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60 Icon Production Operations Manager Jobs Hiring Near You

Clinical Operations Specialist ICON is a global healthcare intelligence and clinical research ... Managing and maintaining comprehensive and accurate records of regulatory submissions, approvals ...

Manager, Laboratory

Farmingdale, NY · On-site

$91K - $114K/yr

As a Manager, Laboratory at ICON, you will oversee the day-to-day operations of the laboratory ... quality and productivity. * Managing laboratory budgets and resources, ensuring cost-effective ...

Clinical Operations Specialist ICON is a global healthcare intelligence and clinical research ... Managing and maintaining comprehensive and accurate records of regulatory submissions, approvals ...

Project Manager, IRT - United States (Remote) ICON is a global healthcare intelligence and clinical ... Collaborating with cross-functional teams, including clinical operations and technology specialists ...

Senior Product Manager

Austin, TX · On-site

$125K - $165K/yr

ICON is hiring a Senior Product Manager to plan, coordinate, and deliver BuildOS: our software ... Coordinate work across software, robotics, field operations, and business development. Speak up for ...

The Assistant Project Manager will play a key role in ensuring seamless coordination between design ... Coordinate with ICON's Design, Structural, MEP, and Print Operations teams to ensure design details ...

ICON is seeking a Logistics Analyst to manage end-to-end fleet operations and dispatching for raw ... Procure, lease, and lifecycle-manage fleet vehicles; coordinate with product programs on vehicle ...

ICON is seeking a Logistics Analyst to manage end-to-end fleet operations and dispatching for raw ... Procure, lease, and lifecycle-manage fleet vehicles; coordinate with product programs on vehicle ...

Production Team Lead

Farmingdale, NY · On-site

$19 - $26.25/hr

Performs additional responsibilities as requested by Management. * Reviews production reports daily to ensure KPI's are meet. Benefits of Working in ICON: Our success depends on the quality of our ...

You will serve as a key technical lead for external clinical supply operations, managing complex ... Employment with ICON is contingent upon having the legal right to work in the country where the ...

Clinical Operations Lead ICON is a global healthcare intelligence and clinical research ... As a Clinical Trial Manager at ICON, you will manage clinical trial operations activities ...

Demonstrated ability to provide operational management in the absence of senior management. * Willingness to travel as required (approximately 10%) #LI-MN1 #LI-REMOTE Employment with ICON is ...

Sr Project Manager, Laboratory ICON is a global healthcare intelligence and clinical research ... Senior Project Manager, Laboratory You will oversee clinical laboratory operations workstreams ...

Clinical Operations Manager - Regulatory - Montreal ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients ...

... Manager of Estimating. RESPONSIBILITIES: * Lead the preparation of detailed cost estimates ... Partner with ICON's Design Team, Build Operations, Print Operations, Material Supply Chain, and ...

... Manager of Estimating. RESPONSIBILITIES: * Lead the preparation of detailed cost estimates ... Partner with ICON's Design Team, Build Operations, Print Operations, Material Supply Chain, and ...

Clinical Operations Manager - Regulatory - Montreal ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients ...

Clinical Operations Lead ICON plc is a world-leading healthcare intelligence and clinical research ... As a Clinical Trial Manager at ICON, you will manage clinical trial operations activities ...

... the Manager of Estimating. Our ideal candidate is a highly analytical and detail-oriented ... Partner with ICON's Design Team, Build Operations, Print Operations, Material Supply Chain, and ...

Showing results 41-60

Clinical Operations Specialist

Raleigh, NC • On-site

Full-time

Medical, Dental, Vision, Life, Retirement

This job post has expired 1 day ago. Applications are no longer accepted.


Job description

Clinical Operations Specialist

ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.


As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.


As a Study Start Up Associate II at ICON, you will lead the initiation of clinical trials, ensuring compliance with regulatory requirements, and contribute to the advancement of innovative treatments and therapies.

What You Will Do:

You will contribute to site start-up and activation activities, taking responsibility for your deliverables and working collaboratively.
Key responsibilities include:

  • Leading the preparation and submission of regulatory documents, including clinical trial applications, ethics committee submissions, and regulatory agency communications.
  • Coordinating and liaising with internal and external stakeholders to obtain necessary approvals and authorizations for study initiation.
  • Managing and maintaining comprehensive and accurate records of regulatory submissions, approvals, and correspondence
  • Providing guidance and support to study teams on regulatory requirements and best practices for study start-up activities.
  • Participating in process improvement initiatives to streamline study start-up processes and enhance efficiency.

Your Profile:

You will bring relevant site start-up and activation experience, along with the following qualifications and skills.
Required qualifications and experience:

  • Bachelor's degree in life sciences or a related field.
  • Minimum of 2 years of experience in clinical research or regulatory affairs, with specific experience in study start-up activities.
  • Strong understanding of regulatory requirements and guidelines for clinical trials, including ICH-GCP and local regulatory requirements.
  • Excellent organizational and project management skills, with the ability to prioritize and manage multiple tasks simultaneously.
  • Excellent communication and interpersonal skills, with the ability to collaborate effectively with cross-functional teams.
  • Willingness to travel as required (approximately 5%)

Employment with ICON is contingent upon having the legal right to work in the country where the role is based.


Rewards & Benefits

ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.


Benefits may include:

  • Competitive base salary and performance related incentives
  • Health and wellbeing programmes including medical, dental, and vision coverage where applicable
  • Retirement and pension plans
  • Life assurance and disability coverage
  • Employee assistance programmes and wellbeing resources
  • Learning and development opportunities through structured training and career pathways

Benefits may vary depending on role and location.


Visit our careers site to read more about the benefits ICON offers.


Inclusion and Accessibility

ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.


If you require reasonable accommodations during the recruitment process, please let us know or submit a requesthere.

Are you a current ICON Employee? Please click here to apply