JUMP TO CONTENT
Shortlist
search jobs Search
About the role ICON and you Application Process Day in the life Who we are

Senior Project Manager - Oncology/Biotech (Home-based)

059130_2

About the role

This vacancy has now expired. Please click here to view live vacancies.
Are you ready to be a part of a successful study delivery team? ICON’s award-winning study execution capabilities have led to the approval of 18 of the world’s top 20 best-selling drugs. Make your experience count for the benefit of patients worldwide.

Location: Any US location (Home or Office Based)

At ICON, it’s our people that sets us apart.

As a Senior Project Manager within our Oncology/Biotech team, you will expect to add towards a culture of project group excellence with a focus on process improvement, adding value and exceeding client needs.
You will be the point of contact for designated projects, responsible to deliver successful client relationships, lead cross-functional teams, define project scope, build resource requirements, risk migration strategies, associate action plan and issue resolution. You will lead global trials within a therapeutically aligned team across a variety of complex indications. As a Project Manager, you are involved at the forefront of innovation and drive delivery using your project leadership expertise.

Our projects range from phase II safety and efficacy trials to large scale outcomes mega-trials. You have the support of extraordinary, tenured and experienced leadership whose goal is to help you apply and expand your project management, drug development and therapeutic expertise.

The Role:

  • Run a cross functional project team ensuring all necessary delivery of project training and developing a succession plan for the core team members
  • Manage project study budgets and invoicing procedures according to study contract
  • Report progress of projects to ICON clients and monitor and implement QC activities as necessary
  • Collaborate with business development to ensure we have a dedicated commercial aptitude and work together with internal colleagues and external partners to identify new avenues for growth

Role Requirements:

  • Bachelor’s Degree in science, business, medicine or equivalent degree
  • Project Management or equivalent (PMI certification) is desirable
  • At least 2 years PM experience within clinical research and study operations
  • Experience in working on a wide range of Oncology/Biotech indications 
  • Comprehensive knowledge of ICH-GCP
  • Strength in communication, planning, decision-making, negotiation, conflict management and time management skills
  • Willingness to travel up to 25% as needed

Benefits of Working in ICON:

ICON provides Project Managers with the creative resources to be successful in delivering results, inspiring others and becoming a trusted partner. We offer a competitive benefits package that includes a comprehensive health plan, retirement plan, highly competitive pay, corporate bonus plan, 5 weeks PTO, and many other incentives, as well as the opportunity to grow your career within our Project Management team.

You will be joining us at the very right time – we're listed on the Forbes Best Employers of 2018, for the second year in a row!

What’s Next?
Take the next step by applying and one of our dedicated recruiters will follow up to share more details about this opportunity.

ICON is an equal opportunity employer - Minorities/Females/Disabled/Veterans and committed to providing a workplace free of any discrimination or harassment.

List #1

Day in the life

Liquid drug vials in palm of hand
Understanding INDs and NDAs in Clinical Research

Teaser label

Industry

Content type

Blogs

Publish date

04/22/2025

Summary

What is an IND or NDA? A Guide for Aspiring Clinical Research Professionals If you’re considering a career in clinical research or the broader pharmaceutical and biotech industry, you’ve likely c

Teaser label

Discover the difference between IND & NDA applications, and the steps from drug development to regulatory approval.

Read more
Informed consent form
What is an Informed Consent Form (ICF)?

Teaser label

Industry

Content type

Blogs

Publish date

04/22/2025

Summary

When it comes to clinical trials, one of the most important documents you’ll hear about is the Informed Consent Form (ICF). Whether you're starting out in clinical research or exploring job opportunit

Teaser label

Learn what an Informed Consent Form (ICF) is, why it’s essential in clinical research, and how it protects participants.

Read more
Medic in full gown with a clipboard
Clinical Research Associate (CRA) vs Clinical Research Coordinator (CRC)

Teaser label

Industry

Content type

Blogs

Publish date

04/17/2025

Summary

CRA vs CRC Embarking on a career in clinical research is an exciting journey for STEM graduates, offering opportunities to contribute directly to the development of new therapies and to safeguard

Teaser label

Discover the key differences between Clinical Research Associates (CRA) and Clinical Research Coordinators (CRC).

