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

RWE Senior/ Clinical Project Manager (FSP)
IQVIA —Reading
- Project management
- Bachelor's degree
- Continuous improvement
Clinical Project Manager I
Perspectum —Oxford
- £33,000 - £45,000 a year
- Full-time
- Project management
- Communication skills
Quick apply
Clinical Supplies Project Manager
ICON Plc —Reading
- Full-time
- Management
- Project management
- Bachelor's degree
- Employee assistance programme
2d
Sr. Clinical Project Manager (Europe)
Allucent —Bracknell
- Hybrid work
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
- Flexible schedule
- Referral programme
Quick apply
Clinical Trial Manager - Project Lead
ICON Plc —Reading
- Full-time
- Oracle
- Management
- Project management
- Employee assistance programme
5d
Project Manager I, IDEA
ICON Plc —Reading
- Full-time
- Project management
- Bachelor's degree
- Communication skills
- Employee assistance programme
7d
Research Assistant - Centralised National Virtual Clinic
University of Oxford —Oxford
- £35,681 - £41,636 a year
- Remote
- Psychology
- Organisational skills
- Annual leave
7d
Project Manager / Senior Project Manager - Life Sciences
Geo Language Services —Guildford
- Full-time
- SQL
- Organisational skills
- IT
Quick apply
NPI Project Manager
Siemens Healthineers —Oxford
- Full-time
- PMP
- Engineering
- Project management
- Annual leave
5d
Senior Study Startup Specialist
PSI CRO —Oxford
- Full-time
- Hybrid work
- English
- Bachelor's degree
- Organisational skills
Quick apply
Clinical Research Administator
University of Oxford —Oxford
- £32,108 - £40,514 a year
- Full-time
- Oracle
- Administrative experience
- Organisational skills
14d
Senior Clinical Data Manager - sponsor dedicated - oncology
Fortrea —Maidenhead
- Full-time
- Remote
- Presentation skills
- Mentoring
- Leadership
Trial Manager
University of Oxford —Oxford
- £39,424 - £47,779 a year
- Part-time
- Project management
- Annual leave
1d
Senior Clinical Programmer I
Allucent —Bracknell
- Full-time
- Hybrid work
- Computer Science
- Bachelor's degree
- Flexible schedule
- Referral programme
Quick apply
Senior Site Activation Coordinator
IQVIA —Reading
- Hybrid work
9d
Principal Investigator
Velocity Clinical Research, Inc. —High Wycombe
- Full-time
- Travel
Quick apply
Research Facilitator
Surrey and Borders Partnership NHS Foundation Trust —Chertsey
- £29,812 - £32,715 a year
- Full-time
- Free parking
5d
Senior Technical Designer - Medidata RAVE certified
Fortrea —Maidenhead
- Full-time
- Remote
- English
- Communication skills
- Time management

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Clinical Project Manager I
Perspectum —Oxford
Coordinating project activities and timelines to support successful project delivery. As a Clinical Project Manager I, you will support the delivery of clinical…
£33,000 - £45,000 a year
Quick apply
RWE Senior/ Clinical Project Manager (FSP)
IQVIA —Reading
Lead project vendor management related activities and communications per project requirements. In this role, the clinical project manager will be responsible…

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clinical project manager jobs near calcot, brk

RWE Senior/ Clinical Project Manager (FSP)

IQVIA -
Reading

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Job details

Qualifications

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

Full job description

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.

Apply Now

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clinical project manager jobs in calcot, brk

RWE Senior/ Clinical Project Manager (FSP)

Clinical Project Manager I

Clinical Supplies Project Manager

Sr. Clinical Project Manager (Europe)

Clinical Trial Manager - Project Lead

Project Manager I, IDEA

Research Assistant - Centralised National Virtual Clinic

Project Manager / Senior Project Manager - Life Sciences

NPI Project Manager

Senior Study Startup Specialist

Clinical Research Administator

Senior Clinical Data Manager - sponsor dedicated - oncology

Trial Manager

Senior Clinical Programmer I

Senior Site Activation Coordinator

Principal Investigator

Research Facilitator

Senior Technical Designer - Medidata RAVE certified

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