Senior Clinical Project Manager (Remote) at Jobgether

, , United States -

Full Time

Start Date

Immediate

Expiry Date

02 Feb, 26

Salary

173900.0

Posted On

04 Nov, 25

Experience

5 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Project Management, Regulatory Compliance, Clinical Research, Interpersonal Skills, Communication Skills, Study Design, Data Integrity, Publication Planning, Healthcare Collaboration, Clinical Operations, Attention to Detail, Scientific Expertise, Budget Management, Cross-Functional Communication, Stakeholder Management, Audit Support

Industry

Internet Marketplace Platforms

Description

This position is posted by Jobgether on behalf of a partner company. We are currently looking for a Senior Clinical Project Manager (Remote) in the United States. In this role, you will lead and coordinate global clinical projects to generate high-quality evidence supporting medical products and interventions. You will collaborate closely with internal teams and external stakeholders, including healthcare professionals and researchers, to design studies, ensure regulatory compliance, and deliver projects on time and within budget. This position requires a combination of scientific expertise, project management skills, and strong interpersonal abilities to oversee clinical evidence generation and facilitate cross-functional communication. You will contribute to publication planning, support clinical operations, and provide strategic insights that advance patient safety, data integrity, and organizational objectives. Accountabilities: Develop and manage global clinical evidence generation plans in collaboration with internal and external stakeholders. Oversee Investigator Initiated Study proposals, reviews, and execution. Support study design processes, including protocol development, in coordination with Clinical Operations and Data Sciences teams. Maintain relationships with Key Opinion Leaders and other clinical experts. Facilitate project communications, including status updates, resource needs, and key milestones. Support Clinical Research team interactions with regulatory authorities, notified bodies, and during audits. Contribute to publication planning, summaries, and dissemination of study results. Bachelor’s degree in health sciences; preference for biological sciences, engineering, or related medical/scientific fields. 6+ years of experience supporting clinical device research or equivalent medical device scientific projects. Knowledge of industry clinical research regulations and best practices (e.g., ISO 14155, ICH GCP). Strong project management and organizational skills with high attention to detail. Excellent interpersonal and communication skills to collaborate with cross-functional teams and external partners. Ability to work independently and manage multiple priorities effectively. Preferred Qualifications: Prior experience managing publication plans and contributing to scientific dissemination. Familiarity with clinical regulatory processes and documentation requirements. Competitive salary range: $105,500 - $173,900 USD, plus bonus eligibility. Comprehensive healthcare, dental, and vision benefits. Flexible remote work options with potential hybrid or onsite opportunities. Paid time off and support for work-life balance. Professional development and training opportunities. Travel opportunities (approximately 20% as required). Jobgether is a Talent Matching Platform that partners with companies worldwide to efficiently connect top talent with the right opportunities through AI-driven job matching. When you apply, your profile goes through our AI-powered screening process designed to identify top talent efficiently and fairly. 🔍 Our AI evaluates your CV and LinkedIn profile thoroughly, analyzing your skills, experience, and achievements. 📊 It compares your profile to the job’s core requirements and past success factors to determine your match score. 🎯 Based on this analysis, we automatically shortlist the three candidates with the highest match to the role. 🧠 When necessary, our human team may perform an additional manual review to ensure no strong profile is missed. The process is transparent, skills-based, and free of bias — focusing solely on your fit for the role. Once the shortlist is completed, we share it directly with the company that owns the job opening. The final decision and next steps (such as interviews or additional assessments) are then made by their internal hiring team. Thank you for your interest! #LI-CL1

Responsibilities

Lead and coordinate global clinical projects to generate high-quality evidence supporting medical products and interventions. Collaborate closely with internal teams and external stakeholders to design studies and ensure regulatory compliance.