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.

• Monitor and own the progress of clinical studies at investigative sites.
• Ensure that clinical studies are conducted, recorded, and reported per protocol, SOPs, ICH-GCP, and all applicable regulations and standards.
• Coordinate all necessary activities required to set up and monitor a study (i.e., identify investigators; helping prepare regulatory submissions, conducting pre-study and initiation visits, etc.).

Precision for Medicine integrates clinical trial execution with deep scientific knowledge, laboratory expertise and advanced data sciences. They have a strong focus on Oncology and Rare Disease and passionate about cultivating their culture with high CRA retention rates.

• 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.

• 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.

• 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.

• 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.

• Independently oversees all aspects of study site management to ensure patient safety is protected.
• Independently conducts all forms of site visits, including pre-study/qualification, initiation, routine monitoring, and close-out visits.
• Develops and maintains good working relationship with investigators and study staff, serving as an ambassador to promote Precision's high quality and professional image.

Precision Medicine Group is expanding its capabilities across Latin America. They are an Equal Opportunity Employer, with employment decisions made without regard to race, color, age, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status or other characteristics protected by law.

• Assist Clinical Project Manager in the development and management of company-sponsored global clinical trials.
• Provide support in site recruitment, site initiation, site payments and site close-out.
• Help to provide guidance to clinical sites on a daily basis including protocol interpretation and protocol safety compliance.

ImmunityBio, Inc. is a commercial-stage biotechnology company that develops cell and immunotherapy products that are designed to help strengthen each patient’s natural immune system. The company is publicly traded with headquarters in Southern California, offering a collaborative environment with professional development opportunities.

• 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.

• Manages the financial, regulatory, patient management, and human resources functions associated with conducting clinical trials.
• Supervises a staff of 2 - 5 employees; trains new clinical trials staff; tracks enrollment, sponsor payments, and salary.
• Provides leadership in business development and assists residents in preparing research projects by facilitating IRB submissions and protocol writing.

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.

• Establishes and maintains a document management system for regulatory electronic files.
• Maintains FDA and GCP required regulatory documentation for individual sites, studies, sponsors and/or other networks.
• Modifies and/or develops informed consent forms and updates and manages protocol, investigator drug brochure and consent form modifications or amendments in compliance with IRB policy and HIPAA.

Sarah Cannon Research Institute (SCRI), a subsidiary of McKesson, is one of the largest community-based cancer programs advancing oncology treatments and improving outcomes for cancer patients globally. They look for mission-driven candidates who want to advance the fight against cancer and make a difference in patients' lives.

• Serve as leader of the local study team on assigned studies.
• Manage and maintain accurate country level plans including timelines and budgets.
• Implement startup and site activation plans at various levels.

Jobgether uses an AI-powered matching process to ensure applications are reviewed quickly, objectively, and fairly. They identify top-fitting candidates and shares this shortlist directly with the hiring company.

• 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.