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60 Imedica Clinical Program Manager Jobs Hiring Near You

EBR Systems, Inc.

Clinical Program Manager

The Clinical Program Manager serves as a key operational partner to the Head of Clinical Affairs, helping lead the Clinical Affairs function at EBR Systems. This role owns the end-to-end execution of ...

Intuitive

Clinical Program Manager

Sunnyvale, CA · On-site

The Senior Clinical Program Manager serves as the strategic and operational partner to Clinical Development & Operations leadership, providing integrated program management across the Clinical ...

Woodley House

Clinical Program Manager

Washington, DC · On-site

$90K/yr

The Clinical Program Manager is responsible for assuring quality services are provided to residents, coordination of day-to-day operations, completes authorization requests in conjunction with ...

IQVIA, Inc.

Clinical Program Manager

Durham, NC · On-site

$93K - $285K/yr

As Senior Project Leader/Clinical Program Manager you will liaise directly between IQVIA/sponsor functions and the customer, acting as that accountable point for delivery and quality whilst ...

IQVIA

Clinical Program Manager

Parsippany, NJ · On-site

$93K - $285K/yr

As Senior Project Leader/Clinical Program Manager you will liaise directly between IQVIA/sponsor functions and the customer, acting as that accountable point for delivery and quality whilst ...

Gilead

Clinical Program Manager

Foster City, CA · On-site +1

The Clinical Program Manager is responsible for the worldwide execution of all Phase I - IV clinical trials across all Gilead therapeutic areas. Clinical Operations plays a key role in ensuring all ...

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Infographic showing various Clinical Program Manager job openings at Imedica in the United States as of September 2026, with employment types broken down into 100% Full Time. Highlights an 96% Physical, and 4% Remote job distribution.

Clinical Program Manager

Manhattan, NY • On-site

Pivotal Solutions
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Re-posted yesterday

Job description

New York, United States | Posted on 09/02/2026

  • Industry Pharma/Biotech/Clinical Research
  • City New York
  • State/Province New York
  • Country United States
Job DescriptionPosition Overview

The Clinical Program Manager (CPM) is responsible for the strategic planning, oversight, and execution of clinical programs. The CPM ensures that all clinical trials within the program are conducted in compliance with the highest ethical standards and in accordance with applicable regulatory requirements.

Key ResponsibilitiesStrategic Planning and Oversight
  • Lead the development and execution of comprehensive clinical development plans.
  • Collaborate with cross-functional teams to ensure alignment of clinical objectives with company goals.
  • Monitor and assess the competitive landscape and adjust clinical strategies as necessary.
Clinical Trial Management
  • Oversee the design, planning, and implementation of clinical trials within the program.
  • Ensure that clinical trials are executed on time, within budget, and in compliance with Good Clinical Practice (GCP), regulatory requirements, and company SOPs.
  • Coordinate with clinical sites, CROs, and other vendors to ensure smooth trial execution.
Stakeholder Management
  • Serve as the primary clinical contact for internal teams, investigators, consultants, and regulatory agencies.
  • Foster strong relationships with key opinion leaders in the therapeutic area.
Data Management and Reporting
  • Oversee the collection, analysis, and interpretation of clinical data.
  • Ensure timely and accurate reporting of clinical trial results to regulatory agencies, as well as internal and external stakeholders.
Budget and Resource Management
  • Develop and manage the clinical program budget.
  • Ensure efficient allocation and utilization of resources across the clinical program.
  • Identify potential risks in clinical programs and develop mitigation strategies.
  • Ensure that all clinical activities adhere to safety and compliance standards.
  • Stay updated with the latest clinical research methodologies, regulatory requirements, and industry best practices.
  • Implement process improvements to enhance the efficiency and quality of clinical programs.
RequirementsQualifications
  • Bachelor’s degree in a related field; advanced degree (e.g., MD, PhD, PharmD) preferred.
  • Minimum of 7 years of experience in clinical research, with at least 3 years in a program management or leadership role.
  • Strong knowledge of GCP, ICH guidelines, and relevant regulatory requirements.
  • Proven track record of successfully managing complex clinical programs.
  • Excellent interpersonal, communication, and leadership skills.
  • Ability to work in a fast-paced environment and manage multiple priorities.
  • Proficiency in clinical trial management systems and related software.
Physical Requirements
  • Ability to travel as needed for site visits, investigator meetings, and conferences.
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