Clinical Research Associate​/Clinical Monitor​/Site Manager – Home-Based; Eastern U.S

Clinical Research Associate / Clinical Monitor / Site Manager – Home-Based (Eastern U.S.)

Join Alcedis, a HUMA company, for a Clinical Research Associate / Clinical Monitor / Site Manager – Home-Based position in the Eastern United States. This role focuses on site monitoring, protocol compliance, and overall study quality at investigational sites.

Base Pay: $75,000.00/yr - $95,000.00/yr

We are looking for candidates based in the Eastern U.S., ideally in or near major metropolitan areas such as Boston, New York City, Philadelphia, Pittsburgh, Columbus, Detroit, Atlanta, or Raleigh–Durham. Candidates located elsewhere in the Eastern U.S. will also be considered.

• Provide on‑site and remote support in the organization and conduct of studies and supervision of investigators.
• Prepare, conduct, and follow up on site initiation, monitoring, and close‑out visits (remote or on‑site).
• Assess study progress at assigned sites according to predefined guidelines and ensure complete, accurate documentation.
• Validate study data collected by investigators (source data verification).
• Prepare monitoring visit reports and related documentation.
• Evaluate study sites for compliance with applicable regulations, guidelines, and study protocols.
• Collaborate closely with data managers and project managers.
• Generate, track, and resolve queries.
• Train investigators and study coordinators in the use of EDC systems.
• Conduct feasibility assessments for new study sites and upcoming projects.
• Support and coordinate study sites, including assistance with documentation and escalation of site‑level issues.
• Prepare documents for submission to regulatory authorities and ethics committees.

• Bachelor’s degree in natural or life sciences or comparable qualification (e.g., Study Nurse certification).
• At least 3 years of hands‑on monitoring experience in GCP‑regulated interventional clinical trials.
• Working knowledge of data privacy and protection regulations relevant to clinical trials, including HIPAA (U.S.) and FDA 21 CFR Part 11; familiarity with GDPR (EU) is a plus.
• Ability to work independently, plan proactively, and execute tasks with foresight and attention to detail.
• Strong communication and organizational skills.
• Collaborative, team‑oriented mindset.
• Excellent written and spoken English.
• Willingness to travel and flexibility to support study needs.

• Annual salary: $75,000 – $95,000 DOE.
• 15 days of paid vacation per year.
• 6 paid sick days per year.
• Health, dental, and vision insurance for you and your dependents.
• Employee life insurance.
• Health Savings Account (HSA).
• 401(k) plan.
• Future‑oriented and secure working environment.
• Growth‑oriented work culture with autonomy and ownership of projects.
• Flexible working hours to support work‑life balance.

We welcome applicants of all backgrounds and do not discriminate based on race, ethnicity, gender, sexual orientation, disability, age, religion, or any other protected characteristic.

Submit your resume, a short cover letter, and a Clinical Trial Experience Table detailing your study experience (type, phase, sites, role) through the link provided in the job posting or via our careers page.

For more information about our company, please visit our website at Alcedis | Digital Clinical Trials.