Source Job

• Support and observe clinical site monitoring services inhouse.
• Provide monitoring and site management activities for full-service studies.
• Conduct remote data review, support data query and closure activities.

Alimentiv is a global contract research organization (CRO) providing clinical trials and research services. While the employee count is not provided, they appear to foster a collaborative environment.

• Ensure compliance with standard protocol and regulatory and ICH GCP obligations.
• Complete on-site and remote monitoring activities in compliance with the Clinical Monitoring Plan.
• Write and submit reports of investigational site findings and update applicable tracking systems.

Freenome is dedicated to changing the entire landscape of cancer. Freenome is an equal opportunity employer and values diversity.

• Performs on-site or remote monitoring visit activities.
• Identifies investigators and verifies qualifications.
• Trains investigational site staff as necessary.

Ergomed is a rapidly expanding full service mid-sized CRO specialising in Oncology and Rare Disease. Since its foundation in 1997 the company has grown organically and steadily by making strategic investments and landmark acquisitions, with operations in Europe, North America and Asia. Our company allows for employee visibility, creative contribution and realistic career development.

• Oversight of site level tasks associated with efficient site activation.
• Support the CRA team in preparing for site initiation visits (SIVs).
• Perform initial contract and budget negotiations with the sites, as well as amended where applicable

Fortrea helps to turn the impossible into I'm possible. They deliver exceptional service to their patients, fueled by a shared commitment to teamwork and excellence.

• Ensure the development and implementation of action plans.
• Lead regional/therapeutic area project resourcing.
• Develop, mentor, manage and coach GCM Managers.

Precision for Medicine is a global precision medicine clinical research services organization. They improve the clinical research and development process for new therapeutics by integrating clinical operations excellence, laboratory expertise, and advanced data sciences.

• Collect and interpret information from the Protocol, business development sold strategy & site feasibility team to prepare the site staff for site evaluation visits.
• Oversee the execution of Site Activation, site activation strategy, adhering to project timelines.
• Lead the process of study start-up to support site evaluation/selection visits on each new study and help get selected sites successfully activated and ready to consent.

Care Access is dedicated to making the future of health better for all by bringing world-class research and health services directly to communities. With hundreds of research locations, mobile clinics, and clinicians across the globe, they focus on ensuring every person has the opportunity to understand their health and access the care they need.

• Responsible for operational oversight of the site, site health and monitoring activities.
• Support sites in understanding study expectations, timelines, and required deliverables.
• Build and maintain strong, trusted relationships with investigators and site staff.

CSL Behring is a global biotherapeutics leader committed to saving lives. They focus on serving patients’ needs by using the latest technologies to discover, develop, and deliver innovative therapies. CSL's parent company, CSL, headquartered in Melbourne, Australia, employs 32,000 people and delivers its lifesaving therapies to people in more than 100 countries.

• Responsibility for day-to-day activities within a region or regions, including site selection, start-up, maintenance, and close-out activities.
• Serve as the key operational contact for Braveheart Bio studies aiding in site selection, study implementation, and ongoing coordination of study sites, either directly or via CROs.
• Proactively identify potential operational challenges and, in collaboration with senior team members, provide solutions to ensure study execution remains on track.

Braveheart Bio is a Bay Area–based biopharmaceutical company pioneering best-in-class therapies for cardiovascular disease. With a proven leadership team, a strong financial foundation, and a high-value late-stage asset, Braveheart Bio represents an outstanding opportunity for ambitious, mission-driven professionals to make a tangible impact in a rapidly evolving therapeutic area.

• Provide strategic and administrative leadership for clinical research business and operational activities.
• Ensure studies are conducted in accordance with regulatory requirements and sponsor expectations.
• Drive operational performance, program growth, and team development across the clinical research enterprise.

Florida Cancer Specialists & Research Institute (FCS) has built a national reputation for excellence since 1984. With over 250 physicians, 220 nurse practitioners and physician assistants and nearly 100 locations, they utilize innovative clinical research, cutting-edge technologies, and advanced treatments.

• Oversee and manage regional operational activities of global pivotal trials.
• Develop and oversee procedures for troubleshooting and problem solving.
• Maintain effective communication with vendors and internal departments.

Prilenia is a private biopharmaceutical company focused on developing transformative medicines for neurodegenerative diseases. With a highly committed and talented global team, they are developing pridopidine, an investigational neuroprotective therapy for ALS and Huntington’s disease.

