Programme Executive (IME/CME)

Clinical Research Associate (Senior CRA / Principal CRA) – Remote, UK

Location: Fully remote with travel across England

Position type: Permanent

About Our Client

Our client is a well-established clinical research organisation operating within highly regulated environments, supporting complex, international clinical trials. Working across multiple therapeutic areas and trial phases, they focus on high-quality monitoring, balanced performance expectations and clear career pathways for their clinical operations professionals.

Our client’s team is known for promoting from within, supporting long-term careers in clinical research and offering flexible working arrangements that respect work-life balance. You will be joining a collaborative group of CRAs, study managers and operational specialists who share knowledge and support each other across remote locations.

The Opportunity

This is a permanent, fully remote Clinical Research Associate position, open at CRA II, Senior CRA or Principal CRA level depending on your experience and skill set. You will work across a variety of clinical trials and phases without being limited to specific therapeutic areas, giving you broad exposure and the chance to deepen your monitoring expertise.

The role offers a visible pathway for progression, with genuine potential to move quickly through levels based on performance and capability. You will benefit from balanced KPIs, realistic expectations around travel and a supportive structure that focuses on your development rather than simply maximising visit numbers.

Key Responsibilities

• Conduct independent on-site monitoring visits across England

• Perform all aspects of routine monitoring activities in line with protocols, SOPs and regulatory requirements across various trial phases.

• Build and maintain strong relationships with site staff to support study conduct, data quality and patient safety.

• Document monitoring activities comprehensively and ensure timely follow-up on action items.

• Collaborate closely with project teams, contributing to study management discussions and resolving site-related issues.

• Demonstrate flexibility around travel and site allocation, understanding that locations may vary according to business needs.

What Makes This Role Attractive

• Clear and visible career progression, with defined levels from CRA II through Senior CRA to Principal CRA, and examples of rapid promotion where merited.

• Balanced KPIs that allow you to focus on quality, development and long-term growth rather than only meeting high visit targets.

• Genuine work-life balance, supported by remote working and thoughtful study allocation.

• Near-site incentives and an approach to site allocation that aims to keep you predominantly within reasonable travelling distance, while recognising that some longer trips may be required.

• Access to peer and buddy programmes, offering mentoring, support and guidance from more experienced colleagues.

• Opportunities to progress into other suitable career pathways, depending on your interests and strengths.

Skills & Experience Required

• Strong, independent on-site monitoring experience in clinical trials,

• For Principal CRA / Lead CRA consideration, usually 6–8 years’ CRA experience, with a proven track record of handling complex studies and responsibilities.

• Experience across any therapeutic areas and clinical trial phases – there is no requirement for specific indication expertise.

• A valid driving licence and willingness to travel regularly for site visits.

• Life Sciences degree or relevant experience

• Right to work in the UK is essential; our client is unable to offer visa sponsorship.

Is This Role Right For You?

This position will suit you if you are an experienced CRA who values structured progression, realistic monitoring expectations and genuine work-life balance. If you enjoy independent on-site work, want to broaden your exposure across different studies and phases, and are looking for a remote role that still offers strong team connection and support, this could be an excellent next step.

How to Apply

If you meet the criteria outlined and would like to be considered for a CRA II, Senior CRA or Principal CRA level position, please submit your CV. We will review your experience, discuss your career ambitions and guide you through the next steps with our client.

Account Director – Medical Education (Remote, UK)

Are you an experienced Senior Account Manager or Account Director in Healthcare Communications, equipped with a Medical Education (IME or CME) background? If you're ready to make a meaningful difference while working in a fast-paced, rewarding environment, our client wants to hear from you.

About Our Client

Our client is a forward-thinking organisation specialising in Medical Education, committed to improving access to crucial medical education globally. By leveraging innovative approaches, they work to bridge healthcare knowledge gaps and improve outcomes through enduring and live formats.

Why Join Our Client’s Team?

• Thrive in a high-velocity environment where urgency meets excellence in delivery.

• Take charge of programme execution, combining precision, creativity, and impact.

• Become a part of a collaborative team dedicated to improving global healthcare education.

• Benefit from the flexibility of fully remote working while contributing to impactful projects.

Your Role as an Account Director

In this crucial position, you’ll lead the delivery of multiple educational initiatives, overseeing both live and on-demand formats. As a key operational link across various teams, you’ll be pivotal in ensuring high-quality, timely, and accurate execution of programmes that truly make a difference.

