JUMP TO CONTENT

Senior Pharmacovigilance Project Manager

  1. Blue Bell
JR124029
  1. Pharmacovigilance & Patient Safety
  2. ICON Full Service & Corporate Support
  3. Hybrid: Office/Remote

About the role

Senior Pharmacovigilance Project Manager- Blue Bell, PA- Remote

ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.

ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organisations.
With our patients at the centre of all that we do, we help to accelerate the development of drugs and devices that save lives and improve quality of life.
Our people are our greatest strength, are at the core of our culture, and the driving force behind our success. ICON people have a mission to succeed and a passion that ensures what we do, we do well.

We are currently seeking a Senior Pharmacovigilance Project Manager The Senior Pharmacovigilance Project Manager (PM) manages assigned projects that may range from simple to complex or portfolio and span across business units or functional areas. providing valuable insight into how areas impact one another.

Duties include:

Primary Customer Contact/Leadership

  • Act as the primary project manager for a portfolio of Pharmacovigilance projects, ensuring expectations are met. Serve as the primary liaison between the client and project team on matters of time, scope, cost, quality, and resources.

  • Provide leadership and mentoring to the project team, ensuring deliverables and timelines are met.

  • Lead cross-functional teams, vendors, and third parties with some supervision.

  • Collaborate with functional leads to optimize performance and manage team feedback.

  • Monitor compliance with regulatory, training, and budget requirements.

  • For complex projects, define success criteria, manage communication, and track deliverables to resolve issues and dependencies.

  • Manage department initiatives or assume the role of Director of Project Delivery for smaller projects as needed.

Communication

  • Lead client and internal meetings, approving agendas and minutes.

  • Present project status during internal reviews and financial meetings.

  • Serve as a subject matter expert (SME) for Pharmacovigilance proposals and lead bid defense processes.

  • Contribute to the development of practices and tools to drive process improvements.

  • Stay current on industry technologies, methods, and best practices.

Delivery

  • Manage project delivery per contract, ensuring on-time and on-budget completion.

  • Develop and manage the Project Management Plan throughout the project lifecycle.

  • Oversee project plans, task prioritization, troubleshooting, and contingency planning to ensure timely, high-quality delivery.

  • Prepare status reports for clients and leadership.

Finance

  • Oversee project budgets, resource allocation, and invoice approvals.

  • Identify, negotiate, and execute contract modifications.

  • Conduct in-depth analysis of timelines and financials for senior management and clients.

To be successful in the role, you will have:

  • A minimum of 6 years of experience working in pharmacovigilance as a project manager

  • Experience working for a CRO or Pharmaceutical company

  • Bachelor's Degree

  • Strong Communications skills


Benefits of Working in ICON:
Our success depends on the knowledge, capabilities and quality of our people. That’s why we are committed to developing our employees in a continuous learning culture – one where we challenge you with engaging work and where every experience adds to your professional development.

At ICON, our focus is to provide you with a comprehensive and competitive total reward package that comprises, not only an excellent level of base pay, but also a wide range of variable pay and recognition programs. In addition, our best in class employee benefits, supportive policies and wellbeing initiatives are tailored to support you and your family at all stages of your career - both now, and into the future.

ICON, including subsidiaries, is an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.

If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know through the form below.

#LI-MN1

#LI-Remote

What ICON can offer you:
Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent.

In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.

Our benefits examples include:

  • Various annual leave entitlements
  • A range of health insurance offerings to suit you and your family’s needs.
  • Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
  • Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family’s well-being.
  • Life assurance
  • Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others.

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

ICON, including subsidiaries, is an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, colour, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.

If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here

Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles.

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

List #1

Day in the life

gloved hand holding pipette and dropping a solution into test tubes
What is the purpose of a pharmacovigilance team in clinical research?

Teaser label

Inside ICON

Content type

Blogs

Publish date

02/17/2023

Summary

Clinical research is the backbone of the medical industry. Without it, it would be impossible for drugs and medical treatments to prove compliance and become approved for market sale. Drug safety

Teaser label

Now more than ever, it's important that we understand the value of pharmacovigilance

Read more
A picture of a pipette next to some drugs
What does a Drug Safety Associate (DSA) do?

