Founded in 1992 and headquartered in Giessen, Germany, Alcedis brings more than 30 years of experience in clinical research. Today, we support clinical trials from Phase I through market approval as well as real-world evidence (RWE) studies, combining clinical data management and electronic data capture (EDC) with AI-driven data analytics and software platforms. Since 2023, Alcedis has been part of Huma Therapeutics. Join us, and bring your expertise, passion, creativity and drive to help us deliver on this mission.
We are looking for a Clinical Project Manager (CPM) to lead interventional and non-interventional clinical studies as well as related clinical technology initiatives.
This role combines classic traditional clinical project management with hands-on coordination of the digital tools, eClinical platforms (such as ePRO, eCOA, and eCRF), and IT services used in patient-facing studies. You will work primarily with U.S. clients and U.S. clinical trial sites.
The position offers a long-term opportunity to work from the U.S. and support our growing team of Clinical Research Associates (CRAs) and CPMs. Because our projects span Germany, the EU, non-EU countries, and the U.S., it’s essential that you’re comfortable working across time zones and cultures.
This is a 100% remote position open to candidates based in the Eastern or Central time zones (ET/CT). We prefer candidates located in or near major metropolitan areas such as Boston, Chicago, Dallas, New York City, Philadelphia, or Washington, D.C., but we welcome applications from anywhere within these time zones. The role is not travel-based, but occasional travel may be required depending on project needs.
Responsibilities
- Lead clinical trial planning and execution across the full study lifecycle, including study start-up, ongoing study management, preparation and management of study documentation (e.g., TMF, ISF), monitoring of project timelines, and ensuring adherence to the Project Plan and study objectives.
- Own project financial management, including responsibility for project budgets, budget control and reporting to the functional unit head.
- Lead regulatory submission activities, including the preparation and execution of submissions to the FDA, IRBs and other relevant authorities, such as INDs, CTAs, amendments and safety reports.
- Coordinate cross-functional and international project teams, working across functional units and national borders (U.S.–Germany), while supervising and coordinating subcontractor activities.
- Oversee clinical trial technology and digital platforms, including ePRO, eCOA, and eCRF; co-manage supporting IT services, ensure that solutions function effectively for U.S. clients and participants, and collaborate with technical teams to resolve issues, implement updates and continuously improve workflows.
- Develop and implement processes, SOPs, work instructions and standardized documentation to promote consistency, efficiency and regulatory compliance across clinical trial activities.
- Lead the coordination of clinical trial sites, including site communication, training, document shipment and tracking, and payment processing.
What you’ll bring:
- Education and clinical research experience
- Regulatory and compliance expertise
- Strong project ownership and autonomy
- Digital and data proficiency
- Collaboration and communication
- English proficiency
Our offer
- Base salary: $80,000 – $110,000 per year, DOE
- 15 days of paid vacation per year
- Paid holidays
- At least 6 paid sick days per year, or more where required by state or local law
- Health, dental and vision insurance for you and your dependents
- Employee life insurance
- Short term disability
- Long term disability
- Health Savings Account (HSA)
- 401(K) (no employer match)
- A forward-looking, growth-oriented work environment
- Exciting and challenging projects that make an impact
- Flat organizational structure with an open and collaborative culture
- A dedicated, successful, and supportive team environment
- Varied work with the autonomy to take ownership of your projects
- Flexible working hours to support work-life balance
Come join us! Take the next step and apply today – we can’t wait to meet you!
To apply, submit your resume directly through the link or alternatively via our careers page: Career | Alcedis. We look forward to getting to know you!
For more information about our company, please visit our website at Alcedis | Digital Clinical Trials.
Alcedis is an equal opportunity employer. We welcome applicants of all backgrounds and do not discriminate based on race, color, national origin, religion, sex (including pregnancy), sexual orientation, gender identity or expression, age, disability, genetic information, veteran status, or any other characteristic protected by federal, state, or local law.