Key Responsibilities

• Take end-to-end ownership of programme delivery, from internal kick-off to final execution, for live and enduring educational activities.

• Plan, support, and manage live events such as webinars or virtual symposia, handling everything from platform setup to rehearsal logistics.

• Act as a primary point of contact for faculty members, ensuring they are supported, informed, and consistently deliver at a professional standard.

• Collaborate with cross-functional teams to maintain alignment and operational efficiency across projects.

What We’re Looking For

The ideal candidate will bring:

• Previous experience delivering Medical Education programmes (IME or CME) within an medcial communications agency

• Exceptional organisational skills and the ability to manage multiple concurrent projects seamlessly.

• A strong eye for detail combined with a commitment to excellence in programme delivery.

• Outstanding stakeholder management and communication abilities.

What’s on Offer?

• The chance to work remotely within the UK while being part of transformative healthcare projects.

• A collaborative and professional work environment focused on impactful outcomes.

• Opportunities to innovate, contribute, and grow in a company genuinely driven by a mission to improve healthcare education.

Location

This is a remote position, open to candidates based in the United Kingdom.

Ready to Take the Next Step?

If you're a driven professional with a passion for healthcare communications and the skills to lead, apply today to join our client’s inspiring team. A rewarding career focused on meaningful work awaits!

Associate Director Cyber Security | Permanent Role

$160,000 - $200,000 base

Location: Gaithersburg, MD or Radnor, PA - Onsite 5 days a week

Our client, a leader in their field, is seeking a talented and experienced Associate Director of Cyber Security to join their close-knit team. This permanent role offers a unique opportunity to take the lead in shaping the security strategy while contributing to the protection of a dynamic and progressive enterprise. If you're ready to bring your expertise to a key leadership position, this role is for you.

About the Role

As the Associate Director of Cyber Security, you will take charge of ensuring the safety, compliance, and reliability of our client’s systems and data infrastructure. This is a challenging role that requires both strategic vision and hands-on leadership to maintain a robust security posture across multi-cloud and on-premises environments. You’ll work directly with external SOC teams, senior stakeholders, and internal teams to manage, assess, and mitigate cyber risks.

Key Responsibilities

• Lead and develop security operations, including strategy and incident response frameworks.

• Own and operate critical platforms such as SIEM, SOAR, EDR, and vulnerability management systems.

• Develop and manage security policies, roadmaps, and risk registers in compliance with frameworks such as ISO 27001, NIST, and GDPR.

• Manage relationships with external SOC providers, ensuring SLAs and escalation procedures are met.

• Provide mentorship and strategic leadership to security staff, fostering development and skill growth.

• Implement and audit controls against CIS benchmarks for Linux and Windows-based systems.

• Communicate complex security risks effectively to senior stakeholders and non-technical audiences.

Essential Qualifications

• Bachelor's degree in Cyber Security, Information Security, Computer Science, or a related field.

• A minimum of 4 years in a senior cyber security role (L3 or higher).

• Industry-recognized certifications such as CISSP, CISM, CISA, or CCNP Security.

• Strong experience with security frameworks and regulatory standards (ISO 27001, NIST, GDPR).

• Proven expertise in multi-cloud environments (Azure/AWS) and hybrid on-premises systems.

• Deep knowledge of security hardening principles and auditing practices.

• Exceptional leadership and stakeholder engagement skills.

Why Join Our Client?

Our client prides themselves on fostering an inclusive and professional culture where every team member is empowered to make real contributions. In this collaborative environment, you’ll have the opportunity to influence meaningful and cutting-edge cybersecurity initiatives while developing your career as a valued leader in the field. You’ll work alongside professionals who are committed to excellence and innovation.

Interested?

If you are ready to take the next step in your career and bring your cyber security expertise to a leadership role, our client would love to hear from you. Apply today and help drive the future of cyber resilience!

Interim Head of QC

3-6 months - strong likelihood of extension.

IR35: Inside

About the Role

In this role, you’ll have the opportunity to lead and oversee Quality Control processes, ensuring that all manufacturing outputs meet the highest quality standards. Process improvement and implementing a continuous improvement mindset is critical. This role is not just about identifying the improvements - it needs to make them happen.

Key responsibilities include:

• Directing all Quality Control activities to ensure compliance with internal and external standards.

• Leading and mentoring our client’s QC team, driving a culture of quality and continuous improvement.