Read more
View all

Similar jobs at ICON

Validation Engineer

Salary

Location

Mexico

Department

Clinical Operations Roles

Location

Mexico

Remote Working

Remote

Business Area

ICON Strategic Solutions

Job Categories

Clinical Trial Support

Job Type

Permanent

Description

We are currently seeking a Validation Engineer to join our diverse and dynamic team. In this role at ICON, you will be responsible for executing validation activities for equipment, systems, and proce

Reference

2025-118361

Expiry date

01/01/0001

Rita Villavicencio

Author

Rita Villavicencio
Rita Villavicencio

Author

Rita Villavicencio
Read more Shortlist Save this role
Read more Shortlist Save this role
Front-End Developer

Salary

Location

Brazil, Sao Paulo

Location

Sao Paulo

Mexico City

Remote Working

Hybrid: Office/Remote

Business Area

ICON Full Service & Corporate Support

Job Categories

Patient Recruitment

Job Type

Permanent

Description

At ICON, it’s our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to fulfil our mission to advance and improve patients’ lives. Our ‘Own I

Reference

JR128404

Expiry date

01/01/0001

Olivia Molina

Author

Olivia Molina
Olivia Molina

Author

Olivia Molina
Read more Shortlist Save this role
Read more Shortlist Save this role
Biosample Operations Specialist

Salary

Location

United States

Department

Clinical Operations Roles

Location

United States

Remote Working

Remote

Business Area

ICON Strategic Solutions

Job Categories

Clinical Trial Support

Job Type

Permanent

Description

The Biosample Operations Specialist is responsible for overseeing the biomarker laboratory samples for the client's clinical trials across the chain of custody from research site to the analysis labor

Reference

2025-118494

Expiry date

01/01/0001

Kala Murphy

Author

Kala Murphy
Kala Murphy

Author

Kala Murphy
Read more Shortlist Save this role
Read more Shortlist Save this role
Medical Research Associate

Salary

Location

US, Lenexa KCI (PRA)

Department

Full Service - Early Clinical and Bioanalytical Solutions

Location

Lenexa

Remote Working

Office Based

Business Area

ICON Full Service & Corporate Support

Job Categories

Clinic

Job Type

Permanent

Description

We are currently seeking a Medical Research Associate to join our diverse and dynamic team. As a Medical Research Associate at ICON, you will be responsible for meeting/greeting clinical research volu

Reference

JR128255

Expiry date

01/01/0001

Kahla Cureton

Author

Kahla Cureton
Kahla Cureton

Author

Kahla Cureton
Read more Shortlist Save this role
Read more Shortlist Save this role
Clinical Research Nurse I

Salary

Location

US, Lenexa KCI (PRA)

Department

Full Service - Early Clinical and Bioanalytical Solutions

Location

Lenexa

Remote Working

Office Based

Business Area

ICON Full Service & Corporate Support

Job Categories

Nurse

Job Type

Temporary Employee

Description

We are currently seeking a Clinical Research Nurse I to join our diverse and dynamic team. As a Clinical Research Nurse I at ICON, you will play a pivotal role in supporting the execution of clinical

Reference

JR125862

Expiry date

01/01/0001

Muna Nelke

Author

Muna Nelke
Muna Nelke

Author

Muna Nelke
Read more Shortlist Save this role
Read more Shortlist Save this role
Clinical Trial Manager - Medical Affairs

Salary

Location

Brazil

Department

Clinical Trial Management

Location

Brazil

Remote Working

Remote

Business Area

ICON Strategic Solutions

Job Categories

Clinical Trial Management

Job Type

Permanent

Description

This role is key to the success and consistency of delivery of the clinical phase of the project. Primary point of contact for clinical deliverables for both internal and external customer. Key role t

Reference

2025-118998

Expiry date

01/01/0001

Tulio Sanquiz

Author

Tulio Sanquiz
Tulio Sanquiz

Author

Tulio Sanquiz
Read more Shortlist Save this role
Read more Shortlist Save this role
View Jobs

Browse popular job categories below or search all jobs above