Teaser label

Inside ICON

Content type

Blogs

Publish date

09/29/2022

Summary

A Drug Safety Associate is responsible for assessing the safety of pharmaceuticals drugs once they’re on the market. Using standardised guidelines, they determine whether the medication causes any adv

Teaser label

A Drug Safety Associate is responsible for assessing the safety of pharmaceuticals drugs once they’re on the market.

Read more
A picture of a scientist
How to write an outstanding CV for a life sciences job

Teaser label

Career Progression

Content type

Blogs

Publish date

02/28/2022

Summary

Around 268,000 people are employed by the UK life sciences industry and as one of the fastest-growing sectors, this number is expected to continue rising. Life sciences is a flourishing job market,

Teaser label

Learn expert tips on crafting an outstanding CV for life sciences jobs, from highlighting relevant skills and experience to tailoring your resume.

Read more
View all

Similar jobs at ICON

Senior Pharmacovigilance Project Manager

Salary

Location

Poland, Warsaw

Location

Sofia

Warsaw

Remote Working

Hybrid: Office/Remote

Business Area

ICON Full Service & Corporate Support

Job Categories

Pharmacovigilance & Patient Safety

Job Type

Permanent

Description

Senior Pharmacovigilance Project Manager -The role:Ensures that Standard Operating Procedures (SOPs), policies and guidelines are adhered to at the project level. Ensure assignment of project specific

Reference

JR124492

Expiry date

01/01/0001

Maya Katsarska Read more Shortlist Save this role
Pharmacovigilance Reporting Specialist

Salary

Location

Bulgaria, Sofia

Location

Sofia

Remote Working

Hybrid: Office/Remote

Business Area

ICON Full Service & Corporate Support

Job Categories

Drug Safety

Job Type

Permanent

Description

ICON plc is a world-leading healthcare intelligence and clinical research organization. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotech

Reference

JR124366

Expiry date

01/01/0001

Sophie Bingham Read more Shortlist Save this role
Pharmacovigilance Specialist

Salary

Location

India, Chennai

Location

Chennai

Remote Working

Office Based

Business Area

ICON Full Service & Corporate Support

Job Categories

Pharmacovigilance & Patient Safety

Job Type

Permanent

Description

Ensures accuracy and consistency of safety data processing from receipt from various sources to final output (e.g. reports, listings, data export) • Conducts and participates in review and quality con

Reference

JR124493

Expiry date

01/01/0001

Archana Bakkiyarajan Read more Shortlist Save this role
Clinical Research Physician, office based - Madrid, Spain

Salary

Location

Spain, Madrid

Location

Madrid

Remote Working

Office Based

Business Area

ICON Full Service & Corporate Support

Job Categories

Physician

Job Type

Permanent

Description

Clinical Research Physician Alcobendas, Madrid, Spain - Part-time, 3 days a week ONSITEAre you looking for an outstanding opportunity to develop your career with a fast growing leading edge Clinical r

Reference

JR124306

Expiry date

01/01/0001

Caroline Lock

Author

Caroline Lock
Read more Shortlist Save this role
Senior Pharmacovigilance Reporting Associate

Salary

Location

Brazil, Sao Paulo

Location

Sao Paulo

Remote Working

Office Based

Business Area

ICON Full Service & Corporate Support

Job Categories

Drug Safety

Job Type

Permanent

Description

The role:•    Serve as safety reporting or safety reporting intelligence processor and/or lead for multiple safety reporting or safety reporting intelligence stand-alone projects, providing management

Reference

JR124920

Expiry date

01/01/0001

Florencia Pistolesi Read more Shortlist Save this role
Clinical Research Physician

Salary

Location

Taiwan, Taipei

Location

Taipei

Remote Working

Hybrid: Office/Remote

Business Area

ICON Full Service & Corporate Support

Job Categories

Physician

Job Type

Permanent

Description

Job Description Summary• To aid in recruiting and screening healthy volunteers and patients for clinical trials. • To provide medical support for the conduct of studies. • To be responsible for the sa

Reference

JR125050

Expiry date

01/01/0001

Candice Wang

Author

Candice Wang
Read more Shortlist Save this role

Browse popular job categories below or search all jobs above