Clinical project manager Work, Jobs in Waddon, Gtl (with Salaries)

RWE Clinical Project Manager (FSP)
IQVIA —London
- Full-time
- Remote
- Bachelor's degree
- Leadership
- Time management
- Work from home
Patient Experience Project Manager
Central London Community Healthcare NHS Trust —London
- £66,274 - £73,496 a year
- Full-time
- Continuous improvement
- Rehabilitation centre
1d
Clinical Trials Manager
Neurocrine Bioscience —London
- Full-time
- Computer literacy
- Data analysis skills
- Master's degree
16h
Project and Change Manager
Bupa —London
- From £70,000 a year
- Full-time
- Agile
- Communication skills
- Annual leave
- Work from home
Quick apply
Clinical Coding Administrator
IQVIA —London
- Part-time
- Remote
- Databases
- Work from home
5d
Senior Clinical Project Manager (Renal, Obesity, MASH) - Global Study Leadership
IQVIA —London
- Full-time
- Remote
- Bachelor's degree
- Team management
- Leadership
- Work from home
12d
Specialist, Clinical Trials
Neurocrine Bioscience —London
- Full-time
- Computer literacy
- Data analysis skills
- Master's degree
16h
Project Manager
MEDIDATA —London
- Hybrid work
- Organisational skills
- In-person
- Communication skills
- Annual leave
Clinical Trial Monitor
University College London —London
- £43,981 - £52,586 a year
- Full-time
- Spanish
- No degree
- Travel
- Annual leave
- Employee assistance programme
14d
eClinical Project Manager (London)
Medpace, Inc. —London
- Full-time
- Bachelor's degree
- In-person
- Medical terminology
- Annual leave
- Work from home
Project Management Team Lead – Clinical Trials (f/m/d)
Clariness GmbH —London
- Full-time
- English
- Continuous improvement
- Team management
- Flexible schedule
Quick apply
Project Coordinator, Data Monitoring - Entry Level
Medpace, Inc. —London
- Full-time
- Microsoft Powerpoint
- Microsoft Word
- Bachelor's degree
- Annual leave
- Work from home
6d
eClinical Coordinator (London)
Medpace, Inc. —London
- Full-time
- Microsoft Word
- Software troubleshooting
- English
- Annual leave
- Work from home
Manager, Clinical Study Lead
Regeneron —Uxbridge
- Bachelor's degree
- Continuous improvement
- Travel
- Annual leave
Clinical Site Manager
Qureight Ltd —London
- Full-time
- Hybrid work
- Continuous improvement
- Organisational skills
- Time management
- Annual leave
- Life insurance
Quick apply
eClinical Coordinator (London, Entry Level)
Medpace, Inc. —London
- Full-time
- Microsoft Word
- Software troubleshooting
- English
- Annual leave
- Work from home
Clinical Data Manager II/Senior Clinical Data Manager
Precision Medicine Group —London
- Remote
- Microsoft Word
- English
- Bachelor's degree
Environmental Sustainability Project Manager
Moorfields Eye Hospital NHS Foundation Trust —London
- £66,274 - £73,496 a year
- Full-time
- Writing skills
- Master's degree
- Analysis skills
10h
Clinical Data Manager II/Senior Clinical Data Manager
Precision for Medicine —London
- Remote
- Microsoft Word
- English
- Bachelor's degree
Quick apply
Client Services Project Manager Packaging
Thermo Fisher Scientific —Horsham
- Full-time
- Computer literacy
- Travel
- Organisational skills
12d

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RWE Clinical Project Manager (FSP)

IQVIA -
London

Apply Now

Job details

Full-time

Benefits

Work from home

Qualifications

Healthcare research operations
Clinical research
Stakeholder collaboration
Stakeholder liaison
Project team management
Bachelor's degree
Partnership building
Risk management
Project schedule tracking
Multidisciplinary collaboration
Pharmaceutical industry setting experience
Leadership
Project management experience
Project progress tracking
Time management

Full job description

London, 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 one 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, inflammation, virology

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 waddon, gtl

RWE Clinical Project Manager (FSP)

Patient Experience Project Manager

Clinical Trials Manager

Project and Change Manager

Clinical Coding Administrator

Senior Clinical Project Manager (Renal, Obesity, MASH) - Global Study Leadership

Specialist, Clinical Trials

Project Manager

Clinical Trial Monitor

eClinical Project Manager (London)

Project Management Team Lead – Clinical Trials (f/m/d)

Project Coordinator, Data Monitoring - Entry Level

eClinical Coordinator (London)

Manager, Clinical Study Lead

Clinical Site Manager

eClinical Coordinator (London, Entry Level)

Clinical Data Manager II/Senior Clinical Data Manager

Environmental Sustainability Project Manager

Clinical Data Manager II/Senior Clinical Data Manager

Client Services Project Manager Packaging

I want to receive the latest job alerts for clinical project manager in waddon, gtl

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