Clinical research Work, Jobs in Sherborne St. John, Ham (with Salaries)

Clinical Research Scientist
Montu UK —Winnersh
- £60,000 - £65,000 a year
- Full-time
- Hybrid work
- Analysis skills
- Project management
- Organisational skills
6d
Senior Clinical Project Support Specialist - Sponsor dedicated (m/w/d)
IQVIA —Reading
- From £58,500 a year
- English
- Microsoft Office
- Bachelor's degree
Study Start Up Associate
ICON Plc —Reading
- Full-time
- Bachelor's degree
- Travel
- Organisational skills
- Employee assistance programme
4d
Sr. CRA 1 - Site Management
IQVIA —Reading
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Clinical Trial Associate
ICON Plc —Reading
- Full-time
- Bachelor's degree
- Travel
- Organisational skills
- Employee assistance programme
7d
Clinical Trial Program Lead
Eli Lilly —Bracknell
- Full-time
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
CRA 2 - Single Sponsor Dedicated
IQVIA —Reading
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
CRA
ICON Plc —Reading
- Full-time
- Travel
- Communication skills
- Nursing
- Employee assistance programme
11d
Sr. Clinical Project Manager (Europe)
Allucent —Bracknell
- Hybrid work
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
- Flexible schedule
- Referral programme
Quick apply
Head of Patient Science, Instrument Development & Thought Leadership
IQVIA —Reading
- Doctoral degree
- Master's degree
- Leadership
12d
Senior Study Start Up Associate
ICON Plc —Reading
- Full-time
- English
- Bachelor's degree
- Travel
- Employee assistance programme
6d
Senior Clinical Programmer I
Allucent —Bracknell
- Full-time
- Hybrid work
- Computer Science
- Bachelor's degree
- Flexible schedule
- Referral programme
Quick apply
Sr. CRA 1 - Single Sponsor Dedicated
IQVIA —Reading
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Senior CRA
ICON Plc —Reading
- Full-time
- Patient monitoring
- Bachelor's degree
- Travel
- Employee assistance programme
7d
Clinical Trial Manager - Project Lead
ICON Plc —Reading
- Full-time
- Oracle
- Management
- Project management
- Employee assistance programme
3d
Assoc Director, Quality Management - Client Dedicated Clinical Compliance Optimization Lead
IQVIA —Reading
- English
- Microsoft Office
- Bachelor's degree
3d
Project Manager I, IDEA
ICON Plc —Reading
- Full-time
- Project management
- Bachelor's degree
- Communication skills
- Employee assistance programme
5d
Director, Remote Research Clinicians
IQVIA —Reading
- Remote
- Bachelor's degree
- Communication skills
5d
Clinical Supplies Project Manager
ICON Plc —Reading
- Full-time
- Management
- Project management
- Bachelor's degree
- Employee assistance programme
23h
Local Study Associate Director
IQVIA —Reading
- Patient monitoring
- English
- Project management
5d

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clinical research jobs near sherborne st. john, ham

Clinical Research Scientist

Montu UK -
Winnersh

Apply Now

Job details

Full-time
£60,000 - £65,000 a year
6 days ago

Benefits

Company pension
Private medical insurance
Enhanced maternity leave
Enhanced paternity leave

Qualifications

Statistical software
Clinical research
Pain management
Analysis skills
Project management
Organisational skills
Leadership
Communication skills

Full job description

About the role
We are recruiting a Clinical Research Scientist to join our team. This is a fantastic opportunity for an experienced clinical research professional to lead the delivery of high-quality research projects that generate meaningful evidence and improve patient outcomes.

As a Clinical Research Scientist you will oversee the day-to-day management of multiple research studies, ensuring projects are delivered to the highest scientific, ethical, and regulatory standards. You will play a key role in embedding research into clinical practice while working collaboratively with clinicians, governance teams, data specialists, and external partners.

This is a hands-on leadership role where you will combine project management, research expertise, and people leadership to ensure studies are delivered efficiently while maintaining a strong focus on quality, compliance, and continuous improvement.

Key responsibilities

As a Clinical Research Scientist, you will:

Lead the delivery of clinical and real-world evidence research projects from set-up through to completion.
Develop research protocols, study documentation, ethics applications, governance submissions, SOPs, and operational processes.
Manage and mentor research staff, supporting their development while maintaining high standards of scientific and operational excellence.
Oversee participant recruitment, follow-up, data collection, quality assurance, and study compliance.
Monitor study progress, identify risks, and implement solutions to ensure successful project delivery.
Ensure all research activities comply with Good Clinical Practice (GCP), GDPR, research governance, and regulatory requirements.
Analyse and interpret research data to support evidence generation and improve patient outcomes.
Prepare research reports, publications, presentations, and evidence summaries.
Work collaboratively with multidisciplinary teams, academic partners, and external stakeholders to integrate research into clinical care.
Build strong relationships across internal and external teams to support successful research delivery.

What we are looking for

Degree in Life Sciences, Clinical Research, Public Health, Medicine, Pharmacy, Nursing, or a related discipline.
Significant experience delivering clinical research within healthcare, academia, life sciences, or another regulated environment.
Experience leading research projects and managing research teams.
Strong knowledge of Good Clinical Practice (GCP), research governance, ethics, informed consent, GDPR, and UK clinical research regulations.
Understanding of UK healthcare systems, including NICE guidance and NHS structures.
Strong project management and organisational skills with the ability to manage multiple priorities.
Excellent analytical skills with experience interpreting healthcare or clinical research data.
Confident communicator with excellent written and verbal communication skills.
Proven ability to work effectively with multidisciplinary teams and external research partners.
Experience within medical cannabis, chronic disease, pain management, health economics, outcomes research, or statistical software would be advantageous but is not essential.
Highly organised, detail-oriented, and able to manage complex research programmes in a fast-paced environment.

What we offer

Benefits include:

25 days holiday, rising to 27 after year one and 30 after year three, plus 8 bank holidays
Pension matching up to 5% employer contributions
Private healthcare scheme
Enhanced maternity and paternity leave
Cycle-to-work and EV scheme
Genuine growth: collaboration across teams, representation at industry events, and direct involvement in shaping a scaling business

About Montu

Montu UK is the leading digital health company specialising in cannabis-based medicines, dedicated to improving patient access to safe and effective treatments. Our mission is to transform lives by combining innovative technology with high-quality clinical care, ensuring patients receive the support they need at every step of their journey.

As a fast-growing organisation, we offer a collaborative environment where talented people develop their careers whilst contributing to meaningful change in healthcare. Your work here has a direct impact on patients' lives and on expanding access to modern medical treatments.

Compensation Range: £60K - £65K

Apply Now

Refine Your Search

clinical research jobs in sherborne st. john, ham

Clinical Research Scientist

Senior Clinical Project Support Specialist - Sponsor dedicated (m/w/d)

Study Start Up Associate

Sr. CRA 1 - Site Management

Clinical Trial Associate

Clinical Trial Program Lead

CRA 2 - Single Sponsor Dedicated

CRA

Sr. Clinical Project Manager (Europe)

Head of Patient Science, Instrument Development & Thought Leadership

Senior Study Start Up Associate

Senior Clinical Programmer I

Sr. CRA 1 - Single Sponsor Dedicated

Senior CRA

Clinical Trial Manager - Project Lead

Assoc Director, Quality Management - Client Dedicated Clinical Compliance Optimization Lead

Project Manager I, IDEA

Director, Remote Research Clinicians

Clinical Supplies Project Manager

Local Study Associate Director

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