Perform site qualification, initiation, monitoring, and close-out visits ensuring regulatory and ICH-GCP compliance.
Verify informed consent, source documents, and CRF data accuracy, driving query resolution to closure.
Manage site-level activities, support recruitment, and maintain inspection-ready documentation.
Syneos Health is a leading fully-integrated life sciences services organization that partners with innovators across drug development and commercialization to accelerate progress. With over 25,000 colleagues globally, the company fosters an inclusive culture focused on career development, peer recognition, and a passion for delivering life-changing therapies.
Partner with cross-functional teams and study sites to support clinical operations across all trial phases.
Perform remote monitoring of clinical trials and serve as secondary contact for sites supporting CRAs.
Ensure proper reporting and follow-up of SAEs, address non-compliance issues, and assist with audit/inspection readiness.
Premier Research is a global clinical research, product development, and consulting company helping biotech, specialty pharma, and MedTech innovators turn breakthroughs into new treatments. The company fosters a collaborative culture focused on agility, continuous learning, and making an impact.
Manage and deliver clinical trial elements including site selection, start-up, enrollment, monitoring, data cleaning, and close-out.
Lead CRAs and oversee all clinical aspects of studies across multiple countries, ensuring timeline adherence and quality.
Identify risks, develop action plans, and maintain strong cross-functional communication to achieve client satisfaction.
Precision for Medicine is a precision medicine CRO that combines novel clinical trial designs, operational and medical experts, and advanced biomarker solutions for rare diseases and oncology. The company focuses on positively impacting patients' lives through targeted therapies and has a dynamic, high-energy culture.
Monitor and own study progress at sites, ensuring compliance with protocol, SOPs, ICH-GCP, and regulations.
Coordinate setup: investigators, regulatory submissions, pre-study and initiation visits.
Identify risks, propose mitigations, and become a protocol expert with a lower protocol load.
Precision for Medicine is a clinical research organization that combines novel clinical trial designs, advanced biomarker and data analytics, and specialized expertise in rare diseases and oncology. It is a smaller CRO with high CRA retention, a supportive culture, and a focus on giving employees influence and impact.
Conduct and report all types of onsite monitoring visits and be involved in study startup.
Perform CRF review, source document verification, and query resolution while managing site communication.
Support regulatory team in preparing documents and participate in feasibility research.
PSI is a leading Contract Research Organization with 30 years in the industry, offering a balance between stability and innovation to clients and employees. We focus on delivering quality and on-time services across a variety of therapeutic indications.
Coordinate clinical trial site activities and support successful site start-up and activation.
Serve as a primary point of contact for investigative sites, facilitating communication among clinical teams, sponsors, CROs, and regulatory stakeholders.
Ensure compliance with ICH/GCP guidelines, manage essential documentation, regulatory submissions, and site activation milestones.
This role is listed on behalf of a partner company in the clinical research sector, focused on coordinating site start-up and activation for clinical trials. The culture emphasizes operational excellence, collaboration, and patient safety, with a remote working environment.
Monitor clinical trial sites to ensure ethical, safe, and compliant conduct per protocol, GCP, and regulations.
Serve as primary liaison between Lycia and investigative sites for startup, maintenance, and close-out activities.
Manage regulatory documents, EDC data queries, and remote monitoring to maintain audit-ready TMF and CTMS records.
Lycia Therapeutics is a clinical-stage biotechnology company developing LYTAC-based therapeutics to degrade disease-driving proteins. It went public in 2026 and is headquartered in South San Francisco, California.
Independently conduct and document onsite and remote monitoring activities across Croatia, Serbia and Bosnia.
Serve as primary point of contact for investigative sites, ensuring compliance with protocols and regulations.
Mentor junior CRAs and collaborate with cross-functional teams to support study delivery.
Alimentiv is a global CRO focused on advancing therapies for patients with gastrointestinal diseases. With approximately 700 employees across multiple countries, it operates as a private, profit-with-purpose company, channeling commercial success back into research and people.
Conduct and report all types of onsite monitoring visits, including CRF review and source document verification.
Manage site communication and serve as the point of contact for in-house support services and vendors.
Support regulatory document preparation and participate in feasibility research for clinical studies.
We are a global CRO founded in 1995, working on the frontline of medical science to bring new medicines to patients. We bring together over 3000 dedicated professionals in a culture that cares for staff, clients, partners, and quality.
Monitor clinical studies at investigative sites to ensure compliance with protocols, SOPs, and ICH-GCP.
Coordinate study setup and initiation activities, including investigator identification and regulatory submissions.
Identify study risks and propose mitigation strategies while maintaining high quality and detail.
Precision for Medicine is a CRO integrating clinical trial execution with scientific expertise and data sciences, focusing on Oncology and Rare Disease. It offers a supportive, small-CRO culture with high CRA retention and emphasis on work-life balance.
Serve as primary TMF contact for assigned studies, ensuring files are complete and inspection-ready throughout the study lifecycle.
