Regulatory project manager Work, Jobs in Burnham, Brk (with Salaries)

Project Coordinator, Data Monitoring - Entry Level
Medpace, Inc. —London
- Full-time
- Microsoft Powerpoint
- Microsoft Word
- Bachelor's degree
- Annual leave
- Work from home
Knowledge Manager (Communities & Innovation)/ Knowledge Communities Manager
Sisk —St Albans
- Full-time
- Organisational skills
- Business
- Communication skills
- Annual leave
Brand Manager
Bunzl UK & Ireland Portfolio Brands —Slough
- £40,000 - £60,000 a year
- Full-time
- Quality control
- SharePoint
- In-person
Quick apply
eClinical Coordinator (London, Entry Level)
Medpace, Inc. —London
- Full-time
- Microsoft Word
- Software troubleshooting
- English
- Annual leave
- Work from home
Head of Training
LRG —Camberley
- Hybrid work
- Project management
- Team management
- Organisational skills
Quick apply
Study Start Up Manager
Fortrea —Maidenhead
- Full-time
- Remote
- English
- Bachelor's degree
11d
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
Project Assistant - Clinical Safety
Medpace, Inc. —London
- Full-time
- English
- Administrative experience
- Organisational skills
- Annual leave
- Work from home
5d
Sustainability Transformation Manager
Centrica —Windsor
- Computer literacy
- Data analysis skills
- Analysis skills
9d
Bid and Project Manager
Ultra Intelligence & Communications —Maidenhead
- Full-time
- Hybrid work
- Leadership
- Communication skills
- Flexible schedule
Medical Affairs Coordinator
Servier —Slough
- Microsoft Office
- Databases
- Administrative experience
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
Regulatory Compliance Executive (Constant Climate)
IAG Cargo —Hounslow
- Hybrid work
- Microsoft Office
- Continuous improvement
- Communication skills
- Employee discount
- Gym membership
Associate Clinical Project Manager - Sponsor Dedicated
IQVIA —Reading
- Full-time
- Remote
- Microsoft Powerpoint
- Microsoft Word
- Leadership
- Work from home
Senior Clinical Data Manager - sponsor dedicated - oncology
Fortrea —Maidenhead
- Full-time
- Remote
- Presentation skills
- Mentoring
- Leadership
Associate Brand Manager - Abbott Marketing UK & I
Abbott Laboratories —Maidenhead
- Full-time
- Marketing
- Bachelor's degree
- Organisational skills
Manager, International Commercial Growth Projects
Energizer —High Wycombe
- £59,100 - £110,200 a year
- Full-time
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Quick apply
Junior Brand Innovation Manager
SC Johnson Lifestyle Brands —Frimley
- Full-time
- Analysis skills
- Bachelor's degree
- Continuous improvement
Quality Assurance & Regulatory Affairs Executive - Maternity Cover
TensCare Ltd —Epsom
- £35,000 - £42,500 a year
- Temporary
- Hybrid work
- Bachelor's degree
- Continuous improvement
- Team management
- Profit sharing
- Work from home
Quick apply
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
6d

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regulatory project manager jobs near burnham, brk

Project Coordinator, Data Monitoring - Entry Level

Medpace, Inc. -
London

Apply Now

Job details

Full-time

Benefits

Annual leave
Work from home
Company events

Qualifications

Microsoft Powerpoint
Microsoft Word
Meeting coordination
Clinical research
Stakeholder collaboration
Project coordination
Bachelor's degree
Multidisciplinary collaboration
Medical terminology
Communication skills

Full job description

Job Summary :

Our corporate activities are growing rapidly, and we are currently seeking a full-time, office-based Entry Level Project Coordinator to join our Global Internal Data Monitoring 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.

At Medpace, Project Coordinators go through an extensive onboarding and training process, which prepares them to become experts in their field. 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 :

Partner with the Independent Data Monitoring Manager to identify and contract independent physicians and industry experts to assemble Data Monitoring Committees (DMCs) to review of safety and efficacy data for ongoing trials
Act as a liaison between Clinical Operations, Sponsors, and DMC and SAC members
Provide administrative, logistical, and coordinating support for DMCs (including scheduling meetings, distributing unblinded data, and documenting decisions and outcomes)
Assist in the development and maintenance of study specific documents describing DMC processes and procedures
Maintain the study blind and handle unblinded materials with discretion to ensure confidentiality

Qualifications :

Bachelor's degree in life science or health related field
General knowledge of medical terminology and drug development process
Excellent written and verbal communication skills
Proficient knowledge of Microsoft Word, Excel, and PowerPoint

TRAVEL: None

Training is available for entry-level candidates.

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

regulatory project manager jobs in burnham, brk

Project Coordinator, Data Monitoring - Entry Level

Knowledge Manager (Communities & Innovation)/ Knowledge Communities Manager

Brand Manager

eClinical Coordinator (London, Entry Level)

Head of Training

Study Start Up Manager

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

Project Assistant - Clinical Safety

Sustainability Transformation Manager

Bid and Project Manager

Medical Affairs Coordinator

Sr. Clinical Data Manager (Netherlands, United Kingdom)

Regulatory Compliance Executive (Constant Climate)

Associate Clinical Project Manager - Sponsor Dedicated

Senior Clinical Data Manager - sponsor dedicated - oncology

Associate Brand Manager - Abbott Marketing UK & I

Manager, International Commercial Growth Projects

Junior Brand Innovation Manager

Quality Assurance & Regulatory Affairs Executive - Maternity Cover

Portfolio Manager, Imperial Clinical Trials Unit (Maternity Cover)

I want to receive the latest job alerts for regulatory project manager in burnham, brk

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