Regional Lead Site Coordinator (South-West Region)

What You'll Do?

• Supervising tasks assigned to site-level staff.
• Serving as a resource for feasibility assessments for new and potential clinical studies.
• Conducting research-related visits according to study protocols.
• Cooking up research visit logistics, scheduling, and patient flow.
• Collaborating with ancillary departments involved in research activities.
• Assisting with general study conduct and data entry into EDC systems.
• Coordinating monitoring visits with CRO and sponsor representatives and resolving study-related issues.
• Providing backup Site/Study Coordinator support when needed.
• Maintaining compliance with GCP and regulatory requirements.
• Mentoring Milestone One and site staff.
• Developing protocol-specific tools and training materials.
• Supporting the development and maintenance of Milestone One's training program.
• Performing additional administrative responsibilities as assigned by the Milestone One Manager.

What We're Looking For:

• A university degree in Life Sciences, Pharmacy, Nursing, Laboratory Analytics, or a related field (Master's degree preferred).
• Current Good Clinical Practice (GCP) certification.
• International Air Transport Association (IATA) certification.
• Current Basic Cardiopulmonary Resuscitation (CPR) certification.
• Phlebotomy certification (unless included within an active RN or LPN license).
• Active Clinical Research Certification (ACRP, SOCRA, or another approved Clinical Research Organization).
• Demonstrated leadership skills with experience managing and training diverse teams.
• Strong communication and interpersonal skills.
• A thorough understanding of GCP and IRB/Regulatory requirements.
• Experience across multiple therapeutic areas.
• Ability to mentor colleagues and build strong relationships with clinical sites.
• Experience developing and maintaining site partnerships.