Clinical monitoring lead Work, Jobs in Basingstoke, Ham (with Salaries)

Clinical Monitoring Lead
Biogen —Maidenhead
- Full-time
- Hybrid work
- Nursing
- Bachelor's degree
- Team management
6d
HHCS Facilities Lead
Hampshire Hospitals NHS Foundation Trust —Basingstoke
- £32,073 - £39,043 a year
- Full-time
- Continuous improvement
7d
Sr. Clinical Project Manager (Europe)
Allucent —Bracknell
- Hybrid work
- Microsoft Powerpoint
- Microsoft Word
- English
- Flexible schedule
- Referral programme
Quick apply
HCA (Health Care Assistant) / Health Care Support Worker
Mosaic Primary Care Network —Basingstoke
- £13.84 an hour
- Part-time
- Inventory control
- Microsoft Office
- Cleaning
Quick apply
2d
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
14d
Manager, Clinical Data Management
IQVIA —Reading
- Full-time
- Remote
- Databases
- Bachelor's degree
- Team management
- Work from home
7d
Senior Coach
ICE Creates —Reading
- £28,000 a year
- Weekend availability
- Hybrid work
- CRM software
- Management
- No degree
- Health & wellbeing programme
- Sick pay
Quick apply
1h
Pharmacy Team Lead
Montu UK —Wokingham
- £35,000 - £45,000 a year
- Weekend availability
- Computer literacy
- Continuous improvement
- Mentoring
- Free parking
Quick apply
23h
Sessions - Clinical Director: Ambulance, 111 and Urgent Care
NHS Surrey and Sussex ICB —Woking
- Part-time
- Research
- Continuous improvement
Site SSU Lead - UK/ROI (remote)
Fortrea —Maidenhead
- Full-time
- Remote
- Analysis skills
- Bachelor's degree
- Continuous improvement
Senior Benefits Risk Management Lead
Bayer —Reading
- £110,000 - £130,000 a year
- Full-time
- Hybrid work
- English
- Databases
- Continuous improvement
- Annual leave
- Employee discount
QA Specialist
MedPharm —Guildford
- Full-time
- Master's degree
- Bachelor's degree
- Continuous improvement
Quick apply
Clinical Director: MH, LD, Autism and Neurodivergence
NHS Surrey and Sussex ICB —Woking
- Part-time
- Research
- Continuous improvement
Local Study Associate Director
IQVIA —Reading
- Full-time
- Remote
- English
- Bachelor's degree
- No degree
- Work from home
Senior Clinical Pharmacist – 12 Month Fixed Term
Circle Health Group —Basingstoke
- Up to £54,325 a year
- Full-time
- Supervising experience
- Mentoring
- Training & development
- Employee discount
- Life insurance
Associate Director, Clinical Trial Disclosure & Transparency
CSL Behring —Maidenhead
- Full-time
- Hybrid work
- Bachelor's degree
- Continuous improvement
- Communication skills
9d
Senior CRA
Fortrea —Maidenhead
- Full-time
- Communication skills
Senior/ Medical Writer - FSP
IQVIA —Reading
- Full-time
- Hybrid work
- Microsoft Word
- Doctoral degree
- Master's degree
12d
Manager II, Clinical Operations FSO and FSP (UK/IRE)
Fortrea —Maidenhead
- Full-time
- Nursing
- Continuous improvement
- Leadership
7d
Health and Safety Advisor
Healthcare Partners Ltd —Guildford
- £41,956 - £50,524 a year
- Full-time
- Analysis skills
- Training & development
8d

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clinical monitoring lead jobs near basingstoke, ham

Clinical Monitoring Lead

Biogen -
Maidenhead

Apply Now

Job details

Full-time
6 days ago

Qualifications

Nursing
Clinical research
Stakeholder collaboration
Stakeholder liaison
Performance management
Bachelor's degree
Team management
Clinical compliance monitoring
Professional development mentoring
Multidisciplinary collaboration
Good Clinical Practice (GCP)
Training & development
Leadership
Communication skills
Good Clinical Practice (ICH-GCP) guidelines
FDA regulations

Full job description

About This Role:

As a Clinical Monitoring Lead, you will be at the forefront of ensuring high-quality trial execution and regulatory compliance within assigned studies. Your role is pivotal in leading the clinical monitoring function, providing direct oversight and operational leadership to Site Managers (SMs) and Clinical Trial Coordinators (CTCs). You will ensure effective monitoring of clinical sites, adherence to ICH-GCP and SOPs, and timely resolution of study issues. By supporting operational readiness for inspection, maintaining data integrity, and ensuring operational consistency across monitoring activities, you will contribute significantly to the success of our clinical trials. This position offers an opportunity to make a real-world impact by driving excellence in clinical monitoring and collaborating closely with Quality Assurance and other stakeholders.