• Assist in contacting investigator sites to provide study specific information.
• Ensure receipt, completeness and accuracy of clinical and administrative documents.
• Coordinate distribution and shipment of study-related materials.

Iovance Biotherapeutics aims to be the global leader in innovating, developing and delivering tumor infiltrating lymphocyte (TIL) therapy for people with cancer. They are pioneering a transformational approach to treating cancer by harnessing the ability of the human immune system to recognize and attack diverse cancer cells in each patient.

• Ensures complete study scoping, including testing requirements, facilities and other nuances.
• Provides technical details to study team for study designs and updates.
• Conducts investigations and assists with implementation of corrective actions, as needed.

ACM Global Laboratories impacts patients and their families by being purposefully patient-driven. Their dedication is reflected in the high-quality work provided by their teams every day around the globe.

• Lead clinical trial execution across the site network, overseeing study start-up, activation, and ongoing operational performance.
• Serve as the primary operational liaison for Sponsors and CROs, providing regular updates on study progress, risks, and mitigation strategies.
• Act as a central resource for site teams, resolving operational and protocol-related challenges and driving timely solutions.

Hawthorne Health is a leading community site network and home research visit solution provider, with 20+ sites and more than 2,000 research experienced healthcare professionals across the U.S. They leverage convenient, trusted, healthcare locations, identified patient data, and intelligent technology to accelerate patient access, improve retention, and reduce study costs.

• Interpret complex clinical study protocols.
• Develop and finalize global lab specification documents.
• Serve as a subject-matter expert for medical documentation.

ACM Global Laboratories contributes to patient well-being through high-quality work. They focus on being patient-driven and have teams globally.

• Prepare, compile, and submit regulatory documents to IRBs/ECs
• Support migration from Complion to Florence eRegulatory
• Maintain CVs, licenses, and GCP documentation

UniTriTeam is a global organization supporting clinical research sites and organizations through staff augmentation and technology solutions. They pride themselves on creating opportunities for their team members while delivering exceptional results for their clients.

• Analyze/annotate computed tomography angiography (CTA) images
• Support sites participating in clinical trials for the Cara System, including installation, case support, and data collection.
• Be accountable for day-to-day operations of the study(ies), ensuring adherence to study protocol, ICH/GCP, and other applicable regulations.

Cara Medical is a rapidly growing “Software as Medical Device” startup. They develop an innovative solution to noninvasively visualize the cardiac conduction system and personalizes and optimizes pacing and structural heart procedures.

• Independently prepare IRB documents, maintain regulatory files, and facilitate regulatory oversight of safety reporting.
• Prepare and review IND submissions, communicate with the FDA, and prepare for FDA audits.
• Lead study start-up/maintenance: prepare and submit all required regulatory documents for new/current study applications and successfully open/close studies from inception to accrual.

Emory University is a leading research university fostering excellence and attracting world-class talent to innovate today and prepare leaders for the future. They welcome candidates who can contribute to the excellence of their academic community.

• Identify, structure, and execute funded research collaborations and clinical partnerships.
• Translate scientific requirements into a site-friendly operational plan.
• Ensure GDPR/HIPAA-aligned processes, DPAs, data minimization, and participant withdrawal workflow.

Cephalgo is a Strasbourg-based technology company founded in 2020, developing AI solutions for safety, compliance, and trust in human-AI interactions. Backed by over €3 million in funding, they combine expertise in voice AI, data protection, and compliance to help enterprises build responsible AI systems.

• Contribute to the design and execution of research studies and evidence-generation activities.
• Work with product teams, research management professionals, and internal and external collaborators.
• Prepare project status updates and presentations for reporting to internal and external stakeholders.

Intuitive is a global leader in robotic-assisted surgery and minimally invasive care. Their technologies, like the da Vinci surgical system and Ion, have transformed how care is delivered for millions of patients worldwide. Intuitive's team of engineers, clinicians, and innovators are united by one purpose: to make surgery smarter, safer, and more human.

• Lead the planning/execution of clinical studies, aligning with regulatory/business objectives.
• Manage relationships with CROs, vendors, and external partners for timely/cost-effective study delivery.
• Project manage clinical trials, overseeing timelines, budgets, and deliverables.

Jobgether is a platform that helps connect job seekers with companies. They use AI-powered matching process to ensure applications are reviewed quickly, objectively, and fairly against the role's core requirements.