• Collaborating with cross-functional stakeholders to address quality-related challenges and develop sustainable solutions.

• Acting as a key decision-maker in Quality Assurance and Quality Control processes to support manufacturing excellence.

What We’re Looking For

• Previous senior QC leadership experience (QC Chemistry) within a pharmaceutical GMP environment 

• Previous leadership of QC teams essential

• Track record of coaching and mentoring 

• Experience in continuous improvement across QC processes

• Experience of a CDMO / client led / fast paced environment is a strong advantage

QC, quality, control, analytical, chemistry, leadership, manager, head, supervisor, leader, HPLC, GC, chromatography, QA, continuous, improvement.

Study Monitoring Lead
Department: Global Clinical Operations

Position Summary
The Study Monitoring Lead is responsible for the operational oversight of global clinical trials, ensuring studies are executed in accordance with protocol, timelines, ICH-GCP, regulatory requirements, and company SOPs. The SML oversees study feasibility, site management, monitoring activities, and CRO/vendor performance while partnering with cross-functional teams to drive successful study execution.

Responsibilities

• Lead study feasibility activities, evaluating country and site capabilities, patient access, and operational readiness.

• Partner with the Clinical Study Manager, Clinical Study Physician, and CROs to support country and site selection.

• Oversee site activation activities, including regulatory documentation, contracts, investigational product supply, laboratory kits, and other start-up requirements.

• Monitor site activation, enrollment, protocol compliance, and data quality.

• Prepare, review, or approve Monitoring Plans, Laboratory Manuals, patient-facing materials, and other operational study documents.

• Oversee CRO and vendor performance related to site management and monitoring.

• Support training for CRO Clinical Trial Leads, CRAs, and investigative sites.

• Oversee remote and on-site monitoring activities, ensuring timely visit completion, issue resolution, and follow-up.

• Conduct sponsor co-monitoring visits and perform monitoring or co-monitoring activities as needed.

• Track study metrics, including site activation, enrollment, monitoring visits, protocol deviations, and overall study progress.

• Oversee biological sample tracking and investigational product management with study stakeholders.

• Collaborate with Clinical Operations, Data Management, Medical, Safety, Regulatory, Clinical Supply, CROs, vendors, investigators, and study sites to ensure efficient study execution.

• Identify and resolve operational risks, escalating issues when appropriate.

• Ensure compliance with study protocols, ICH-GCP, regulatory requirements, and company SOPs while supporting inspection readiness.

Qualifications

• Master's degree in Life Sciences or a related field.

• 5+ years of clinical operations experience, including 3+ years monitoring oncology studies as a CRA or comparable site management role.

• Experience with study feasibility, site selection, site activation, monitoring oversight, and CRO/vendor management.

• Strong knowledge of ICH-GCP, global clinical trial regulations, and inspection readiness.

• Excellent communication, collaboration, organizational, analytical, and problem-solving skills.

• Ability to travel internationally as required.

Analytical/QC Project Chemist

Location: South Yorkshire, West Midlands or North-West - with flexibility to travel

We’re supporting the growth of a new specialist QC function within a dynamic, multi-site pharmaceutical operation across the UK. This is a project-focused role working alongside a dedicated validation team, supporting new product introductions, method development, and technical transfer across multiple UK sites.

You’ll play a key role in bringing new methods into GMP QC environments, scaling processes, and embedding robust validation practices across the network.

What you need to know

• Multi-site role – based out of a North UK facility but with travel required across all UK sites

• Working closely with a central validation team, while remaining part of the wider QC function

• Reporting line into QC leadership, with strong project-based collaboration

• Focus on new product introduction, validation and tech transfer before handover to local QC teams

• Core responsibilities include: 

  • Method validation and transfer (some method development)

  • Scaling up analytical methods for routine QC use

  • Training QC teams on validated methods

What you need to bring

• 2–3 years’ experience in a GMP QC or analytical environment

• Demonstrated expertise in analytical method validation – not just some exposure, but independent troubleshooting and problem solving

• Hands-on experience with HPLC and GC techniques

• Strong understanding of GMP requirements within a regulated setting

• Experience supporting method development, optimisation, or tech transfer

• Ability to work in a project-driven, multi-site environment

• Confident communicator, capable of training and supporting QC teams during method handover

QC, control, quality, analytical, chemist, method, validation, HPLC, chromatography, GC, transfer, scale, tech, manufacturing, development, validate, wet, TLC, bench