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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:
clinical trial management
regulatory compliance
project management
study documentation
vendor oversight

Compensation

Salary Range

$0K - 0K a year

Responsibilities

Manage and oversee global clinical studies ensuring compliance, quality, and timely completion.

Requirements

Bachelor's degree, 2-3 years of clinical trial management experience, 5+ years in the medical device industry, knowledge of FDA/EU regulations, strong 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 develop, manage, and execute global clinical studies, playing a crucial part in ensuring compliance with regulatory requirements. Your expertise will help enhance study performance and streamline operations. This position allows for significant input into trial design and management, making a meaningful impact on the advancement of medical technology and patient care. \n Accountabilities Manage clinical trials from inception to completion of Clinical Study Report (CSR) Ensure timely and budget-compliant trial activities in accordance with quality standards Create and implement study-specific monitoring tools and documentation Lead the selection and oversight of clinical trial sites Author and implement operational plans for study enrollment and monitoring Review vendor and site invoices, tracking study budget in collaboration with finance Oversee Trial Master File for inspection readiness Support cross-functional teams in developing study documents Create project plans, logs, templates, and newsletters Review and approve site specific documents such as consent forms and budgets Provide study updates and reports detailing risks and issues Lead internal and external meetings, including Investigator Meetings Conduct ongoing study data reviews and data cleaning activities Oversee site initiation, data quality, and close out activities Develop training for investigators and site staff Participate in internal process audits and regulatory inspections Other duties as assigned Requirements Bachelor's degree in a relevant area of study 2-3 years of clinical trial management experience; IDE trial experience preferred Minimum of 5 years' experience in the medical device industry required Knowledge of FDA and EU regulatory environments Excellent written and verbal communication skills Benefits Comprehensive benefits package including health, dental, and vision insurance Life, short-term, and long-term disability insurance 401(k) plan Paid time off Equal opportunity employer, valuing diversity and inclusion \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 12/19/2025

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