Source Job

• Monitor clinical studies of investigational and approved products.
• Manage and train site personnel on therapeutic area, protocol requirements, proper source documentation, and case report form completion.
• Review data queries and listings, and work with the study centers to resolve data discrepancies.

ProTrials is a women-owned, WBENC-certified Contract Research Organization (CRO) that has been a trusted partner in clinical research since 1996. They believe great work happens when team members feel valued, supported, and empowered, and they are committed to making a meaningful impact on global health.

• Performs on-site or remote monitoring visit activities.
• Identifies investigators and verifies qualifications and resources.
• Trains investigational site staff and supports regulatory submissions.

Ergomed is a rapidly expanding full-service mid-sized CRO specializing in Oncology and Rare Disease. The company has operations in Europe, North America, and Asia, fostering an international culture with employee well-being and career development opportunities.

• Develop, review, and update study-related training materials and documents.
• Serve as Subject Matter Expert for clinical sites and provide guidance on protocol interpretation and eligibility requirements.
• Partner with field Clinical Research Associates (CRAs) and CTAs to resolve issues identified during site visits.

ImmunityBio is a commercial-stage biotechnology company focused on developing cell and immunotherapy products designed to strengthen the immune system to eliminate cancerous or infected cells. They are publicly traded with headquarters in Southern California, working collaboratively to transform the lives of patients.

• 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.

• 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.

• Oversee clinical budgets and develop monitoring plans for effective study oversight.
• Train and mentor Clinical Research Associates (CRAs) to optimize their performance.
• Drive enrollment and lead study start-up activities, adhering to timelines.

Jobgether employs AI to match candidates to job openings, ensuring fair and objective reviews. They connect top candidates with hiring companies, who then manage the final decisions and interview process.

• Assist with daily site activities, acting as the primary point of contact for the site.
• Assist with training and mentoring research staff, upholding professional development goals.
• Promote strict adherence to ICH-GCP, FDA, and local regulations, maintaining audit readiness across all studies.

Care Access aims to improve the future of health for everyone. They operate globally with research locations, mobile clinics, and clinicians, bringing health services to communities, and are dedicated to ensuring every person can understand their health, access care, and contribute to medical progress.

• End-to-end management of the clinical trial agreement (CTA) process for global, multi-site clinical trials.
• Develop the study-specific CTA strategy with the Sponsor and internal stakeholders.
• Negotiate CTAs and the corresponding budget directly with clinical sites.

Jobgether uses an AI-powered matching process to ensure applications are reviewed quickly, objectively, and fairly. Their system identifies the top-fitting candidates, and this shortlist is then shared directly with the hiring company.

• Assess eligibility, interest, and availability of trial candidates via phone, email, and text.
• Communicate with site personnel to schedule visits and discuss program and participant statuses.
• Provide recruitment-related support and address questions or concerns from site personnel.

CrowdPharm, a Spectrum Science Company, focuses on delivering qualified trial candidates to clinical trial sites. While specific employee numbers aren't provided, Spectrum Science is a prominent player known for its collaborative and innovative culture.

• Directs the operational oversight and execution of clinical site start-up.
• Manages CRO relationship and oversight to ensure appropriate scope of work.
• Develops collaborative relationships with investigative sites.

Bristol Myers Squibb is focused on developing innovative drugs against targets of solid tumors. They are a dynamic biotechnology company headquartered in San Diego, CA, and aim to be the global leader in radiopharmaceuticals.

• Manage a portfolio of sponsor and client accounts, leading recurring calls, business reviews, and ad-hoc engagements.
• Drive responsiveness and service levels for sponsor requests, communicating with accuracy and awareness of business risks.
• Translate sponsor goals into cross-functional delivery plans.

Jobgether is a company that uses an AI-powered matching process to ensure your application is reviewed quickly, objectively, and fairly against the role's core requirements. They identify the top-fitting candidates, and this shortlist is then shared directly with the hiring company.

• Provide high level logistical support for clinical study operations, including study start up, study supplies, site qualification, site initiation, site management, study monitoring, and close out for clinical research studies and collaborations
• Develop study-related documents with minimal Clinical Trial Manager guidance including: protocol, informed consent forms, training materials, protocol amendments, monitoring plans, synopses, and ethics committee submissions, as required
• Manage small to medium size study contracting, budget, invoicing and payment process for all clinical trial vendors including investigative sites with minimal oversight

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 our work and each other.

• Manage a portfolio of accounts, leading recurring calls and business reviews.
• Translate sponsor goals into cross-functional delivery plans.
• Collaborate with Clinical Operations to improve sponsor experience.

Jobgether is a platform that uses AI-powered matching process to ensure applications are reviewed quickly, objectively, and fairly. They use an AI-powered matching process to ensure your application is reviewed quickly, objectively, and fairly against the role's core requirements.

• Directly manage a remote team of Care Partners, providing guidance and support.
• Design and improve operational processes to ensure high clinical quality.
• Monitor key performance indicators to measure success across different teams.

Medsien provides scalable remote care management for a quality patient experience. Hundreds of organizations trust Medsien's technology solutions to implement remote care management programs, personalize every interaction, and improve the lives of the people who need it most.

• Oversight for traveling clinical staff supporting decentralized operations at events and sites.
• Ensure high-quality protocol execution, participant safety, and adherence to GCP and FDA regulations.
• Manage, develop, and evaluate all clinical research staff (CRCs, nurses, mobile clinicians, and traveling staff).

Care Access aims to improve the future of health for everyone. With numerous research locations and clinicians globally, they deliver research and health services to communities facing barriers to care.

• Coordinate and assist with trial start-up activities.
• Facilitate resolution of laboratory queries.
• Track and report on study progress.

Freenome is dedicated to changing the landscape of cancer through early detection. They value diversity and do not discriminate based on various statuses protected by law.

• Manage retention work and deliver the highest quality customer experience.
• Build strong rapport with participants to help retain and engage them.
• Prepare participants for clinical studies through education using provided educational materials.

Care Access aims to improve the future of health for everyone. They have research locations and mobile clinics across the globe, they are dedicated to ensuring that every person has the opportunity to understand their health, access the care they need, and contribute to the medical breakthroughs.

• Ensure departmental compliance with all applicable global regulations and Sarah Cannon SOPs.
• Establish and lead the clinical operations strategy, setting departmental goals.
• Promote strong cross‑functional collaboration with internal stakeholders.

McKesson delivers products to healthcare providers. Every day, McKesson’s employees deliver products to healthcare providers that make a difference in the care and life of a patient, focused on creating an inclusive environment with strong values.