Remote Clinical Project Manager (US) – Digital Trials

your Jared; Buffalo (NY); Hybrid; USD 80,000 - 110,000; Full time

Benefits offered by this job

Health, dental and vision insurance

Health Savings Account (HSA)

401(K)

Flexible working hours

Paid vacation and sick days

Job summary

Alcedis is seeking a Clinical Project Manager to lead interventional and non‑interventional clinical studies and to coordinate IT services used in patient‑facing trials. The role primarily supports U.S.

clients and participants across time zones, with a long‑term, 100% remote arrangement in the Eastern or Central United States. The position requires 3–5+ years in clinical project management, with CRO experience, strong regulatory knowledge (FDA, IRB), and proficiency in digital platforms

Qualifications

• 3–5+ years of Clinical Project Manager experience in clinical research, with CRO exposure
• Experience leading interventional and non-interventional studies and coordinating IT components

Responsibilities

• Lead clinical trial planning and execution across the full study lifecycle
• Own project financial management including budgets and reporting
• Lead regulatory submissions to FDA, IRBs and other authorities
• Coordinate cross-functional, international project teams across US and Germany
• Oversee clinical trial technology and digital platforms (ePRO, eCOA, eCRF)
• Develop and implement standardized documentation and SOPs
• Coordinate site management, communication, training, document shipment and payments

Skills

Clinical project management

Regulatory submissions

Cross-functional collaboration

Digital platforms

English proficiency

Education

Bachelor’s degree in natural sciences or related field

Advanced degree preferred

Tools

Microsoft Office

Job description

Alcedis is seeking a Clinical Project Manager to lead interventional and non‑interventional clinical studies and to coordinate IT services used in patient‑facing trials. The role primarily supports U.S.

clients and participants across time zones, with a long‑term, 100% remote arrangement in the Eastern or Central United States. The position requires 3–5+ years in clinical project management, with CRO experience, strong regulatory knowledge (FDA, IRB), and proficiency in digital platforms