Clinical Program Manager

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  • Company Jobgether
  • Employment Full-time
  • Location 🇺🇸 United States nationwide
  • Submitted Posted 1 week ago - Updated 14 hours ago

This position is posted by Jobgether on behalf of a partner company. We are currently looking for a Clinical Program Manager in United States.

This role offers a strategic opportunity for an experienced clinical professional to lead and manage global medical device studies. The successful candidate will oversee clinical trials from inception through study completion, ensuring compliance with regulatory standards and alignment with organizational goals. You will coordinate with cross-functional teams, manage study sites and vendors, and drive study performance while maintaining high-quality data and operational excellence. This position is ideal for a proactive, detail-oriented professional who thrives in a dynamic environment and is passionate about advancing innovative medical technologies to improve patient outcomes.


Accountabilities:
  • Manage all phases of clinical trials, from study design to Clinical Study Report (CSR) completion.
  • Oversee site selection, qualification, activation, training, and monitoring to ensure study compliance and performance.
  • Collaborate with vendors and internal teams, including finance and clinical operations, to manage budgets, invoices, and timelines.
  • Develop and implement operational plans, monitoring tools, and study documents such as protocols, consent forms, and project plans.
  • Lead internal and external meetings, investigator meetings, conferences, and study management sessions.
  • Conduct ongoing data reviews, cleaning, and quality oversight to ensure integrity of study results.
  • Support training initiatives for investigators, site staff, and internal teams.
  • Participate in audits, regulatory inspections, and continuous process improvement initiatives.
Requirements:
  • Bachelor’s degree in a relevant field; advanced degrees preferred.
  • Minimum of 2–3 years of clinical trial management experience; IDE trial experience preferred.
  • At least 5 years of experience in the medical device industry.
  • Strong knowledge of FDA and EU regulatory environments and ICH/GCP requirements.
  • Proven ability to manage complex, global studies and cross-functional teams.
  • Excellent written and verbal communication skills, with strong organizational and problem-solving abilities.
  • Ability to travel up to 25% of the time, including day trips and overnight stays.
  • Demonstrated attention to detail, initiative, and ability to work in a fast-paced, dynamic environment.
Benefits:
  • Comprehensive health, dental, and vision insurance.
  • Life, short-term, and long-term disability insurance.
  • 401(k) retirement plan.
  • Paid time off and holidays.
  • Flexible remote work with occasional travel as required.
  • Opportunities for professional growth and skill development.


Why Apply Through Jobgether?

We use an AI-powered matching process to ensure your application is reviewed quickly, objectively, and fairly against the role's core requirements. Our system identifies the top-fitting candidates, and this shortlist is then shared directly with the hiring company. The final decision and next steps (interviews, assessments) are managed by their internal team.

We appreciate your interest and wish you the best!


Data Privacy Notice: By submitting your application, you acknowledge that Jobgether will process your personal data to evaluate your candidacy and share relevant information with the hiring employer. This processing is based on legitimate interest and pre-contractual measures under applicable data protection laws (including GDPR). You may exercise your rights (access, rectification, erasure, objection) at any time.

 


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