Pharmaceutical sciences manager Work, Jobs in Uxbridge, Gtl (with Salaries)

eClinical Coordinator (London, Entry Level)
Medpace, Inc. —London
- Full-time
- Microsoft Word
- Microsoft Excel
- English
- Annual leave
Clinical Trials Programme Manager
ICR —Sutton
- From £50,825 a year
- Call to connect
- Hybrid work
- Laboratory experience
- No degree
Senior Scientific Engagement & Program Manager
Novartis —London
- £53,532.50 - £99,417.50 a year
- Full-time
- Hybrid work
- Doctoral degree
- English
- Master's degree
eClinical Coordinator (London)
Medpace, Inc. —London
- Full-time
- Microsoft Word
- Microsoft Excel
- English
- Annual leave
Associate Scientist, Analytical
MedPharm —Guildford
- Full-time
- Computer literacy
- Laboratory experience
- Microsoft Office
Quick apply
1d
eClinical Project Manager (London)
Medpace, Inc. —London
- Full-time
- Bachelor's degree
- Medical terminology
- Time management
- Annual leave
Constant Climate Regulatory Compliance Executive
IAG Cargo —Hounslow
- Hybrid work
- Microsoft Office
- Continuous improvement
- Communication skills
- Employee discount
- Gym membership
8d
Study Manager - 1 year FTC
Roche —Welwyn
- Hybrid work
- Bachelor's degree
Clinical Trials Manager
Gilead Sciences —London
- Full-time
- Management
- Doctoral degree
- Master's degree
Senior Manager, Patient Safety Scientist
Bristol-Myers Squibb —Uxbridge
- Full-time
- Hybrid work
- Doctoral degree
- Master's degree
- Analysis skills
8d
Medical Assessor - £75,585 - £84,840 p.a. + benefits
Medicines and Healthcare Products Regulatory Agency —London
- £75,585 - £84,840 a year
- Full-time
- Presentation skills
- Travel
- In-person
- Annual leave
- Sick pay
11d
Associate Pharmacovigilance Project Manager (Europe)
PrimeVigilance —London
- Full-time
- Remote
- English
- Project management
- Mentoring
Quick apply
Scientific Affairs Manager, UK - London
Rhythm Pharmaceuticals —London
- Full-time
- Doctoral degree
- Presentation skills
- Communication skills
Operations Associate
Incite —London
- Full-time
- Hybrid work
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Quick apply
2d
Clinical Document Management Learning Manager
Novartis —London
- £49,140 - £91,260 a year
- Full-time
- Hybrid work
- Bachelor's degree
- No degree
- Contracts
Senior Manager, PV Process Quality Lead
Bristol-Myers Squibb —Uxbridge
- Full-time
- Hybrid work
- Microsoft Office
- Bachelor's degree
- Travel
Executive Director, Global Patient Safety Sciences Delivery
Regeneron —Uxbridge
- Management
- Doctoral degree
- Master's degree
- Annual leave
Pharmacovigilance & Medical Affairs Manager
Zentiva Group, a.s. —Guildford
- Full-time
- Organisational skills
- Leadership
Health & Safety Manager
Medik8 —Aylesbury
- £50,000 - £70,000 a year
- Hybrid work
- Google Suite
- Analysis skills
- IT
- Employee discount
Quick apply
Quality Assessor - £60,778 - £68,422 p.a. + benefits
Medicines and Healthcare Products Regulatory Agency —London
- £60,778 - £68,422 a year
- Full-time
- Doctoral degree
- Marketing
- Presentation skills
- Annual leave
- Sick pay
1d

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eClinical Coordinator (London, Entry Level)

Medpace, Inc. -
London

Apply Now

Job details

Full-time

Benefits

Annual leave
Company events

Qualifications

Microsoft Word
Microsoft Excel
Mathematics
English
Bachelor's degree
Communication skills

Full job description

Job Summary :

Our corporate activities are growing rapidly, and we are currently seeking a full-time, office-based eClinical Coordinator to join our Data Management team in Central London. The eClinical Coordinator at Medpace is a crucial component of the clinical trial process. By working with the eClinical Project Manager and other team members, these professionals ensure the accuracy of data reported by patients for clinical studies.

At Medpace, eClinical 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 :

Participate as part of a team on various project(s).
Work with vendors to ensure patient forms meet their respective electronic requirements.
Partner with Sponsors to develop application requirements for each unique study.
Assist in the creation and maintenance of metric reports and study specific documents.
Assist Clinical Db Programmers with configuring and testing applications.
Troubleshoot issues with applications by working with sites/sponsors.
Report compliance metrics to Sponsors.

Qualifications :

Bachelor's degree in Life Sciences or Mathematics
Strong attention to detail
Excellent working knowledge of Microsoft Excel and Word
Solid oral and written English Language communication skills

Training is available for entry-level candidates.

Medpace Overview :

Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV 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 its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 6,000 people across 40+ countries.

Why Medpace? :

People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today.

The work we’ve done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future.

Medpace Perks

Flexible work environment
Competitive compensation and benefits package
Competitive PTO packages
Structured career paths with opportunities for professional growth
Company-sponsored employee appreciation events
Employee health and wellness initiatives

Awards

Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024
Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility

What to Expect Next

A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.

Apply Now

Refine Your Search

pharmaceutical sciences manager jobs in uxbridge, gtl

eClinical Coordinator (London, Entry Level)

Clinical Trials Programme Manager

Senior Scientific Engagement & Program Manager

eClinical Coordinator (London)

Associate Scientist, Analytical

eClinical Project Manager (London)

Constant Climate Regulatory Compliance Executive

Study Manager - 1 year FTC

Clinical Trials Manager

Senior Manager, Patient Safety Scientist

Medical Assessor - £75,585 - £84,840 p.a. + benefits

Associate Pharmacovigilance Project Manager (Europe)

Scientific Affairs Manager, UK - London

Operations Associate

Clinical Document Management Learning Manager

Senior Manager, PV Process Quality Lead

Executive Director, Global Patient Safety Sciences Delivery

Pharmacovigilance & Medical Affairs Manager

Health & Safety Manager

Quality Assessor - £60,778 - £68,422 p.a. + benefits

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