Clinical project manager Work, Jobs in Stratfield Mortimer, Brk (with Salaries)

RWE Senior/ Clinical Project Manager (FSP)
IQVIA —Reading
- Full-time
- Remote
- Project management
- Bachelor's degree
- Continuous improvement
- Work from home
Sr. Clinical Project Manager (Europe)
Allucent —Bracknell
- Hybrid work
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
- Flexible schedule
- Referral programme
Quick apply
Project Manager / Senior Project Manager - Life Sciences
Geo Language Services —Guildford
- Full-time
- SQL
- Organisational skills
- IT
Quick apply
Sr. CRA 1 - Site Management
IQVIA —Reading
- Full-time
- Remote
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
- Work from home
Project Manager, eCOA
IQVIA —Reading
- Full-time
- Remote
- PMP
- Public speaking
- English
- Work from home
Global Clinical Project Manager - Vendor Management Expert (home-based in Europe)
IQVIA —Reading
- Full-time
- Remote
- Laboratory experience
- Project management
- Communication skills
- Work from home
12d
ECOA Project Manager
ICON Plc —Reading
- Full-time
- Remote
- Management
- Project management
- Presentation skills
- Employee assistance programme
4d
Vendor Startup Manager IRT – Single Sponsor (home-based)
IQVIA —Reading
- Full-time
- Remote
- Continuous improvement
- Communication skills
- Work from home
Site Activation Specialist
IQVIA —Reading
- Full-time
- Remote
- Travel
- Contracts
- Negotiation
- Work from home
Local Study Associate Director
IQVIA —Reading
- Full-time
- Remote
- Patient monitoring
- English
- Project management
- Work from home
11d
Sr. CRA 1 - Single Sponsor Dedicated
IQVIA —Reading
- Full-time
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
RWE Alliance Manager (FSP)
IQVIA —Reading
- Full-time
- Remote
- Project management
- Bachelor's degree
- Continuous improvement
- Work from home
2d
CRA 2 - Single Sponsor Dedicated
IQVIA —Reading
- Full-time
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Patient & Site Engagement Operations Manager - Sponsor Dedicated (m/w/d)
IQVIA —Reading
- Full-time
- Remote
- Microsoft Word
- Microsoft Excel
- Data analysis skills
- Work from home
Senior Clinical Data Manager - sponsor dedicated - oncology
Fortrea —Maidenhead
- Full-time
- Remote
- Presentation skills
- Mentoring
- Leadership
Global Trial Manager, Late Phase Studies, Single-Sponsor Dedicated (home-based in Europe)
IQVIA —Reading
- Full-time
- Remote
- Organisational skills
- Communication skills
- Work from home
Clinical Registry Coordinator
ICON Plc —Reading
- Full-time
- Remote
- Microsoft Office
- Project management
- Bachelor's degree
- Employee assistance programme
3d
Senior Site Activation Coordinator
IQVIA —Reading
- Full-time
- Hybrid work
13d
Senior Clinical Programmer I
Allucent —Bracknell
- Full-time
- Hybrid work
- Computer Science
- Bachelor's degree
- Flexible schedule
- Referral programme
Quick apply
Senior Technical Designer - Medidata RAVE certified
Fortrea —Maidenhead
- Full-time
- Remote
- English
- Communication skills
- Time management

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clinical project manager jobs near stratfield mortimer, brk

RWE Senior/ Clinical Project Manager (FSP)

IQVIA -
Reading

Apply Now

Job details

Full-time

Benefits

Work from home

Qualifications

Clinical research
Project management
Bachelor's degree
Continuous improvement
IT
Leadership
Time management

Full job description

Reading, United Kingdom | Full time | Home-based | R1552795

Job Overview

IQVIA is hiring a clinical project manager to expand our dedicated Real World Evidence (RWE) FSP team, working fully within the environment of a prominent pharma company. In this role, the clinical project manager will be responsible for end-to-end project delivery of real-world observational studies within the oncology therapeutic area. It is important for this individual to have experience working in observational research across primary and secondary data collection study designs as well as leading clinical studies independently.

Who do you work with?

Epidemiologists, data science, and clinical leads to deliver project specific goals and timelines
Vendors to communicate status of deliverables and workflow
Program and business leads to manage full portfolio of projects

What are you great at?

Independently executing observational and real-world studies while balancing speed, quality, and cost
Leading cross-functional teams to achieve milestones and resolve study issues
Proactively identifying risks and implementing mitigation plans
Communicating clearly with stakeholders, including preparing and presenting project updates to leadership
Good understanding of project financials including experience managing, contractual obligations and implications
Driving operational excellence and strategic partnership with clients
Managing vendors effectively across different sourcing models (in-house, hybrid, outsourced)
Bringing clarity to complex or ambiguous situations and making informed decisions
Results-oriented approach to work towards delivery and output
Strong organizational, prioritization, and time management skills
Ability to operate effectively in a matrixed, fast-paced, and evolving environment

Your responsibilities may include:

Leading global, cross-functional observational study teams and owning delivery of contracted scope, timelines, and quality
Developing study documentation, including project management plans
Ensuring consistent use of study tools, training materials, and compliance with SOPs, policies, and procedures
Monitoring study progress and financial performance; supporting forecasting and change control as needed
Lead project vendor management related activities and communications per project requirements
Anticipating operational and quality risks, responding to issues raised by the project team and planning/implementing appropriate corrective or preventative actions
Generating project- or program-level metrics and reports for senior management
Capturing lessons learned and contributing to continuous improvement and best practices

Required knowledge, skills, and abilities

Bachelor's degree in life sciences or related field
Minimum 4-6 years of experience in project management and/or clinical operations within pharma, CRO, or RWE environment (or equivalent combination of education, training, and experience)
Demonstrated experience leading observational or real-world evidence studies
Strong understanding of RWE study designs and clinical research conduct and skill in applying applicable clinical research regulatory requirements
Experience with primary and secondary data study designs
Therapeutic area expertise desired (oncology)

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Where you'll work

Home-based

You’ll work remotely, with the flexibility to do your best work from home. Supported by collaborative tools and a global team, you’ll stay connected while enjoying the autonomy and balance that comes with a fully remote role.

Culture

Culture at IQVIA is built on a shared belief: that when people are empowered with better data, smarter technology and deeper expertise, they can change what’s possible for patients. Across every team and every corner of the globe, you’ll find colleagues who genuinely care — about the mission and about each other. That’s what makes this a place where people tend to stay, grow and do the best work of their careers.

Apply Now

Refine Your Search

clinical project manager jobs in stratfield mortimer, brk

RWE Senior/ Clinical Project Manager (FSP)

Sr. Clinical Project Manager (Europe)

Project Manager / Senior Project Manager - Life Sciences

Sr. CRA 1 - Site Management

Project Manager, eCOA

Global Clinical Project Manager - Vendor Management Expert (home-based in Europe)

ECOA Project Manager

Vendor Startup Manager IRT – Single Sponsor (home-based)

Site Activation Specialist

Local Study Associate Director

Sr. CRA 1 - Single Sponsor Dedicated

RWE Alliance Manager (FSP)

CRA 2 - Single Sponsor Dedicated

Patient & Site Engagement Operations Manager - Sponsor Dedicated (m/w/d)

Senior Clinical Data Manager - sponsor dedicated - oncology

Global Trial Manager, Late Phase Studies, Single-Sponsor Dedicated (home-based in Europe)

Clinical Registry Coordinator

Senior Site Activation Coordinator

Senior Clinical Programmer I

Senior Technical Designer - Medidata RAVE certified

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