Project Manager I, IDEA

Posted 2 Days Ago
Be an Early Applicant
2 Locations
In-Office
Junior
Healthtech • Biotech • Pharmaceutical • Manufacturing
The Role
Manages endpoint adjudication processes for clinical trials, ensuring compliance with SOPs, ICH-GCP and study contracts. Delivers projects on time and on budget, develops and maintains adjudication documentation, leads internal processing teams, liaises with clients, performs UAT of adjudication systems, implements QC measures, and oversees reporting and finance-related activities.
Summary Generated by Built In
Project Manager I, IDEA

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.


We have an incredible opportunity for an Adjudication Project Manager to join ICON’s Independent DMC and Endpoint Adjudication (IDEA) team. The Adjudication Project Manager is primarily responsible for managing all endpoint adjudication processes for a clinical trial.

What you will be doing:

  • Manages project(s) in a timely manner in adherence with ICON's SOP's, ICH-GCP, and appropriate regulations
  • Delivers projects in accordance with the contract, timelines, and study budget
  • Identifies out of scope activities and initiates budget change orders and contract amendments
  • Performs project finance reporting activities
  • Attends and presents at Investigator Meetings, Client Kick-Off Meetings, and other client meetings
  • Performs user acceptance testing of electronic endpoint adjudication system
  • Ensures all necessary study specific training is provided to study team to improve performance and knowledge
  • Develops and maintains all trial documentation (i.e. Charter, Procedure Manual, Site Manual, Adjudication Forms, Communication Plan, System Requirement Specifications, Data Transfer Specifications, and Committee Training Manual) 
  • Serves as the primary study contact for client and internal and external study teams
  • Leads internal endpoint adjudication processing team
  • Develops and monitors endpoint adjudication processing workflows to maintain efficiency
  • Facilitates the development of project reports and distributes reports to the study team
  • Implements Quality Control measures for adjudication process and adjudication outcomes as necessary 

Your profile:

  • 2 years of project management experience in clinical research
  • Experience with timeline and budget management
  • Endpoint adjudication experience preferred
  • Strong written and verbal communication skills
  • Time management skills with the ability to prioritize efficiently
  • Detail-oriented
  • Bachelor’s degree

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 request here.

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

Skills Required

  • 2 years of project management experience in clinical research
  • Experience with timeline and budget management
  • Bachelor's degree
  • Strong written and verbal communication skills
  • Time management skills with the ability to prioritize efficiently
  • Detail-oriented
  • Endpoint adjudication experience

ICON plc Compensation & Benefits Highlights

The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about ICON plc and has not been reviewed or approved by ICON plc.

  • Healthcare Strength Benefits are described as comprehensive, with medical coverage and wellness initiatives highlighted. Larger sites are also associated with added wellness supports such as onsite fitness options and access to an employee assistance program.
  • Leave & Time Off Breadth Time-off and flexibility provisions are positioned as a meaningful part of the total package, including vacation/annual leave and flexible work scheduling. Flexibility is sometimes cited as helping offset long hours in certain roles.
  • Retirement Support Retirement and savings support is presented as a core component of the benefits package, including offerings such as pension arrangements in some locations and a U.S. 401(k) plan with company match. Financial planning resources are also emphasized as part of broader security benefits.

ICON plc Insights

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The Company
HQ: Dublin
34,685 Employees
Year Founded: 1990

What We Do

Since our foundation in Dublin, Ireland in 1990, our mission has been to help our clients to accelerate the development of drugs and devices that save lives and improve quality of life. We do this by delivering best in class information, solutions and performance, with an unyielding focus on quality at all times. We offer a full range of consulting, development and commercialisation services from a global network of offices in 53 countries. We focus our innovation on the factors that are critical to our clients – reducing time to market, reducing cost, and increasing quality – and our global team of experts has extensive experience in a broad range of therapeutic areas.

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