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Jobgether

Jobgether

via Lever.co

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Clinical Program Manager - REMOTE

Anywhere
Full-time
Posted 12/19/2025
Direct Apply
Key Skills:
Program management
Stakeholder engagement
Risk management
Data analysis

Compensation

Salary Range

$NaNK - NaNK a year

Responsibilities

Manage and oversee clinical trial activities from inception to completion, ensuring compliance and timely delivery.

Requirements

Bachelor's degree, 2-3 years clinical trial management experience, knowledge of FDA and EU regulations, excellent communication skills.

Full Description

This position is posted by Jobgether on behalf of a partner company. We are currently looking for a Clinical Program Manager. In this role, you will have the opportunity to manage and execute global clinical studies that make a difference in the medical field. Collaborating closely with the Clinical Affairs team, you'll ensure that all regulatory requirements are met while advancing innovative medical solutions. Your contributions will directly impact study performance and compliance, driving meaningful change for patients and healthcare providers. We're looking for an experienced professional who is ready to lead in a dynamic and fast-paced environment. \n Accountabilities Manage clinical trials from inception to Clinical Study Report completion. Ensure timely and budget-compliant completion of clinical trial activities in a dynamic environment. Create and implement study-specific clinical monitoring tools and documents. Lead the identification, evaluation, selection, and oversight of clinical trial sites. Author and implement operational plans for efficient study enrollment and monitoring activities. Review and approve vendor and site invoices, tracking study budget closely. Oversee the Trial Master File for inspection readiness. Drive cross-functional team support in the development of study documents. Lead the creation of project plans and reports. Review and approve site-specific documents and provide study updates. Conduct internal and external meetings, including Investigator Meetings. Provide oversight of ongoing study activities. Support study training for investigators and site staff. Participate in audits and regulatory inspections as needed. Perform additional duties as assigned. Requirements Bachelor's degree in a relevant field. 2-3 years of clinical trial management experience; IDE trial experience preferred. Minimum of 5 years of experience in the medical device industry. Knowledge of FDA and EU regulatory environments. Excellent written and verbal communication skills. Benefits Comprehensive benefits package including health, dental, vision insurance. Life, short-term, and long-term disability insurance. 401(k) plan. Paid time off and more. \n 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. #LI-CL1

This job posting was last updated on 12/21/2025

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