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 clinical research project planning, execution, and delivery, ensuring regulatory compliance and quality.
Coordinate cross-functional teams and manage timelines, budgets, and study documentation.
Serve as the primary sponsor and client contact, providing regular project updates and resolving issues.
Alimentiv is a global CRO advancing therapies for gastrointestinal diseases, with deep expertise in IBD drug development. With about 700 employees across multiple countries, it is a private, profit-with-purpose company focused on scientific research and its people.
Provide administrative and regulatory support for the activation, maintenance, monitoring, and closeout of clinical research studies.
Assist Regulatory Coordinators with regulatory startup, continuing review, amendments, and study closeout activities.
Maintain study regulatory files and binders, ensuring documentation is complete, current, and audit-ready.
Fred Hutchinson Cancer Center is an independent, nonprofit organization providing adult cancer treatment and groundbreaking research focused on cancer and infectious diseases. Based in Seattle, Fred Hutch is the only National Cancer Institute-designated cancer center in Washington and operates eight clinical care sites with network affiliations in five states.
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.
Support Rater Training Program and serve as liaison across teams
Manage study reporting and ensure timely deliverable completion
Mentor junior team members and lead small studies
Cogstate advances brain health by providing digital cognitive assessments used in clinical trials and healthcare settings. With a global team of experts, the company supports over 2,000 clinical trials across 150+ countries in a collaborative, patient-first culture.
Lead data management activities from study start-up to database lock, ensuring quality and timelines.
Act as subject matter expert for DM in sponsor meetings and implement process improvements.
Mentor and train junior DM staff while managing project documentation, data validation, and system setup.
Fortrea is a global contract research organization providing clinical development and biometrics services to pharmaceutical and biotechnology companies. With a focus on teamwork and excellence, they foster a family-like culture where employees collaborate to advance life-saving therapies.
Provide medical oversight for clinical trials, safeguarding participant safety and ensuring protocol compliance.
Review adverse events and safety data, contributing to regulatory reporting and clinical documentation.
Collaborate with investigators and clinical teams to support study design, execution, and risk management.
This position is listed on behalf of a partner company that manages all applications and next steps. The role supports global clinical research in a remote working environment with cross-functional collaboration.
Manage and execute a portfolio of internal and external collaborative research studies for Intuitive Surgical's Digital products and services, with responsibility for project development, budgeting, and stakeholder management.
Oversee study documentation, compliance with regulatory requirements (GCP, ISO-14155, MEDDEV, MDR), and ensure audit readiness for all research projects.
Build and nurture relationships with external research partners, including surgeons, hospital leaders, and healthcare technology partners, to advance evidence-generation goals.
Intuitive is a global leader in robotic-assisted surgery and minimally invasive care, best known for the da Vinci surgical system. The company has been operating for nearly 30 years and fosters a culture of innovation and collaboration among engineers, clinicians, and innovators.
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.
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.
Train, mentor, and supervise junior Clinical Research Associates in their study-level responsibilities.
Conduct site selection, initiation, routine monitoring, and closeout visits for clinical trials.
Ensure regulatory compliance and data accuracy through CRF review and query resolution.
The partner company is a clinical research organization specializing in complex clinical studies. It fosters a people-focused culture with opportunities for professional growth and mentoring.
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.
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.
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.
Lead planning, execution, and oversight of clinical studies across Latin America.
Act as primary client contact and ensure compliance with ICH-GCP, SOPs, and regulatory requirements.
Mentor CRAs and partners while shaping country-level recruitment and monitoring strategies.
Precision Medicine Group provides clinical development, regulatory, and commercial solutions for life sciences companies. It fosters a collaborative, high-integrity culture with opportunities for growth and leadership in a global remote environment.
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.
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.
Coordinate planning, implementation, and delivery of device logistics projects for eCOA clinical trials.
Oversee budgets, deployment plans, and risk mitigation while collaborating with clinical teams and stakeholders.
Ensure inventory management, mobile device management, and global shipping are completed on schedule and within scope.
The hiring company is a life sciences organization specializing in device logistics and electronic clinical outcome assessments for clinical trials. They foster a collaborative, cross-functional remote culture aligned with US East Coast time zones.
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.
Lead Risk-Based Quality Management (RBQM) activities to ensure clinical trial quality and alignment with study objectives.
Oversee centralized monitoring, including developing Central Monitoring Plans, reviewing KRIs/QTLs, and maintaining dashboards.
Collaborate with global teams and sponsors to identify risks, recommend mitigations, and support inspection readiness.
A global clinical research organization focused on advancing medical innovation and improving patient outcomes through high-quality clinical trials. The company fosters a collaborative, multidisciplinary remote environment with international teams and a strong emphasis on regulatory compliance and data-driven decision-making.