen, and enroll eligible study participants according to inclusion and exclusion criteria. Obtain and document informed consent from study participants prior to study procedures. Schedule participant visits and coordinate study assessments, procedures, and follow-ups. Collect, document, and maintain accurate study data in Case Report Forms (CRFs) and Electronic Data Capture (EDC) systems. Maintain essential regulatory documents, investigator site files, and study records. Monitor participant safety by identifying, documenting, and reporting adverse events and serious adverse events in accordance with regulatory timelines. Coordinate with Principal Investigators, sponsors, Contract Research Organizations (CROs), laboratory personnel, and other study stakeholders. Prepare for and support sponsor monitoring visits, audits, and regulatory inspections. Ensure adherence to Good Clinical Practice (GCP), institutional policies, and applicable local and international regulations. Track study timelines, recruitment targets, and protocol milestones. Assist with study initiation, amendments, close-out activities, and archiving of study documents. Maintain confidentiality of participant information and research data at all times. Required Qualifications: Bachelor's degree in Life Sciences, Pharmacy, Nursing, Biotechnology, Medicine, or a related healthcare field. Prior experience in clinical research or clinical trial coordination is preferred. Certification in Good Clinical Practice (GCP) is an advantage. Required Skills: Strong understanding of clinical trial processes and research ethics. Knowledge of ICH-GCP guidelines and regulatory requirements. Excellent organizational and time-management skills. Strong verbal and written communication abilities. Attention to detail and accuracy in documentation. Proficiency in Microsoft Office applications and EDC systems. Ability to work independently and collaboratively within multidisciplinary teams. Effective problem-solving and interpersonal skills. Working Conditions: Work is typically performed in hospitals, research institutions, academic medical centers, or clinical research organizations. May require flexibility to accommodate participant schedules and sponsor visits.