Clinical trial manager Work, Jobs in Addlestone, Sry (with Salaries)

Project Assistant - Clinical Safety
Medpace, Inc. —London
- Full-time
- English
- Administrative experience
- Organisational skills
- Annual leave
- Work from home
11d
Project Coordinator, Data Monitoring - Entry Level
Medpace, Inc. —London
- Full-time
- Microsoft Powerpoint
- Microsoft Word
- Bachelor's degree
- Annual leave
- Work from home
Clinical Data Manager
Cancer Research UK —London
- £39,000 - £44,000 a year
- Full-time
- Remote
- Nursing
- Organisational skills
- Communication skills
8d
Single Sponsor Clinical Project Manager II (Virology) - 1-2 days in Uxbridge (offices moving to London in May26)
Syneos - Clinical and Corporate - Prod —London
- Full-time
- PMP
- Bachelor's degree
- Organisational skills
eClinical Coordinator (London, Entry Level)
Medpace, Inc. —London
- Full-time
- Microsoft Word
- Software troubleshooting
- English
- Annual leave
- Work from home
Clinical Research Associate I
Fortrea —Maidenhead
- Full-time
Medical Science Liaison, Lipids – North of England, Scotland & Northern Ireland
MSD —London
- Full-time
- Microsoft Office
- Project management
- Travel
Clinical Study Specialist
Regeneron —Uxbridge
- Hybrid work
- Bachelor's degree
- SharePoint
- Annual leave
12d
Portfolio Manager, Imperial Clinical Trials Unit (Maternity Cover)
Imperial College London —White City
- £59,808 - £71,793 a year
- Full-time
- Bachelor's degree
- Training & development
- Annual leave
12d
Associate Clinical Project Manager - Sponsor Dedicated
IQVIA —Reading
- Full-time
- Remote
- Microsoft Powerpoint
- Microsoft Word
- Leadership
- Work from home
Senior Manager, Clinical Operations - FSP Resource & Vendor Management
CSL Behring —Maidenhead
- £170,000 - £201,000 a year
- Full-time
- Master's degree
- Bachelor's degree
Senior Medical Writer (remote US-based)
Porterhouse Medical Group —Reading
- Remote
- Doctoral degree
- Research
- Master's degree
- Annual leave
Senior Clinical Data Manager - sponsor dedicated - oncology
Fortrea —Maidenhead
- Full-time
- Remote
- Presentation skills
- Mentoring
- Leadership
Research Assistant (My Voice)
University College London —London
- £39,807 - £41,833 a year
- Full-time
- Hybrid work
- Research
- Experience working with children
- Recruiting
- Annual leave
- Employee assistance programme
12d
Project Manager
University College London —London
- Full-time
- Remote
- PMP
- University
- Continuous improvement
- Annual leave
- Employee assistance programme
Senior Clinical Trial Case Manager
CSL Behring —Maidenhead
- Full-time
- Doctoral degree
- Master's degree
- Bachelor's degree
Sr. Clinical Data Manager (Netherlands, United Kingdom)
Allucent —Bracknell
- Full-time
- Hybrid work
- Microsoft Powerpoint
- Bachelor's degree
- Training & development
- Flexible schedule
- Referral programme
Quick apply
Client Services Associate Project Manager Packaging
Thermo Fisher Scientific —Horsham
- Full-time
- Microsoft Powerpoint
- Microsoft Word
- Computer literacy
10d
ECOA Project Manager
ICON Plc —Reading
- Full-time
- Remote
- Presentation skills
- Bachelor's degree
- Leadership
- Employee assistance programme
Local Study Associate Director
IQVIA —Reading
- Full-time
- Remote
- English
- Bachelor's degree
- No degree
- Work from home

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clinical trial manager jobs near addlestone, sry

Project Assistant - Clinical Safety

Medpace, Inc. -
London

Apply Now

Job details

Full-time
11 days ago

Benefits

Annual leave
Work from home
Company events

Qualifications

Administrative support experience
English
Microsoft Office Suite
Administrative experience
Organisational skills
Medical terminology
Communication skills
A Level
Project progress tracking

Full job description

Job Summary :

Our corporate activities are growing rapidly, and we are currently seeking a full-time, office-based Project Assistant to join our Clinical Safety team. This position will work on a team to accomplish tasks and projects that are instrumental to the company’s success. If you want an exciting career where you use your previous expertise and can develop and grow your career even further, then this is the opportunity for you.