Develop and maintain study-specific TMF documents and provide training to internal and external stakeholders.
Perform periodic file inventories and reconcile expected document lists based on study milestones.
Alimentiv is a clinical services company specializing in Trial Master File (TMF) operations for clinical studies. They are a global organization with teams in multiple countries, fostering a collaborative and professional culture focused on quality and compliance.
Independently manage assigned clinical trial activities in compliance with GCP and regulations.
Oversee essential study documentation, TMF completeness, and study trackers.
Manage vendors, CTMS activities, and cross-functional coordination to ensure compliant study execution.
Cognito Therapeutics is a neurotechnology company developing a new therapeutic approach to cognitive and neurological health, including an investigational therapy for Alzheimer's disease. The company is an interdisciplinary team united by a shared purpose of protecting and progressing the human ability to think, learn and remember.
Lead data management activities for clinical trials, ensuring deliverables meet timelines and quality standards.
Create and review eCRF specifications, edit checks, and critical DM documents such as the Data Management Plan and Data Validation Plan.
Perform ongoing data review, reconciliation, database locks, and coordinate archiving of study databases.
ClinChoice is a global full-service CRO specializing in clinical development and functional solutions for pharmaceutical, biotechnology, medical device, and consumer health companies. With over 4,000 professionals in more than 20 countries, we maintain a quality-focused, collaborative one-team culture and below-average industry turnover.
Prepare, conduct, and report on all types of monitoring visits.
Ensure compliance with study protocols, ICH-GCP guidelines, and regulatory requirements.
Perform source data verification and manage site-level risks.
PSI is a leading Contract Research Organization with 30 years in the industry, offering a perfect balance of stability and innovation to clients and employees. We focus on delivering quality and on-time services across a variety of therapeutic indications.
Perform review and analysis of centralized data to identify signals and trends in predefined risk indicators.
Support initial review of Risk Assessment and Categorization Tool (RACT) and conduct periodic reviews of site-level Key Risk Indicators (KRIs).
Monitor site performance, evaluate quality and integrity of study practices, and maintain effective project communication on centralized monitoring findings.
Ergomed is a specialist clinical research organization focused on rare disease and oncology trials, partnering with small to midsize biotech companies to move therapies through early phase development. With a collaborative international team across North America, South America, Europe, Asia and Australia, we value teamwork, flexibility, and work-life balance, fostering a culture where employees take ownership and grow their careers.
Serve as the primary clinical point of contact with clients, overseeing the operational portion of clinical studies per scope of work.
Develop study-related clinical documents, train CRAs and vendors, and lead internal clinical team meetings to ensure trial compliance.
Drive site feasibility, recruitment and retention strategies, and manage eTMF, budgets, and vendor oversight to ensure quality and timelines.
Precision for Medicine is a CRO that integrates clinical trial execution with deep scientific knowledge, laboratory expertise, and advanced data sciences to improve the speed, cost, and success rate of bringing life-changing therapies to patients, with a strong focus on Oncology and Rare Disease. The company combines new technologies, operational scale, and a collaborative environment to support the life sciences industry.
Collaborate with project teams to support study startup and serve as primary point of contact for clinical sites.
Provide training on Beacon's devices and protocols, monitor progress, and maintain GCP/ICH compliance.
Address operational issues via Zendesk and Asana and deliver actionable site feedback for workflow improvements.
Beacon Biosignals is transforming precision medicine for the brain with at-home EEG and cardiopulmonary monitoring platforms for clinical development and diagnostics. They foster a remote-first culture with hubs in Boston, New York, and Paris, emphasizing curiosity, simplicity, and empathy.
Lead a centralized team of Data Coordinators to ensure accurate, timely, and complete clinical research data.
Manage workload, quality, and compliance for data activities across the Care Access site network.
Partner with clinical operations, sponsors, and CROs to resolve data issues and improve processes.
Care Access brings clinical research and health services directly to communities through hundreds of research locations and mobile clinics. They are dedicated to making health care more accessible and put people at the heart of medical progress.
Ensure compliance with study protocols, ICH-GCP guidelines, and regulatory requirements across assigned sites.
Conduct remote and on-site monitoring activities, including source document review and data verification.
Collaborate with site personnel and project teams to support oncology study delivery and inspection readiness.
Parexel is a leading global clinical research organization delivering insight-driven clinical and consulting solutions to the life sciences industry. With over 22,000 employees worldwide, they foster a collaborative, patient-focused culture dedicated to accelerating the delivery of new therapies.
Support the planning, coordination, and delivery of clinical research studies.
Collaborate with sponsors, cross-functional teams, vendors, and clinical sites to ensure studies meet timeline, budget, and quality targets.
Manage project milestones, site activation, patient recruitment, and risk mitigation in a remote working environment.
Jobgether is an AI-powered job matching platform connecting candidates with hiring companies. The hiring partner is a science-driven clinical research organization offering a collaborative remote environment.