Clinical study manager Work, Jobs in Maidenhead, Brk (with Salaries)

Senior Clinical Data Manager - sponsor dedicated - oncology
Fortrea —Maidenhead
- Full-time
- Remote
- Presentation skills
- Mentoring
- Leadership
Senior Manager Medical Information
Vertex Pharmaceuticals —Paddington
- Full-time
- Remote
- Analysis skills
- Bachelor's degree
- In-person
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
3h
Connected Devices - Primary analyst, Spirometry
IQVIA —Reading
- Full-time
- Remote
- Computer literacy
- Work from home
Senior Manager, Clinical Data Management
Bristol-Myers Squibb —Uxbridge
- Full-time
- Hybrid work
- PMP
- Project management
- Presentation skills
Clinical Biospecimen Scientist - Single Sponsor Dedicated
IQVIA —Reading
- Full-time
- Remote
- Bachelor's degree
- Work from home
Senior Clinical Technology Specialist
IQVIA —Reading
- Full-time
- Remote
- Analysis skills
- Bachelor's degree
- SharePoint
- Work from home
Associate Director Quality - Client Dedicated ( Regional Clinical Compliance Lead)
IQVIA —Reading
- Full-time
- Remote
- Management
- English
- Microsoft Office
- Work from home
6d
Sr. Clinical Project Manager (Europe)
Allucent —Bracknell
- Hybrid work
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
- Flexible schedule
- Referral programme
Quick apply
Medical Strategy Lead, Oncology (Home-Based)
IQVIA —Reading
- Full-time
- Remote
- Microsoft Outlook
- English
- Business development
- Work from home
Clinical Trials Administrator x2
Imperial College London —White City
- £41,005 - £45,616 a year
- Part-time
- Administrative experience
5d
Patient & Site Engagement Operations Manager - Sponsor Dedicated (m/w/d)
IQVIA —Reading
- Full-time
- Remote
- Microsoft Word
- Microsoft Excel
- Data analysis skills
- Work from home
Local Study Associate Director
IQVIA —Reading
- Full-time
- Remote
- Patient monitoring
- English
- Project management
- Work from home
13d
Sr. CRA 1 - Single Sponsor Dedicated
IQVIA —Reading
- Full-time
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Clinical Trial Manager
ICON Plc —Reading
- Full-time
- Employee assistance programme
4d
CRA 2 - Single Sponsor Dedicated
IQVIA —Reading
- Full-time
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Associate Country Clinical Quality Manager
Fortrea —Maidenhead
- Full-time
- Analysis skills
- Bachelor's degree
Business Development Manager – Medical Affairs Solutions (IQVIA Pharma Review)
IQVIA —Reading
- Full-time
- Hybrid work
- Business development
- AI
- Communication skills
Marketing Manager: Patient Monitoring and Digital Solutions
Dräger UK & Ireland —Hemel Hempstead
- Hybrid work
- Master's degree
- Product management
- Travel
12d
Medical Writing Manager – Patient Centered Solutions, Strategic & Scientific Research
IQVIA —Reading
- Full-time
- Hybrid work
- Microsoft Office
- Bachelor's degree
- Medical terminology

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clinical study manager jobs near maidenhead, brk

Senior Clinical Data Manager - sponsor dedicated - oncology

Fortrea -
Maidenhead

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Job details

Full-time

Benefits

Company pension

Qualifications

Presentation skills
Data management
Mentoring
Leadership
Communication skills

Full job description

Senior Clinical Data Manager – FSP / oncology experience

The Senior Clinical Data Manager role is a great opportunity to work within our sponsor dedicated department and have this unique relationship with a sponsor. You will be responsible for the full cycle of Clinical Data Management queries, from being in full leadership of your own studies and being the main point of contact with the client, to the most hands-on tasks such as creating eCRFs, cleaning data and performing independently set-up to close-outs duties. You will cooperate in a highly collaborative environment with other Clinical Data Managers, Data Coordinators, Statistical Programmers and others.

What you can expect from us

Office based or home based anywhere in the listed countries
Exposure to high profile global studies with
Highly competitive compensation packages, including various local benefits such as pension contributions, complimentary health insurance plans, remote working allowances etc.
A genuine work life balance
Flexibility in working hours
A thorough onboarding with support from your personal mentor

What you will do

Provides CDM leadership for one or more assigned projects or indications dependent on size and scale of the project.
Lead studies including (but not limited to) a combination of healthy volunteer and patient populations, multi-site, complex protocol design, strong client management required or reduced timelines.
Demonstrates leadership and operational expertise in the strategic planning and delivery of CDM deliverables at program and/or project level.
Management and oversight of vendor contracts, resourcing and budget management and oversight of vendor performance for assigned programs, and projects
Communicates and negotiates effectively with all other Program level team members. Primary point of contact for Clinical Data Management (CDM)
Provide oversight and expertise of external service providers or in-house teams to deliver quality data with compliance to study model procedures and standards;
Responsible for proactive risk management and issue resolution/escalation connected to Clinical Data Management improvement or technology
Develops an understanding of CDASH and SDTM or other recognized industry standards and impact to programming team to ensure consistency of program level standards.

Your profile

University/college degree (life science, pharmacy or related subject preferred)

8 years of combined early or late-stage DM experience with minimum 2 years of direct sponsor management and at least 2 years technical mentoring experience.
Extensive experience in clinical data management and experience leading studies in a CRO/Pharma setting.
Understanding of RECIST criteria.
Excellent oral and written communication and presentation skills.
In depth knowledge of clinical trial process and data management, clinical operations, biometrics, quality management, and systems applications to support operations.
Working knowledge of the relationship and regulatory obligation of the CRO industry with pharmaceutical / biotechnological companies.

Fortrea is actively seeking motivated problem-solvers and creative thinkers who share our passion for overcoming barriers in clinical trials. Our unwavering commitment is to revolutionize the development process, ensuring the swift delivery of life-changing ideas and therapies to patients in need. Join our exceptional team and embrace a collaborative workspace where personal growth is nurtured, enabling you to make a meaningful global impact. For more information about Fortrea, visit www.fortrea.com .

Fortrea is proud to be an Equal Opportunity Employer:

As an EOE/AA employer, Fortrea strives for diversity and inclusion in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications of the individual and do not discriminate based upon race, religion, color, national origin, gender (including pregnancy or other medical conditions/needs), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. We encourage all to apply.

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Refine Your Search

clinical study manager jobs in maidenhead, brk

Senior Clinical Data Manager - sponsor dedicated - oncology

Senior Manager Medical Information

Senior Manager, Clinical Operations - FSP Resource & Vendor Management

Connected Devices - Primary analyst, Spirometry

Senior Manager, Clinical Data Management

Clinical Biospecimen Scientist - Single Sponsor Dedicated

Senior Clinical Technology Specialist

Associate Director Quality - Client Dedicated ( Regional Clinical Compliance Lead)

Sr. Clinical Project Manager (Europe)

Medical Strategy Lead, Oncology (Home-Based)

Clinical Trials Administrator x2

Patient & Site Engagement Operations Manager - Sponsor Dedicated (m/w/d)

Local Study Associate Director

Sr. CRA 1 - Single Sponsor Dedicated

Clinical Trial Manager

CRA 2 - Single Sponsor Dedicated

Associate Country Clinical Quality Manager

Business Development Manager – Medical Affairs Solutions (IQVIA Pharma Review)

Marketing Manager: Patient Monitoring and Digital Solutions

Medical Writing Manager – Patient Centered Solutions, Strategic & Scientific Research

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