Clinical Operations Manager

Clinical Lead

Permanent | Competitive salary

About Our Client

Our client is a well-established organisation operating in the clinical research and biotech space, partnering with sponsors on multi-regional studies. They are committed to gender equality and an inclusive work environment where everyone is treated fairly and with respect. Their culture supports flexibility, professional growth and a genuine focus on wellbeing, making it a strong setting for experienced clinical professionals who want to lead impactful work.

The Opportunity

This Clinical Lead position is a senior role with responsibility for providing direction and guidance to project teams across regions. You will coordinate site management and monitoring activities, and act as a key link between the project team and Project Manager, ensuring clinical operations run smoothly from start-up through to ongoing monitoring. It is an opportunity to use your expertise to influence study delivery while supporting and mentoring clinical teams.

Key Responsibilities

• Provide leadership, direction and guidance to the project team across multi-regional clinical studies.

• Coordinate site management and monitoring activities and communicate status updates to the Project Manager.

• Support and coordinate feasibility, site identification and site selection activities for multi-regional studies.

• Lead and assist with preparation of initial ethics and regulatory submission packages.

• Oversee approval processes and timelines to ensure studies progress as planned.

• Support the Project Manager with applications for Investigational Product (IP) and ancillary import/export permits and licences.

• Work with the Project Manager to coordinate initial IP shipment across regions.

• Lead internal CRA meetings and teleconferences, preparing sections of the agenda and following up on specific actions.

• Prepare agendas, meeting minutes and additional communication for internal meetings as required.

• Attend sponsor meetings and contribute to discussions, preparation of agendas and minutes as needed.

• Correspond directly with sponsors to provide information and updates where appropriate.

Minimum Qualifications & Experience

• Proven experience performing advanced clinical monitoring and site management tasks across multiple locations at a senior level.

• Demonstrated leadership skills with the ability to provide clear direction to clinical teams.

• Strong organisational skills and the ability to meet deadlines in a fast-paced, dynamic environment.

• Experience in coaching and mentoring clinical teams.

• Strong communication skills and fluency in verbal and written English.

Why Join Our Client’s Team?

• Work in an inclusive environment where diversity is welcomed and everyone is treated with respect.

• Access flexible working options to help balance professional and personal commitments.

• Benefit from paid parental leave for both parents and flexible leave entitlements.

• Take part in wellness initiatives that support your physical and mental wellbeing.

• Develop your career through ongoing development and training programmes.

• Contribute to meaningful clinical research and biotech projects with multi-regional impact.

How to Apply

If you meet the minimum qualifications and are ready to take on a senior leadership role in clinical research, we would like to hear from you. Please submit your application, outlining your relevant experience in advanced clinical monitoring, site management and team leadership.

Account Manager – Medical Communications – Hybrid

We are looking for an experienced Account Manager to take a central role in delivering high-quality healthcare communications across both medical affairs and publications. In this position, you will act as a trusted partner to clients, oversee projects from initial concept through to completion, and help shape the development of the wider team within a collaborative, hybrid working environment.

About Our Client

Our client is a dedicated healthcare communications agency working with organisations across the life sciences sector. They design and deliver strategic, evidence-led programmes that support better decision-making for healthcare professionals and improved outcomes for patients. You will be joining at a time of continued growth and demand for insightful, data-driven communication, with the opportunity to work on a diverse mix of projects. The team culture emphasises continuous learning, professional development, and working together to produce work that has a genuine impact.

The Role

As Account Manager, you will be responsible for managing day-to-day client relationships and ensuring that projects run smoothly across their full lifecycle. You will collaborate with senior colleagues to plan and deliver programmes, coordinate internal and external stakeholders, and provide clear, thoughtful guidance to clients. A key part of the role will be supporting and coaching junior team members, contributing to internal initiatives, and helping to strengthen the overall offering of the business.

Key Responsibilities

• Serve as the main point of contact for client accounts, building strong, long-term relationships and maintaining regular communication.

• Lead and coordinate projects across medical affairs and publications, from initial brief through planning, execution, and delivery.

• Work with senior colleagues to clarify objectives, shape strategy, and ensure projects are delivered to a high standard.

• Adapt your approach and communication style to suit different client expectations, therapeutic areas, and stakeholder groups.

• Facilitate effective information flow within the internal team to support smooth collaboration and timely delivery.

• Provide constructive feedback and day-to-day support to junior team members, helping them build skills and confidence.

Benefits

You will receive a competitive salary and a comprehensive benefits package designed to support your financial security, health, and work–life balance. This includes core benefits, flexible options, and access to wellbeing initiatives, alongside hybrid working and generous annual leave.

Why Apply?

This position is well suited to someone who enjoys owning client relationships, leading complex programmes in medical affairs and publications, and contributing to the growth of colleagues and the wider business. You will have the scope to influence project direction, the support of experienced senior team members, and the opportunity to develop your career within a flexible, supportive environment. If you’re ready to take the next step in healthcare communications, we encourage you to apply.

QC Chemist | Woking, Surrey | 12 Month FTC

Join a dynamic team as a QC Chemist/ Analyst at an esteemed international pharmaceutical company in this new contract role.

In this role, you'll gain training in a niche area of chemistry, contributing to a rapidly growing field. You'll have the opportunity to develop your skills and advance in your career while enjoying competitive remuneration. The ideal candidate will have worked in a pharmaceutical GMP laboratory previously – ideally with chromatography equipment.

