Clinical study manager Work, Jobs in Southwark, Gtl (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
eClinical Coordinator (London, Entry Level)
Medpace, Inc. —London
- Full-time
- Microsoft Word
- Software troubleshooting
- English
- Annual leave
- Work from home
Clinical Study Specialist
Regeneron —Uxbridge
- Hybrid work
- Bachelor's degree
- SharePoint
- Annual leave
9d
Study Manager, Clinical Operations
Orchard Therapeutics —London
- Full-time
- Hybrid work
- Doctoral degree
- English
- Travel
Quick apply
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
Senior Clinical Project Manager (Renal, Obesity, MASH) - Global Study Leadership
IQVIA —London
- Full-time
- Remote
- Bachelor's degree
- Team management
- Leadership
- Work from home
Project Manager
University College London —London
- Full-time
- Remote
- PMP
- University
- Continuous improvement
- Annual leave
- Employee assistance programme
12d
Career Evening at Medpace London - Project Coordinator
Medpace, Inc. —London
- Full-time
- English
- Bachelor's degree
- Organisational skills
- Annual leave
- Work from home
6d
Junior Project Manager
M3EU —London
- Full-time
- Remote
- Writing skills
- Project management
- Bachelor's degree
- Annual leave
- Employee discount
Quick apply
14d
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
9d
Research Regulatory Facilitator
Imperial College London —White City
- £48,246 - £58,318 a year
- Full-time
- University
- Time management
- Annual leave
Regulatory Submissions (Study Start-up) Manager
Medpace, Inc. —London
- Full-time
- In-person
- Leadership
- Communication skills
- Annual leave
- Work from home
7d
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
Manager, Clinical Study Lead
Regeneron —Uxbridge
- Bachelor's degree
- Continuous improvement
- Travel
- Annual leave
Freelance Site Activation Specialist (Study Start-Up / Regulatory Submissions) – UK Remote
IQVIA —London
- Full-time
- Remote
- English
- Bachelor's degree
- Communication skills
- Work from home
1d
Global Medical Affairs Research Grant & Study Manager
Santen —St Albans
- £78,863 - £108,436 a year
- Full-time
- Hybrid work
- Nursing
- Doctoral degree
- English
Quick apply
Clinical Data Manager - FSP (Homebased - UK)
IQVIA —London
- Full-time
- Remote
- Bachelor's degree
- Quality control
- Work from home
12d
Clinical Support Specialist - 12 month FTC, Full-Time
hVIVO Services Limited —London
- Overtime
- Customer service
- Communication skills
- Annual leave
- Employee assistance programme
Clinical Research Nurse - 12 month FTC
hVIVO Services Limited —London
- Night shift
- Microsoft Word
- Nursing
- Mentoring
Clinical Genomics Scientific Administrator
The Royal Marsden NHS Foundation Trust —Sutton
- £33,262 - £36,027 a year
- Full-time
- Organisational skills
- Communication skills
5d

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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

clinical study manager jobs in southwark, gtl

Project Coordinator, Data Monitoring - Entry Level

eClinical Coordinator (London, Entry Level)

Clinical Study Specialist

Study Manager, Clinical Operations

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

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

Project Manager

Career Evening at Medpace London - Project Coordinator

Junior Project Manager

Portfolio Manager, Imperial Clinical Trials Unit (Maternity Cover)

Research Regulatory Facilitator

Regulatory Submissions (Study Start-up) Manager

Quality Assurance & Regulatory Affairs Executive - Maternity Cover

Manager, Clinical Study Lead

Freelance Site Activation Specialist (Study Start-Up / Regulatory Submissions) – UK Remote

Global Medical Affairs Research Grant & Study Manager

Clinical Data Manager - FSP (Homebased - UK)

Clinical Support Specialist - 12 month FTC, Full-Time

Clinical Research Nurse - 12 month FTC

Clinical Genomics Scientific Administrator

I want to receive the latest job alerts for clinical study manager in southwark, gtl

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