Senior Clinical Research Coordinator
About the job
- A Bachelor of Science or Bachelor of Arts in Life Sciences or a related discipline and 4 years of experience as a Clinical Research Coordinator, or an Associate degree and 6 or more years of experience as a Clinical Research Coordinator, or a high school diploma and/or technical degree and 8 or more years of experience as a Clinical Research Coordinator.
- Experience performing clinical assessments, including obtaining vital signs, performing electrocardiograms, drawing blood, and processing and shipping laboratory specimens.
- Successful completion of Good Clinical Practice certification and Certified Clinical Research Coordinator certification is preferred.
- Maintain site compliance for all clinical-trial activities in accordance with established research protocols and standards and all applicable laws, regulations, policies, and procedural requirements.
- Maintain working knowledge of current Food and Drug Administration regulations, International Council for Harmonisation–Good Clinical Practice guidelines, organizational standard operating procedures, guidance documents, and assigned study protocols.
- Complete required organizational training, including International Council for Harmonisation–Good Clinical Practice certification and International Air Transport Association certification, in a timely manner.
- Lead, implement, and coordinate assigned clinical trials, including study start-up, vendor management, subject recruitment, source-document review and completion, protocol training, regulatory-document collection, participant visits, timely data collection and documentation, adverse-event and serious-adverse-event management and reporting, deviation reporting, monitoring visits, and follow-up.
- Create, collect, and submit regulatory documents to sponsors and Institutional Review Boards as required by the protocol, Good Clinical Practice and International Council for Harmonisation regulations, and Institutional Review Board requirements.
- Create patient-recruitment and study-execution strategies and ensure they are implemented to meet timelines and recruitment expectations.
- Ensure all team members follow good documentation practices when collecting, maintaining, and correcting study data and required records of clinical-trial activity, including source documentation, case report forms, queries, drug-dispensation records, and regulatory forms.
- Communicate with coworkers, leadership, study subjects, sponsors, contract research organizations, and vendors.
- Mentor and train staff in clinical-trial conduct, protocol requirements, communication, and trial-management skills.
- Collect and account for sponsor-provided supplies, including laboratory kits, ancillary supplies, and investigational products.
- Travel between company sites, meetings, or partner locations as required.
About the company
Profound Research is a clinical research organization that operates a nationwide network of trial sites, partnering with community physicians to bring pharmaceutical and biotech studies into everyday medical practices. It recruits and enrolls patients from a combined database of more than 1.25 million people, coordinates site operations and investigator oversight, and runs studies across more than 15 therapeutic areas on behalf of trial sponsors. Its network spans 22 sites across four geographies, with over 1,000 providers, 110-plus active investigators, and more than 130 clinical trials conducted to date. What sets Profound Research apart is its model of embedding research infrastructure within existing community practices, giving physicians and their patients access to experimental treatments without leaving their local care setting. The goal is to expand patient access to new treatments while helping sponsors conduct trials through a community-based site network.
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Simplify's Take
What believers are saying
- September 15, 2026 Series D raised $180 million at $1.8 billion valuation.
- June 13, 2026 and March 17, 2026 partnerships expanded Detroit and San Diego reach.
- Homepage claims 1.25 million patients, supporting faster recruitment than standalone sites.
What critics are saying
- Sequoia and Kleiner-backed competitors can outspend Profound after its September 2026 Series D.
- Growth depends on physician partnerships; one failed renewal disrupts enrollment and revenue quickly.
- No disclosed layoff issue exists, but 300+ staff and rapid hiring raise execution risk.
What makes Profound Research unique
- Embedded trial sites inside physician practices across 22 sites and 1,000 providers.
- Detroit and Southern California partnerships give direct access to prescreened patient pools.
- 130+ trials and 110+ investigators create operating leverage for sponsors and employers.
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Benefits
- Health Insurance
- Dental Insurance
- Vision Insurance
- Life Insurance
- Disability Insurance
- Health Savings Account/Flexible Spending Account
- Unlimited Paid Time Off
- Flexible Work Hours
- Remote Work Options
- Paid Vacation
- Paid Sick Leave
- Paid Holidays