This position involves shift work, so flexibility is key. The shift pattern rotates weekly as follows: 3am, 6am, 6am, 8am, 8am.

Key requirements:

• A degree in a Life Sciences discipline or equivalent

• Previous QC chemistry work experience in industry

• Familiarity with chromatography techniques such as HPLC and GC

• Understanding of GMP principles is preferred

• Flexibility to work shifts

If you're ready to join a supportive team and make your mark in the pharmaceutical industry, apply below for more information.

Keywords: QC, quality control, analyst, analytical, laboratory, GMP, entry level, graduate, science, pharmaceutical, biotechnology, manufacturing, shift work.

QC Chemist | Woking, Surrey | Permanent

Join a dynamic team as a QC Chemist/ Analyst at an esteemed international pharmaceutical company in this new permanent role.

In this role, you'll gain training in a niche area of chemistry, contributing to a rapidly growing field. You'll have the opportunity to develop your skills and advance in your career while enjoying competitive remuneration. The ideal candidate will have worked in a pharmaceutical GMP laboratory previously – ideally with chromatography equipment.

This position involves shift work, so flexibility is key. The shift pattern rotates weekly as follows: 3am, 6am, 6am, 8am, 8am.

Key requirements:

• A degree in a Life Sciences discipline or equivalent

• Previous QC chemistry work experience in industry

• Familiarity with chromatography techniques such as HPLC and GC

• Understanding of GMP principles is preferred

• Flexibility to work shifts

If you're ready to join a supportive team and make your mark in the pharmaceutical industry, apply below for more information.

Keywords: QC, quality control, analyst, analytical, laboratory, GMP, entry level, graduate, science, pharmaceutical, biotechnology, manufacturing, shift work.

🔬 QC Analyst | South London | Pharmaceutical Manufacturing

Looking for your next opportunity in Quality Control?

We're partnering with a pharmaceutical manufacturer seeking a QC Analyst to join a busy and growing Quality team. This is a fantastic opportunity for someone with analytical laboratory experience who enjoys working in a GMP-regulated environment and wants to contribute to product quality, compliance, and continuous improvement.

What you'll be doing:

✅ Testing raw materials, packaging components, in-process samples, and finished products
✅ Performing analytical testing using HPLC and GC techniques
✅ Supporting laboratory validation, calibration, and maintenance activities
✅ Conducting environmental monitoring and water sampling
✅ Investigating OOS results and supporting quality investigations
✅ Maintaining GMP-compliant documentation and data integrity standards
✅ Performing in-process quality inspections and production line checks
✅ Working closely with Quality, Production, and other cross-functional teams

What we're looking for:

✔ Degree in a Scientific discipline or equivalent
✔ Experience working within an analytical laboratory environment
✔ Strong understanding of GMP and Data Integrity requirements
✔ Hands-on experience with HPLC and GC, including troubleshooting instrumentation
✔ Excellent documentation and report-writing skills
✔ Strong attention to detail and a proactive approach to quality

This role would suit candidates from pharmaceutical, biotech, medical device, FMCG, food, or other regulated manufacturing environments who are looking to further develop their career within Quality Control.

📩 Interested in finding out more? Apply now or get in touch for a confidential discussion.

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QC Supervisor

Join a thriving team as a QC Supervisor at an esteemed international pharmaceutical company in this newly created permanent role.

This is an excellent opportunity for an experienced QC professional looking to take the next step into leadership. You'll be responsible for supervising a team of QC Chemists and Analysts, providing coaching and technical guidance, coordinating laboratory activities, and deputising for the QC Manager when required.

Working within a GMP-regulated laboratory, you'll play a key role in ensuring testing is completed to high quality standards while supporting the ongoing development of the team. The ideal candidate will have previous pharmaceutical QC experience and strong knowledge of analytical techniques such as HPLC and GC.

This position involves working 8 hour days from 6am or 8am – with flexibility required for the applicant to be available to work either shift,

Key Responsibilities

• Supervise and coordinate the daily activities of the QC laboratory team.

• Coach, mentor, and develop QC Chemists.

• Ensure testing is performed in compliance with GMP requirements and laboratory procedures.

• Support laboratory investigations, deviations, and OOS activities.

• Review data and documentation to ensure accuracy and compliance.

• Assist with workload planning and resource allocation.

• Deputise for the QC Manager when required.

• Drive continuous improvement initiatives within the laboratory.

Key Requirements

• Degree in Chemistry, Pharmaceutical Sciences, Life Sciences, or a related discipline.

• Circa 5 years+ experience working within a pharmaceutical GMP QC laboratory.

• Hands-on experience with analytical techniques such as HPLC and GC.

• Previous supervisory, mentoring, or team leadership is an advantage.

• Strong understanding of GMP and quality compliance requirements.

• Excellent communication and organisational skills.

If you're looking to progress your leadership career within a growing pharmaceutical business while remaining hands-on in a laboratory environment, apply below for more information.

Keywords: QC Supervisor, Quality Control Supervisor, Laboratory Supervisor, QC Team Leader, Analytical Chemist, HPLC, GC, GMP, Pharmaceutical, Biotechnology, Laboratory Management, Quality Control, Team Leadership, Pharmaceutical Manufacturing.