Responsibilities :

Provide day to day project support to the clinical safety department.
Support safety coordinators and managers with follow-up on cases.
Manage and maintain main mailbox and assist with triage.
Create and maintain project-related trackers and status reports.
Assist with case processing activities as delegated.
Conduct quality control reviews of departmental documents.
Perform other tasks as needed.

Qualifications :

A-levels - desirable, GCSEs – requirement (English, Science and Maths grade 6 - 9/A - C).
Administrative experience is beneficial.
Excellent organizational and prioritization skills are needed.
Knowledge of Microsoft Office required.
Knowledge of medical terminology, and an interest in clinical trials/drug development – desirable.
Applicants should have great attention to detail and excellent oral and written communication skills in English.

Medpace Overview :

Medpace is a full-service clinical contract research organization (CRO) providing phase l-lV clinical development services to the biotechnology, pharmaceutical, and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through the advancement of clinical research. We leverage in-country regulatory and therapeutic expertise across all major therapeutic areas including oncology, cardiology, metabolic, endocrinology, central nervous system, and anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, we employ more than 6,500 people across 40+ countries.

Why Medpace? :

When you join Medpace, you become part of an innovative team that brings cutting-edge therapies to market while building a meaningful and rewarding career focused on scientific excellence and improving patient outcomes around the world through continuous learning and cross-functional collaboration.

Purpose-Driven Work

- Work alongside physicians, scientists, and industry-leading experts committed to advancing the global development of medical therapeutics through clinical research excellence

Collaborative Culture

- Contribute to an interactive team environment that empowers decision making, creative thinking, and continuous learning through open communication and mutual trust.
- Leadership throughout Medpace is both accessible and approachable

Continuous Growth & Development

- Office based environment with on-site mentors
- Defined career paths with clear advancement opportunities
- Industry renowned onboarding and training programs designed to accelerate professional development
- Ongoing training and continuous learning opportunities throughout your career
- An environment that encourages employees to influence change, contribute ideas, and grow quickly

Other Employee Benefits

- Competitive compensation programs that recognize and reward performance
- Comprehensive health, wellness, retirement, and PTO benefits
- Office based culture with occasional WFH that provides flexibility for eligible positions after training
- Company-sponsored social events

Please note benefits may vary based on country.

What to Expect Next

A Medpace team member will review your application and if your profile matches our current needs, you will be contacted for an interview. While we review all applications carefully, we are unable to respond to every applicant, and only candidates selected for interviews will be contacted.

Apply Now

Refine Your Search

clinical trial manager jobs in addlestone, sry

Project Assistant - Clinical Safety

Project Coordinator, Data Monitoring - Entry Level

Clinical Data Manager

Single Sponsor Clinical Project Manager II (Virology) - 1-2 days in Uxbridge (offices moving to London in May26)

eClinical Coordinator (London, Entry Level)

Clinical Research Associate I

Medical Science Liaison, Lipids – North of England, Scotland & Northern Ireland

Clinical Study Specialist

Portfolio Manager, Imperial Clinical Trials Unit (Maternity Cover)

Associate Clinical Project Manager - Sponsor Dedicated

Senior Manager, Clinical Operations - FSP Resource & Vendor Management

Senior Medical Writer (remote US-based)

Senior Clinical Data Manager - sponsor dedicated - oncology

Research Assistant (My Voice)

Project Manager

Senior Clinical Trial Case Manager

Sr. Clinical Data Manager (Netherlands, United Kingdom)

Client Services Associate Project Manager Packaging

ECOA Project Manager

Local Study Associate Director

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