EPM Scientific
Base Pay Range
$120,000.00/yr - $150,000.00/yr
Direct message the job poster from EPM Scientific
Connecting Clinical Professionals with Exceptional Opportunities in the Biotech and Pharma Industries Base Salary: $150K USD + Bonus | Full-Time | Remote
Globally recognized, publicly traded full-service CRO that's redefining clinical research across continents. With a footprint in over 30 countries and a workforce of 10,000+, this organization partners with thousands of biopharma and medtech innovators to bring cutting‑edge therapies to market. From oncology to rare diseases, their pipeline is as diverse as their team. Leveraging AI‑powered platforms and real‑world data, they're not just conducting trials—they're shaping the future of medicine. If you're a Clinical Project Manager looking to lead global studies in a collaborative, tech‑forward environment, this is your chance to thrive.
Key Responsibilities
Lead and manage global Phase I-IV clinical trials across cardiovascular and oncology indications
Oversee cross‑functional teams including biometrics, regulatory affairs, medical writing, and pharmacovigilance to ensure seamless trial execution.
Develop and maintain project timelines, budgets, and risk mitigation strategies.
Serve as the primary point of contact for sponsors, vendors, and internal stakeholders.
Ensure compliance with ICH‑GCP, FDA, EMA, and local regulatory requirements.
Utilize AI‑enabled tools and platforms to optimize trial design and operational efficiency.
Contribute to business operations including budgeting, forecasting, and resource planning.
Mentor junior team members and foster a culture of excellence and innovation.
Qualifications
Minimum 10 years of experience in clinical research, with at least 6 years as a Clinical Project Manager.
Must have direct experience managing both cardiovascular and oncology studies.
Experience across multiple phases, preferably Phase II-III.
Global trial management experience is essential.
CRO experience strongly preferred.
Strong understanding of drug development processes and clinical trial regulations.
Valid and current GCP certification required.
Solid knowledge of local regulatory requirements in the U.S. and/or EU.
Proven experience in budgeting and business operations related to clinical project management.
Excellent communication, leadership, and problem‑solving skills.
If you or someone you know fits this experience and shows interest, we'd love to speak with you!
Seniority level
Mid‑Senior level
Employment type
Full‑time
Job function
Project Management
Industries
Medical and Diagnostic Laboratories
Referrals increase your chances of interviewing at EPM Scientific by 2x
#J-18808-Ljbffr
Direct message the job poster from EPM Scientific
Connecting Clinical Professionals with Exceptional Opportunities in the Biotech and Pharma Industries Base Salary: $150K USD + Bonus | Full-Time | Remote
Globally recognized, publicly traded full-service CRO that's redefining clinical research across continents. With a footprint in over 30 countries and a workforce of 10,000+, this organization partners with thousands of biopharma and medtech innovators to bring cutting‑edge therapies to market. From oncology to rare diseases, their pipeline is as diverse as their team. Leveraging AI‑powered platforms and real‑world data, they're not just conducting trials—they're shaping the future of medicine. If you're a Clinical Project Manager looking to lead global studies in a collaborative, tech‑forward environment, this is your chance to thrive.
Key Responsibilities
Lead and manage global Phase I-IV clinical trials across cardiovascular and oncology indications
Oversee cross‑functional teams including biometrics, regulatory affairs, medical writing, and pharmacovigilance to ensure seamless trial execution.
Develop and maintain project timelines, budgets, and risk mitigation strategies.
Serve as the primary point of contact for sponsors, vendors, and internal stakeholders.
Ensure compliance with ICH‑GCP, FDA, EMA, and local regulatory requirements.
Utilize AI‑enabled tools and platforms to optimize trial design and operational efficiency.
Contribute to business operations including budgeting, forecasting, and resource planning.
Mentor junior team members and foster a culture of excellence and innovation.
Qualifications
Minimum 10 years of experience in clinical research, with at least 6 years as a Clinical Project Manager.
Must have direct experience managing both cardiovascular and oncology studies.
Experience across multiple phases, preferably Phase II-III.
Global trial management experience is essential.
CRO experience strongly preferred.
Strong understanding of drug development processes and clinical trial regulations.
Valid and current GCP certification required.
Solid knowledge of local regulatory requirements in the U.S. and/or EU.
Proven experience in budgeting and business operations related to clinical project management.
Excellent communication, leadership, and problem‑solving skills.
If you or someone you know fits this experience and shows interest, we'd love to speak with you!
Seniority level
Mid‑Senior level
Employment type
Full‑time
Job function
Project Management
Industries
Medical and Diagnostic Laboratories
Referrals increase your chances of interviewing at EPM Scientific by 2x
#J-18808-Ljbffr