Conducts site monitoring across clinical studies, ensuring protocol and regulatory compliance while overseeing recruitment, data quality, site risks, trial documentation, and investigator collaboration.
Remote Mid-level Clinical Research Specialist Jobs
Search 27 active remote mid-level clinical research specialist jobs. No recruiters, no spam - just real jobs from real companies.
27 total jobs
7 new jobs this week
Country Regulatory Specialist, Clinical Research
Manage Brazilian regulatory and ethics submissions across clinical studies, serving as a key contact for authorities and committees while tracking approvals, maintaining documentation, and advising teams on local requirements.
Clinical Research Associate Manager - Neurology (Remote)
This role will be key to ensure strong monitoring in our clinical trials, managing a team of Clinical Research Associates to ensure excellent study performance and compliance.
Clinical Research Associate- Wound Care
Independently monitor wound care clinical trials, protect data integrity, and ensure protocol and regulatory compliance while coordinating with sites, sponsors, and clinical teams to support quality study delivery.
Clinical Research Associate- Wound Care
Oversee wound care clinical trials through site monitoring, data quality checks, regulatory compliance, safety reporting, and coordination with sponsors and research teams.
Sample Collector / Phlebotomist (Ad Hoc)
Collect hair, nail, blood and DNA samples at pre-booked appointments, using safe procedures and maintaining quality standards, client relationships and documentation that may support legal proceedings.
Site Manager (clinical research, local site coordinator role)
The Site Manager facilitates clinical studies by providing patient-related site support, ensuring compliance with protocols, and optimizing site staff performance.
Site Manager (clinical research, local site coordinator role)
The Site Manager facilitates clinical studies by providing patient-related site support and ensuring compliance with protocols and regulatory requirements.
Manage clinical trial activities across global projects, conducting site monitoring and supporting study startup while maintaining site relationships, patient safety, data quality, and compliance with study standards.
Conduct site monitoring across clinical studies, serving as the link between project teams, sponsors, and sites while protecting data integrity, protocol compliance, and study timelines.
Sr. Clinical Research Associate/Clinical trial Manager
As a Sr. Clinical Research Associate/Clinical Trial Manager, you will lead the operational management of clinical studies, ensuring compliance with protocols and regulations while collaborating with cross-functional teams.
Collects and evaluates clinical safety data, detects emerging risks, and supports pharmacovigilance documentation and risk management to protect patients and maintain regulatory compliance throughout drug development.
Clinical Scientist, Clinical Development
Supports clinical trial execution by contributing to protocol development, reviewing clinical data for safety and efficacy, preparing study documents, and collaborating across teams to maintain data quality.
Specjalista/ka laboratoryjny/a ds. Klienta (Mikrobiologia)
Manage client orders and data, advise on food and feed microbiological analyses, prepare and approve analytical reports, and support audits while following laboratory quality standards.
The Clinical Research Engineer will gain in-depth knowledge of FDA approved and investigational products, support training, and serve as a resource for clinical studies and protocols.
Clinical Research Associate II (Contract based)
Conducts clinical site monitoring and study oversight, managing site relationships, data quality, timelines, and regulatory support while protecting research participants’ rights, safety, and well-being.
Full-Time TVT/LAAO Clinical Data Abstractor (Hourly) Non-Exempt
Abstract and code patient information from medical records for TVT/LAAO registries, using EMR systems and maintaining accurate, consistent clinical data that meets registry requirements.
Manage assigned clinical trial monitoring and site activities, ensuring protocol, regulatory, and ICH GCP compliance while verifying source documents, documenting site findings, and escalating issues.
Administer and score autism and cognitive assessments across clinical locations, document evaluation findings, and collaborate with supervising psychologists to support diagnostic clarity.
Remote Healthcare Professional - Paid Focus Groups & Surveys
Participate in paid focus groups, clinical studies, and surveys, evaluating medical products and services and sharing detailed feedback to support healthcare research and product development.
Remote Healthcare Professional - Paid Focus Groups & Surveys
Participate in paid focus groups, clinical studies, and surveys, evaluating medical products and services and sharing detailed feedback during scheduled sessions.
Remote Healthcare Professional - Paid Focus Groups & Surveys
Participate in paid focus groups, clinical studies, and surveys, evaluating medical products and services and sharing detailed feedback to help inform healthcare decisions.
Remote Healthcare Professional - Paid Focus Groups & Surveys
Participate in paid focus groups, clinical studies, and surveys, evaluating medical products and services and sharing detailed feedback to support healthcare research and product development.
Remote Healthcare Professional - Paid Focus Groups & Surveys
Participate in paid focus groups, clinical studies, and surveys, evaluating medical products and services and sharing detailed feedback during scheduled sessions.
