ICON plc

Senior Project Manager

ICON plc$100K — $130K *
Pharmaceuticals & Biotech
5 - 7 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's degree in a relevant scientific discipline or healthcare-related field
  • Extensive experience in project management within pharmaceutical or biotech industries, preferably in oncology and radiopharmaceuticals
  • Strong proficiency in project management tools and methodologies
  • Excellent analytical and problem-solving abilities
  • Demonstrated leadership skills, especially in mentoring teams
  • Exceptional communication skills for diverse audiences
  • Detail-oriented with strong organizational skills
  • Willingness to travel approximately 25% of the time

Responsibilities

  • Develop and execute clinical project plans for radiopharmaceutical and radioligand studies
  • Lead cross-functional teams for successful project implementation
  • Collaborate with stakeholders to identify project requirements and scope
  • Mentor and guide team members to foster excellence and improvement
  • Drive the development of project documentation and reports for stakeholders
  • Stay updated on industry trends and integrate best practices into project strategies
  • Contribute to organizational growth through effective project leadership

Benefits

  • Competitive base salary and performance-related incentives
  • Health and wellbeing programs, including medical, dental, and vision coverage
  • Retirement and pension plans
  • Life assurance and disability coverage
  • Employee assistance programs and wellbeing resources
  • Learning and development opportunities through structured training
Full Job Description
Senior Clinical Project Manager (Oncology Radiopharmaceuticals) - Remote, US

As a Senior Clinical Project Manager at ICON, you will be responsible for leading and manage projects, ensuring successful execution and delivery of project objectives, including those supporting radiopharmaceutical and radioligand-based clinical programs.

What You Will Do:

You will manage day-to-day project and program management activities, supporting your team to deliver quality outcomes.

Key responsibilities include:

  • Developing and executing clinical project plans, focusing on achieving project goals and objectives, including those for radiopharmaceutical and radioligand studies with specialized operational requirements.

  • Leading cross-functional teams to ensure the successful implementation of project activities.

  • Collaborating with stakeholders to identify project requirements and define project scope.

  • Mentoring and guiding team members, fostering a culture of excellence and continuous improvement.

  • Driving the development of project documentation and reports to present findings to stakeholders in a clear and actionable manner.

  • Staying abreast of industry trends and emerging technologies, including advancements in precision medicine, radiopharmaceuticals, and targeted oncology therapies, to integrate best practices into project management strategies.

  • Contributing to organizational growth through effective project leadership and strategic planning.

Your Profile:

You will have solid clinical project and program management experience, with the ability to manage competing priorities and develop your team.

Required qualifications and experience:

  • Bachelor's degree in a relevant scientific discipline or healthcare-related field

  • Extensive experience in project management, with a proven track record of leading successful projects in the pharmaceutical or biotech industry; experience in oncology, nuclear medicine, radiopharmaceuticals, or radioligand therapies is strongly preferred

  • Strong proficiency in project management tools and methodologies, with excellent attention to detail.

  • Excellent analytical and problem-solving skills, with the ability to develop effective project strategies.

  • Demonstrated leadership skills, with experience in managing and mentoring teams effectively.

  • Exceptional communication skills, with the ability to convey technical concepts to diverse audiences.

  • Detail-oriented, with strong organizational skills to manage multiple projects and deadlines in a dynamic environment.

  • Willingness to travel as required (approximately 25%)

#LI-MH1

#LI-REMOTE


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 to read more about the benefits ICON offers.

About ICON plc

ICON plc is a global provider of drug development and commercialisation services to the pharmaceutical, biotechnology and medical device industries. The company specialises in the strategic development, management and analysis of programs that support clinical development. ICON has approximately 15700 employees in 40 countries. The company was founded in Dublin, Ireland in 1990 and is headquartered in Leopardstown, Dublin. ICON has been publicly traded on the NASDAQ since 1998.
Learn more about ICON plc
Size
39,300 employees
Market Cap
$16.2 billion
Industry
Net Income
$332.3 million
Founded
2017
5 Year Trend
+26.9%
Revenue
$2.7 billion
NASDAQ

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