Source Job

• Support the design, specifications, and development of eCRFs
• Develop Data Management Plan documents
• Manage effective communication of data issues and discrepancies to study sites via the query management process

Kyverna Therapeutics is a patient-centered, clinical-stage biopharmaceutical company developing cell therapies for patients suffering from autoimmune diseases. They are committed to transforming the future of treatment for autoimmune disease and redefining what’s possible.

• Provide leadership for the Data Management group and ensure quality data.
• Oversee DM vendors' deliverables and maintain strong collaboration.
• Create procedures for data collection, review, and cleaning processes.

Definium Therapeutics is a clinical-stage biopharmaceutical company focused on developing treatments for brain health disorders. They aim to be a global leader in delivering innovative treatments to improve patient outcomes and are expanding their global presence.

• Lead the end-to-end clinical data management strategy for Phase 3 and late-stage clinical trials.
• Provide hands-on oversight of CROs and external data management vendors, ensuring delivery against timelines, quality, and budget.
• Partner closely with Biostatistics to support interim analyses, database locks, and final clinical study reports.

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 high-profile and rapidly evolving therapeutic area.

• Leads data management activities for phase 1-4 studies.
• Manages and monitors progress with CROs and vendors.
• Reviews protocols for appropriate data capture and eCRF design.

Iovance Biotherapeutics is committed to cultivating and offering a diverse and inclusive work environment. As an equal-opportunity employer, their employees and applicants will be considered without regard to an individual’s race, color, religion, sex, pregnancy, national origin, age, physical and mental disability, marital status, sexual orientation, gender identity, gender expression, genetic information, military and veteran status, and any other characteristic protected by applicable law.

• Management and operational delivery of the clinical elements within a trial.
• Successful execution of assigned trials and ensuring completion of trial deliverables.
• Identify challenges to study timelines/deliverables and offer creative action plans.

Precision for Medicine is a precision medicine CRO with a uniquely integrated offering to enable the science of precision medicine. They achieve this by combining novel clinical trial designs, industry-leading operational and medical experts, advanced biomarker and data analytics solutions. They are dedicated to positively impacting the health and lives of patients around the world, particularly in rare diseases and oncology.

• Oversees all aspects of study site management to ensure patient safety is protected and quality of data is generated.
• Independently conducts all forms of site visits in accordance with the protocol, local laws, ICH-GCP and Precision SOPs.
• Communicates effectively and proactively with both site personnel and Precision Project and Clinical Trial Management.

Precision for Medicine is a precision medicine CRO that combines novel clinical trial designs, operational and medical experts, advanced biomarker and data analytics solutions, and a real passion for complex disease states. They strive to ensure employees feel appreciated through a multitude of benefits and value their ideas and contributions.

• Lead the planning, execution, and management of clinical trials.
• Ensure compliance with FDA, ICH-GCP, and other regulatory standards.
• Supervise and mentor Clinical Research Associates (CRAs) and study coordinators.

Jobgether leverages AI to match candidates with fitting roles, ensuring quick and fair application reviews. They connect top candidates directly with hiring companies, who then manage the final decision-making process.

• Manage and drive continuous process improvement initiatives.
• Oversee all daily, end to end, clinical trial/patient matching operations.
• Serve as a liaison between trial sites, sponsors, and drive project delivery.

Natera is a global leader in cell-free DNA (cfDNA) testing, dedicated to oncology, women’s health, and organ health. The Natera team consists of highly dedicated statisticians, geneticists, doctors, laboratory scientists, business professionals, software engineers and many other professionals from world-class institutions, who care deeply for their work and each other.

• Lead and oversee end-to-end clinical trial operations from study start-up through close-out.
• Develop and execute operational plans, timelines, and performance metrics to support successful delivery of assigned studies.
• Proactively identify operational risks and implement mitigation strategies to maintain timelines, quality, and compliance.

Centessa Pharmaceuticals plc is a new kind of pharmaceutical company with a deconstructed R&D environment that prioritizes data-driven decision-making led by subject matter experts. Their asset-centric model offers a unique R&D logic that has been applied by single-asset companies to improve productivity.