Clinical Project Manager I/II

Symbio is a contract research organization supporting global studies across Dermatology, Inflammatory Diseases, Aesthetics, Rare Disease, Medical Devices, and Gastroenterology—from early development through regulatory approval.

Want to make an application Make sure your CV is up to date, then read the following job specs carefully before applying.

We are seeking a full-time Clinical Project Manager I or II to join our team in a fully remote role (with occasional travel). This individual will manage clinical trial projects from start-up through closeout, ensuring delivery against timelines, budget, scope, and regulatory requirements.

You will serve as the primary liaison between sponsors, internal teams, and vendors, and may participate in bid defense meetings. Strong global trial experience and comfort presenting to clients are essential.

Key Responsibilities:

• Lead planning and execution of clinical trial projects from proposal through closeout
• Act as primary sponsor liaison, ensuring alignment on scope, timelines, and deliverables
• Develop and maintain project management and study plans
• Coordinate cross-functional teams, vendors, and study stakeholders
• Support protocol development, study documentation, and regulatory deliverables
• Participate in feasibility, site selection, and bid defense activities
• Oversee training plans and study team readiness

Qualifications:

• Bachelor's degree in Business Administration, Science, or related field (or equivalent experience)
• 3+ years in pharmaceutical and/or clinical research industry
• 1+ years in clinical project management
• Demonstrated experience in managing low to moderate complexity trials
• Strong knowledge of GCP, ICH guidelines, and clinical trial regulations
• Excellent communication, time-management, and organization skills
• Ability to manage multiple priorities in a fast-paced environment
• Proficiency in Microsoft Office

Why Symbio? xhyhwjd

At Symbio, you'll join a collaborative and flexible environment where your work directly supports the successful delivery of global clinical research projects.

If you're passionate about advancing clinical trials and driving operational excellence, we'd love to hear from you.

Apply by sending your CV and cover letter to Jennifer Kidd at