Account Manager, Medical Communications

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.

Clinical Operations Manager

Permanent

About Our Client

Our client is a well-established clinical research organisation operating in highly regulated environments, partnering with pharmaceutical and biotech companies to deliver complex clinical trials. They offer a collaborative, inclusive workplace where clinical operations professionals can contribute to meaningful research while benefiting from structured development, supportive leadership and modern flexible working practices.

The Opportunity

This Clinical Operations Manager position is ideal for an experienced clinical research professional who enjoys leading teams, shaping processes and influencing how trials are delivered. You will have genuine ownership over line management, operational oversight and resourcing, while working closely with project teams and senior management. The role offers a competitive salary together with strong benefits including flexible working options, wellness initiatives and ongoing development programmes.

Key Responsibilities

In this role, you will be responsible for ensuring that clinical trials are conducted in accordance with Good Clinical Practice (GCP), regulatory requirements, Standard Operating Procedures and project agreements, while leading and supporting members of our client’s team.

Line Management

• Act as line manager for one or more Clinical Leads and/or administrative staff within our client’s team.

• Work with Human Resources and senior management to identify resource needs and support hiring of new staff.

• Ensure all line reports receive appropriate induction and understand policies and procedures relevant to their role.

• Meet regularly with line reports to review and manage work quality, workload, welfare and development needs.

• Lead performance management activities including setting goals and objectives, competency assessments, salary reviews, promotions and succession planning.

• Review and assist with the development and maintenance of clinical operations processes, tools and SOPs.

• Review and approve internal expense requests in line with company policy.

• Review and approve leave requests in line with company policy.

Learning and Development

• Conduct accompanied monitoring assessments and co-monitoring visits to ensure compliance with SOPs, GCP and regulatory requirements.

• Contribute to the design and delivery of training to Clinical Operations staff, supporting skills growth across our client’s team.

Business Development and External Representation

• Represent our client at industry conferences and professional meetings as required.

• Support feasibility assessments and provide feasibility information to business development teams.

• Maintain a strong understanding of local and international clinical trial landscapes and provide informed advice to business development.

• Identify and highlight opportunities within projects or existing client relationships to expand business collaborations.

• Participate in bid defence and other business development meetings with local and international clients as a clinical operations representative.

• Establish and maintain relationships with key clinical trial sites and opinion leaders.

• Build and manage relationships with local third-party vendors such as central laboratories, depots, couriers, regulatory consultants and translation providers.

General Responsibilities

• Adhere to company policies, procedures and guidelines, maintaining a strong focus on quality in all activities.

• Identify areas of inefficiency in clinical operations and recommend improvements.

• Assist in the review and development of clinical operations SOPs and guidelines.

• Participate actively in the clinical operations group, including contributing to and presenting at clinical team meetings.

• Understand the responsibilities of our client as a service provider in the pharmaceutical industry.

• Ensure all communications with external parties and all aspects of study team performance present a positive professional image of our client.

About You

Our client is looking for a Clinical Operations Manager who brings both hands-on clinical research experience and proven leadership capability.

• Graduate in a life sciences related field and/or significant line management experience within the pharmaceutical industry.

• Experience in a Senior CRA, Project Manager or similar role, with considerable monitoring experience.

• Previous experience within a contract research organisation and line and/or matrix management experience are highly regarded.

• Able to balance operational oversight with people management, providing clear guidance while supporting autonomy and professional growth.

• Comfortable working in a fast-paced, regulated environment with multiple stakeholders and competing priorities.

How to Apply

If you are an experienced clinical research professional ready to take the next step into a broader leadership role, we would like to hear from you. Apply now to explore this opportunity to lead and shape clinical operations within a respected clinical research organisation.

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.