Associate Director, Study Feasibility & Clinical Partnerships

About this role

About Care Access

Care Access is working to make the future of health better for all. With hundreds of research locations, mobile clinics, and clinicians across the globe, we bring world-class research and health services directly to communities that often face barriers to care. We 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 of tomorrow.

With programs like Future of Medicine , which makes advanced health screenings and research opportunities accessible to communities worldwide, and Difference Makers , which supports local leaders to expand their community health and wellbeing efforts, we put people at the heart of medical progress. Through partnerships, technology, and perseverance, we are reimagining how clinical research and health services reach the world. Together, we are building a future of health that is better and more accessible for all.

To learn more about Care Access, visit www.CareAccess.com .

How This Role Makes a Difference

Reporting to the Sr. Director of Study Feasibility & Clinical Partnerships, the Associate Director and Director of Study Feasibility & Clinical Partnerships provides strategic leadership for protocol and site feasibility across the Care Access Site Network and oversees the end-to-end lifecycle of clinical vendor partnerships that support Care Access objectives. This role is responsible for shaping and advancing feasibility strategy, ensuring robust site evaluation, and driving the identification, sourcing, qualification, onboarding, negotiation, and performance management of key vendors.

In close partnership with cross-functional teams, including Business Development, SSU, Finance, and Site Operation, this position guides data-driven feasibility assessments across the site network, leads cost-effective procurement strategies, strengthens contractual and operational frameworks, ensures regulatory and organizational compliance, and cultivates high-impact, high-performing vendor partnerships that enable successful study execution and organizational growth.

How You'll Make An Impact

Strategic Team Supervision and Development

• Provide leadership, supervision, and mentorship to Feasibility Managers and Vendor Acquisition Managers, fostering a collaborative, high-performing team environment.

• Promote professional development within the team, including training, coaching, and performance feedback.

• Establish and maintain strong, collaborative relationships with internal cross-functional teams and external vendors to ensure alignment, high performance, and seamless study execution.

• Contribute to continuous departmental improvement initiatives, including the development and optimization of tools, databases, processes, and best-practice SOPs to enhance operational efficiency and effectiveness

Clinical Trial Feasibility and Vendor Acquisition and Management Strategy

• Analyze and synthesize data from trial sponsors, CROs, and internal cross-functional teams to comprehensively understand study objectives, protocol requirements, and operational needs.

• Conduct comprehensive feasibility assessments of study protocols leveraging internal databases, trackers, and dashboards to assess feasibility across the Care Access Site Network, identify appropriate vendor scope, and ensure alignment of feasibility and vendor capabilities with study needs for optimal execution.

• Translate feasibility findings into actionable recommendations that guide strategic planning, vendor selection, and resource allocation to support efficient and effective study execution.

• Responsible for managing key vendor performance activities and contributing to the delivery of vendor performance management across development operations.

• Contribute to the maintenance and application of vendor performance management frameworks, including performance metrics, issue management practices, escalation pathways, and performance improvement approaches.

• Prepare and deliver performance analytics and reporting for vendors, translating performance data into actionable insights to support governance discussions and continuous improvement activities.

• Provide clear, decision-ready insights and recommendations to internal stakeholders and vendor partners based on analysis of performance data, issue trends, and operational inputs

• Proactively identify, escalate, and resolve feasibility- and vendor-related challenges that could impact clinical operations, timelines, or study deliverables.

Cross-Functional Collaboration and Strategic Input

• Partner with Business Development, SSU, Finance, Operations, Legal, and other stakeholders to align feasibility, vendor, and operational strategies with broader organizational objectives.

• Serve as a subject matter expert on feasibility and vendor considerations, providing insights and recommendations to support strategic decision-making.

Other Responsibilities

• Other duties as assigned based on evolving needs.

The Expertise Required

• Strong understanding of clinical protocols, general clinical research processes, start-up workflows, and Good Clinical Practice.

• Prior clinical research experience with the ability to discuss protocol clinical aspects with vendors and internal stakeholders.

• Excellent interpersonal, written, and verbal communication skills; ability to build relationships across dispersed teams.

• High level of professionalism, confidentiality, and sound judgment; able to make evidence-based decisions.

• Experience working with site networks, sponsors, and CROs; direct site-based experience strongly valued.

• Proven leadership, judgment, and decision-making skills in a fast-paced, matrixed environment.

• Ability to manage multiple priorities, competing deadlines, and cross-functional initiatives effectively.

• Demonstrated ability to negotiate and ‘sell’ Care Access’s value to vendors, sponsors, and in

Similar jobs

• Associate Director, Clinical Science — Natera · Remote
• Associate Director/Director of Preclinical Development — Kernalbio · Boston, MA
• Associate Director, Clinical Operations — Cogentbiosciences · Waltham, Massachusetts, United States
• Associate Director, Clinical Trial Management — Annexonbioscience · San Francisco Bay Area
• Executive Director, Clinical Development — Mineralystherapeutics · Remote
• Executive Director, Clinical Development — Centessapharmaceuticalsinc · Boston, MA
• Associate Director of Clinical Services — Centriaautism · Arizona, United States
• Associate Director of Clinical Services — Centriaautism · Tempe, Arizona, United States