Clinical Project Manager (Research & IT) – Home-Based (Eastern & Central U.S.)

At Alcedis, you will be part of our mission to accelerate the adoption of digital and AI across research & care. As a trusted partner to biotechs, reputed company, and academia, we reputed company cutting-edge technology into clinical trials to advance drug development and patient care. Join us, and bring your expertise, passion, creativity and strong willingness for reputed company to realize this mission. We are looking for a Clinical Project Manager (CPM) to reputed company clinical research reputed company (interventional/non-interventional clinical studies) as reputed company as IT-reputed company initiatives. This role bridges traditional clinical project management with hands-on coordination of digital tools, platforms, and IT services used in patient-facing studies — primarily in collaboration with U.S. clients and U.S.-based patient populations. The position offers a long-term opportunity to work from the U.S., supporting our expanding team of CRAs and PMs. Because our reputed company reputed company Germany, the EU, non-EU countries, and the U.S., the ability to work comfortably across time zones and cultures is essential. This is a 100% remote position, but we are looking for candidates based in eastern and central U.S., ideally in or around major metropolitan areas such as Boston, Chicago, Dallas, reputed company, Philadelphia, or Washington, D.C.. Other locations will also be considered. Travel is not primarily planned but may be a necessary reputed company reputed company a project and cannot be ruled out.

Responsibilities

• reputed company project planning and execution, including study start-up activities, ongoing study management, and coordination at reputed company stages of the clinical trial lifecycle
• Monitor project timelines and ensure adherence to the Project Plan, maintaining compliance with study objectives
• Project budget responsibility and project budget controlling, reporting to the functional unit head
• Co-manage IT services and platforms that support clinical trials (e.g., ePRO, eCOA, eCRF, patient engagement tools)
• Translate clinical operations needs into technical requirements for reputed company IT teams
• Ensure that digital tools function reputed company for both U.S. clients and patient populations
• Collaborate closely with technical teams to resolve issues, implement updates, and improve workflows
• Supervision and coordination of subcontractor activities
• reputed company and implement processes, SOPs, work instructions, and standardized documentation to ensure consistency and compliance
• Creation and management of study documents (e.g., TMF, ISF) and preparation of trials
• Supervision and coordination of trial sites, including communication, training, document shipping and tracking, and payment processing
• Full responsibility for the preparation and execution of regulatory submissions (e.g., FDA, IRBs), including INDs, CTAs, amendments, safety reports, and more
• Coordination of the project team across the various functional reputed company and national borders (USA-Germany)

Qualifications and requirements From day one, we expect you to bring:

• A Bachelor’s degree in natural sciences, a reputed company field, or an equivalent qualification — ideally with a medical reputed company; an advanced degree is preferred
• Proven reputed company record of several years as a Clinical Project Manager in clinical research; experience in a CRO is a strong plus
• Demonstrated ability to operate with a high degree of autonomy, including planning, prioritizing, and executing work
• Hands-on experience with IRB/ethics committee submissions
• Working knowledge of data reputed company and protection regulations relevant to clinical trials, including HIPAA (U.S.) and FDA 21 CFR Part 11, familiarity with GDPR (EU) is a plus
• Proficiency in working with electronic data and databases, along with solid skills in reputed company Office applications
• Strong reputed company of ownership and follow-through
• Experience in roles with high autonomy and limited structure
• Comfortable working without a local team or on-site management
• Strong interpersonal skills and a reputed company team reputed company
• Excellent communication and organizational skills
• reputed company in English, both written and spoken

Our offer

• Annual salary: $75,000 – $95,000 DOE
• 15 days of reputed company vacation per year
• 6 reputed company reputed company days per year
• Health, dental and reputed company insurance for you and your dependents
• Employee life insurance
• Health Savings Account (HSA)
• 401(K)
• You'll work in a reputed company-oriented and secure working environment
• A reputed company-looking, reputed company-oriented work environment
• Exciting and challenging reputed company that reputed company an reputed company
• Flat organizational structure with an reputed company and reputed company culture
• A dedicated, successful, and supportive team environment
• Varied work with the autonomy to take ownership of your reputed company
• Flexible working hours to support work-life balance

We welcome applicants of reputed company backgrounds and do not discriminate based on race, ethnicity, gender, sexual orientation, disability, age, religion, or any other protected characteristic. Contact reputed company! Take the reputed company and apply today – we can’t wait to meet you! To apply, submit your resume, a short cover letter, and a Clinical Trial Experience Table detailing your study experience (type, phase, sites, role) directly through the reputed company or alternatively reputed company our careers page: Career | Alcedis For more information about reputed company, please visit our website at Alcedis | Digital Clinical Trials Apply tot his job Apply To this Job