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Clinical Research Site Director (Detroit, MI)*
Profound ResearchUnited Statesfull_timeVerifiedPosted 20 May 2025
About the role
Profound Research:Profound Research seeks to drive clinical innovation by partnering with community physicians to offer clinical research as a therapeutic option to their patients. Profound enables providers with the right people and tools to launch clinical research operations, often for the first time, to offer new care pathways to patients. Profound Research is looking to grow its energetic team inspired by changing how patients and providers engage in clinical research. Our Mission: Improving Lives by Providing Advanced Therapeutic Options Our Vision: Creating the Absolute Best Patient-Physician Experience in Clinical Research Our Values: Compassion: We value the patient-physician relationship above all else and are committed to a service-oriented approach to all interactions.
Urgency: We work hard and practice selflessness, acting swiftly and decisively to meet the needs of our patients, partners, and colleagues.
Solution Orientation: We are relentlessly positive, and we communicate directly to efficiently identify and implement effective solutions. Excellence: We insist on excellence, holding ourselves accountable and empowering each other to deliver best-in-class service while maintaining the highest ethical and scientific standards.
Profound Ethos o Physicians are the Vanguard o All Decisions Improve Patient Care o Never Compromise Quality
Role: Site DirectorCompany: Profound ResearchLocation: Detroit Metro, Michigan
Why this Role Exists The primary task of a site director (SD) is to manage all aspects of the clinical research program of thesite. The SD must be able to manage multiple trials and perform all tasks to execute, manage, andcoordinate research protocols, recruit subjects, data collection and operations of several concurrentclinical research studies. The SD will coordinate with the principal investigator(s) (PIs) and subinvestigator(s) to integrate their research tasks with the clinical schedule. Working under the directionof the PI, develop and maintain effective leadership and working relationships with all site personnel inaccordance with Profound’s policies and procedures. Responsible for guiding site with effectiveleadership skills, professional demeanor, and positive approach.
Responsibilities · Lead and execute clinical research studies and programs for the company.· Distill research protocols into research plans with timelines and delegation of duties toappropriate research staff.· Continually seek to improve site operations to enhance efficiencies to improve the overallprofitability of the site.· Conduct weekly site meetings to communicate information, provide continuing education,training and enhance teamwork.· Manage and establish external clinical/contract research organization (CRO) and clinical studysite relationships. Establish rapport and maintain contact and interact with monitors andsponsors to ensure customer satisfaction.· Manage and establish rapport with various persons involved in the study, including but notlimited to the patients, relatives/friends of the patients, doctors, pharmaceutical sponsors andall levels of the company.· Act as liaison between site and other departments within company (budgets/contracts, finance,regulatory).· Serve as main daily contact to PIs and Sub-Investigator(s).· Oversee the development, implementation, and updating of SOPs to ensure consistent, safe,and efficient management of clinical trials and continuous improvements in the fiscal integrity ofclinical research activities.· Lead the troubleshooting process to reach resolutions for any issues that arise during the courseof a study.· Maintain responsibility for the cost-effective requisition of needed equipment, supplies, andoutsourced services with acceptable
Urgency: We work hard and practice selflessness, acting swiftly and decisively to meet the needs of our patients, partners, and colleagues.
Solution Orientation: We are relentlessly positive, and we communicate directly to efficiently identify and implement effective solutions. Excellence: We insist on excellence, holding ourselves accountable and empowering each other to deliver best-in-class service while maintaining the highest ethical and scientific standards.
Profound Ethos o Physicians are the Vanguard o All Decisions Improve Patient Care o Never Compromise Quality
Role: Site DirectorCompany: Profound ResearchLocation: Detroit Metro, Michigan
Why this Role Exists The primary task of a site director (SD) is to manage all aspects of the clinical research program of thesite. The SD must be able to manage multiple trials and perform all tasks to execute, manage, andcoordinate research protocols, recruit subjects, data collection and operations of several concurrentclinical research studies. The SD will coordinate with the principal investigator(s) (PIs) and subinvestigator(s) to integrate their research tasks with the clinical schedule. Working under the directionof the PI, develop and maintain effective leadership and working relationships with all site personnel inaccordance with Profound’s policies and procedures. Responsible for guiding site with effectiveleadership skills, professional demeanor, and positive approach.
Responsibilities · Lead and execute clinical research studies and programs for the company.· Distill research protocols into research plans with timelines and delegation of duties toappropriate research staff.· Continually seek to improve site operations to enhance efficiencies to improve the overallprofitability of the site.· Conduct weekly site meetings to communicate information, provide continuing education,training and enhance teamwork.· Manage and establish external clinical/contract research organization (CRO) and clinical studysite relationships. Establish rapport and maintain contact and interact with monitors andsponsors to ensure customer satisfaction.· Manage and establish rapport with various persons involved in the study, including but notlimited to the patients, relatives/friends of the patients, doctors, pharmaceutical sponsors andall levels of the company.· Act as liaison between site and other departments within company (budgets/contracts, finance,regulatory).· Serve as main daily contact to PIs and Sub-Investigator(s).· Oversee the development, implementation, and updating of SOPs to ensure consistent, safe,and efficient management of clinical trials and continuous improvements in the fiscal integrity ofclinical research activities.· Lead the troubleshooting process to reach resolutions for any issues that arise during the courseof a study.· Maintain responsibility for the cost-effective requisition of needed equipment, supplies, andoutsourced services with acceptable
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