What You’ll Do:

Lead and manage Site Managers in all aspects of site monitoring, including site selection, initiation, routine monitoring, and close-out.
Review monitoring visit reports and follow-up letters for accuracy, completeness, and compliance with protocol, SOPs, and regulatory requirements.
Ensure consistent application of risk-based and centralized monitoring strategies across studies.
Track and report on site performance, enrollment, data quality, and issue resolution.
Ensure timely and accurate documentation in the Trial Master File (TMF) and support audit and inspection readiness.
Partner with Quality Assurance to conduct root cause analyses and implement corrective and preventive actions (CAPAs).
Supervise, coach, and mentor Site Managers, conducting performance reviews and supporting professional development.
Deliver Site Manager training on protocol requirements, therapeutic area knowledge, and monitoring best practices.
Collaborate with CTDU, CTAU, and other stakeholders to align on trial execution operational strategies.
Act as a subject matter expert on monitoring execution for internal and external partners.
Complete trip report reviews in compliance with study plan timelines.
Identify and escalate site performance issues, conduct trend analysis, and ensure issue resolution per plan.
Perform accompanied site visits with site managers, as applicable, and attend sponsor meetings to discuss country/region startup progress, trends, and issue escalation.
Generate monitoring plans, site blinding and training plans, and trip report completion annotations.

Who You Are:

You are a proactive leader with a keen eye for detail and a passion for clinical research. Your ability to mentor and guide teams ensures that every study you oversee is conducted with precision and excellence. You thrive in a collaborative environment, where your communication skills foster strong relationships across the organization. Your adaptability allows you to manage multiple tasks efficiently, even amidst shifting priorities and tight timelines. With your strategic mindset, you drive performance and maintain high standards of compliance and quality in all monitoring activities.

Required Skills:

Bachelor’s degree in life sciences, nursing, pharmacy, or related field; advanced degree preferred.
Extensive clinical monitoring experience with a strong background as a Clinical Research Associate (CRA).
Proven experience in CRA management, mentoring, and monitoring oversight within a clinical research environment.
Strong understanding of ICH-GCP, FDA/EMA regulations, and global clinical trial guidelines.
Demonstrated experience in CRA performance management and inspection readiness.
Excellent organizational, leadership, and problem-solving skills.
Strong communication skills, both written and verbal.
Willingness to travel (25–40%, as required).
Ability to build relationships across the organization and operate effectively in a hybrid or remote environment.
Proven ability to manage multiple tasks of varying complexity within tight timelines and shifting priorities.
Strong leadership skills with the ability to influence and drive performance across clinical trial teams assigned.

Preferred Skills:

Advanced degree in life sciences or related field.
Experience with risk-based monitoring strategies.
Familiarity with electronic Trial Master File systems and clinical trial management systems.

Job Level: Management

Why Biogen?

We are a global team with a commitment to excellence, and a pioneering spirit. As a mid-sized biotechnology company, we provide the stability and resources of a well-established business while fostering an environment where individual contributions make a significant impact. Our team encompasses some of the most talented and passionate achievers who have unparalleled opportunities for learning, growth, and expanding their skills. Above all, we work together to deliver life-changing medicines, with every role playing a vital part in our mission. Caring Deeply. Achieving Excellence. Changing Lives.

At Biogen, we are committed to building on our culture of inclusion and belonging that reflects the communities where we operate and the patients we serve. We know that diverse backgrounds, cultures, and perspectives make us a stronger and more innovative company, and we are focused on building teams where every employee feels empowered and inspired. Read on to learn more about Biogen.

All qualified applicants will receive consideration for employment without regard to sex, gender identity or expression, sexual orientation, marital status, race, color, national origin, ancestry, ethnicity, religion, age, veteran status, disability, genetic information or any other basis protected by federal, state or local law. Biogen is an E-Verify Employer in the United States.

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Refine Your Search

clinical monitoring lead jobs in basingstoke, ham

Clinical Monitoring Lead

HHCS Facilities Lead

Sr. Clinical Project Manager (Europe)

HCA (Health Care Assistant) / Health Care Support Worker

Senior Manager, Clinical Operations - FSP Resource & Vendor Management

Manager, Clinical Data Management

Senior Coach

Pharmacy Team Lead

Sessions - Clinical Director: Ambulance, 111 and Urgent Care

Site SSU Lead - UK/ROI (remote)

Senior Benefits Risk Management Lead

QA Specialist

Clinical Director: MH, LD, Autism and Neurodivergence

Local Study Associate Director

Senior Clinical Pharmacist – 12 Month Fixed Term

Associate Director, Clinical Trial Disclosure & Transparency

Senior CRA

Senior/ Medical Writer - FSP

Manager II, Clinical Operations FSO and FSP (UK/IRE)

Health and Safety Advisor

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