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.
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.
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.
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.
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.
Perform on-site or remote Pre-Study, Initiation, Interim, and Close-Out monitoring visits to ensure sites are adequate for study conduct.
Verify investigator qualifications, resources, facilities, equipment, and staff for clinical study conduct.
Train site staff, support regulatory/EC submissions, and mentor junior staff during co-monitoring visits.
Ergomed Group is a global clinical research organization helping biopharmaceutical companies develop and deliver therapies in oncology, rare disease and other complex areas. Its diverse teams across countries and time zones collaborate with kindness, curiosity and a shared sense of purpose.
Manage all clinical operational aspects of global trials including start-up, conduct, and close-out.
Oversee CRO and site adherence to GCP and SOPs, proactively identifying and resolving study risks.
Lead study team meetings, build investigator relationships, and support protocol development.
Vera Therapeutics is a commercial-stage biotech focused on transforming autoimmune disease treatment, starting with the kidney. Founded in 2016 in Brisbane, CA, the company values empathy, ownership, clarity, and urgency in a collaborative, fast-paced team.
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.
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.
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.
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.
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.
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.
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.
Lead, coach, and develop Site Directors and Site Managers with clear goals, KPIs, and expectations.
Monitor site operations and performance metrics to improve quality, enrollment, and protocol compliance.
Partner with site leadership on budgeting, forecasting, FTE planning, and margin management.
M3 Wake Research is a network of clinical research sites for pharma, biotech, and device companies. It has nearly 30 U.S. sites and 7,000+ completed trials, making it one of the largest independent multi-site clinical research companies.
Independently manage site monitoring activities for wound care clinical trials, ensuring data integrity and GCP compliance.
Collaborate with sponsors, investigators, and cross-functional teams to resolve issues and support effective trial delivery.
Contribute to study planning, regulatory documentation, audit readiness, and patient recruitment oversight.
The company is a clinical research organization focused on wound care trials. It offers a collaborative, international, and innovation-driven culture with opportunities for professional development and flexible remote work.
Lead GCP quality for clinical studies as the primary Quality point of contact from start-up through close-out.
Build the GCP quality framework, authoring SOPs, quality plans, and risk management aligned with ICH E6(R3).
Qualify and audit CROs, clinical sites, and vendors, and partner on inspection readiness.
Osanni Bio is a development-stage therapeutics platform headquartered in San Francisco, California, advancing programs in ophthalmology, cardiology, and beyond. They are a creative, agile team of innovators guided by core values of integrity, impact, agility, and collaboration.
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.
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.
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.