Clinical study manager Work, Jobs in Stanmore, Gtl (with Salaries)

Senior Manager Clinical Data Management Study Lead
Regeneron —Uxbridge
- £134,400 - £219,200 a year
- Management
- Bachelor's degree
- Annual leave
Lead Clinician for ADHD Children and Young People (CYP) Services
CareADHD —Canary Wharf
- £70,000 - £75,000 a year
- Hybrid work
- Supervising experience
- Leadership
- Communication skills
Quick apply
Head of CS - Under 18s Services
CareADHD —Canary Wharf
- £55,000 - £60,000 a year
- Hybrid work
- Sales
- Leadership
Quick apply
Senior Clinical Study Manager
Convatec —London
- Full-time
- Remote
- Management
- Up to 50% travel
- Bachelor's degree
Senior Manager Medical Information
Vertex Pharmaceuticals —Paddington
- Full-time
- Remote
- Analysis skills
- Bachelor's degree
- In-person
10d
Study Manager, Clinical Operations
Orchard Therapeutics —London
- Full-time
- Hybrid work
- Doctoral degree
- English
- Project management
Quick apply
Principal Clinical Research Specialist
Medtronic —Watford
- £64,800 - £97,200 a year
- Full-time
- Travel
- Organisational skills
- Communication skills
Sr. Clinical Project Manager (Europe)
Allucent —Bracknell
- Hybrid work
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
- Flexible schedule
- Referral programme
Quick apply
Clinical Research Project Manager (Part-Time, Maternity Cover)
Mitra Bio —London
- Part-time
- Travel
Clinical Trials Manager
Gilead Sciences —Uxbridge
- Full-time
- Hybrid work
- Travel
- Organisational skills
- Communication skills
Manager, Regulatory Clinical Trial Authorization (CTA)
CSL Behring —Maidenhead
- Full-time
- Customer service
- Computer literacy
- English
Quality Assurance Project Manager - GCP (with GMP awareness)
Ellipses Pharma —London
- Project management
- Travel
- Communication skills
5d
Single Sponsor Clinical Trial Manager (previous trial management exp needed (3 days a week in Uxbridge)
サイネオス・ヘルス —London
- Bachelor's degree
- Contracts
- Communication skills
Clinical Trial Associate Manager
Galderma —London
- Hybrid work
- Project management
- Bachelor's degree
- Leadership
GCP Compliance Manager - Clinical Programs & Trials
Novartis —London
- Full-time
- Hybrid work
- Engineering
- Communication skills
13d
Emergency Responder (West London)
St John Ambulance —West London
3d
Senior Clinical Trial Administrator
GE HEALTHCARE —Chalfont Saint Giles
- Travel
- Communication skills
7d
Study Manager - 1 year FTC
Roche —Welwyn
- Hybrid work
- Bachelor's degree
1d
Single Sponsor Clinical Project Manager II UK (Oncology) UK based (Days at client site, London)
Syneos - Clinical and Corporate - Prod —London
- Full-time
- Bachelor's degree
- Travel
- Organisational skills
Project Manager, Clinical Trials
Cogstate —London
- £55,000 - £60,000 a year
- Remote
- Computer Science
- Engineering
- Master's degree
- Annual leave
Quick apply

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clinical study manager jobs near stanmore, gtl

Senior Manager Clinical Data Management Study Lead

Regeneron -
Uxbridge

Apply Now

Job details

£134,400 - £219,200 a year

Benefits

Annual leave
Company pension

Qualifications

Management
Mathematics
Bachelor's degree
Data management

Full job description

Build our future together

At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Senior Manager, Clinical Data Management to join our Data Management [team/function], supporting our [region/business area]. In this role, you will oversee clinical data management studies and ensure high-quality, timely delivery of data management outputs while collaborating with clinical study teams, CROs, and external data vendors. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.

When & where:

Remote US

Discover your role:

Lead data management activities across studies from start-up to archiving
Serve as primary contact for study teams, CROs, vendors
Oversee data quality review, acceptance, and database lock processes
Manage data transfers, coding, and reconciliation across systems
Review and approve study documentation including data plans and specifications
Ensure inspection readiness and maintain compliant documentation in eTMF
You collaborate effectively across cross-functional and external teams
You prioritize multiple activities while maintaining strong attention to detail

This role requires:

Bachelor’s degree in Mathematics, Science, or related field
Minimum 8+ years of clinical data management experience in relevant industry
Demonstrated knowledge of regulations including 21 CFR Part 11 and ICH-GCP
Proven experience leading studies and data management teams
Strong understanding of data management processes and industry standards
Certified Clinical Data Manager (CCDM) certification
Experience with people management and team development

Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.

Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter.

Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.

As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.

For jobs in Canada: this posting is for an existing position.

Salary Range (annually)

$134,400.00 - $219,200.00

Apply Now

Refine Your Search

clinical study manager jobs in stanmore, gtl

Senior Manager Clinical Data Management Study Lead

Lead Clinician for ADHD Children and Young People (CYP) Services

Head of CS - Under 18s Services

Senior Clinical Study Manager

Senior Manager Medical Information

Study Manager, Clinical Operations

Principal Clinical Research Specialist

Sr. Clinical Project Manager (Europe)

Clinical Research Project Manager (Part-Time, Maternity Cover)

Clinical Trials Manager

Manager, Regulatory Clinical Trial Authorization (CTA)

Quality Assurance Project Manager - GCP (with GMP awareness)

Single Sponsor Clinical Trial Manager (previous trial management exp needed (3 days a week in Uxbridge)

Clinical Trial Associate Manager

GCP Compliance Manager - Clinical Programs & Trials

Emergency Responder (West London)

Senior Clinical Trial Administrator

Study Manager - 1 year FTC

Single Sponsor Clinical Project Manager II UK (Oncology) UK based (Days at client site, London)

Project Manager, Clinical Trials

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