Associate Director - Healthcare Communications

Senior Medical Writer – Join Our Client's Collaborative Team

Are you a seasoned Medical Writer with a passion for contributing to impactful clinical and regulatory projects? Our client is seeking a highly skilled and motivated Senior Medical Writer to be an essential part of their dynamic team. This is a permanent, full-time role suited for professionals with over 5 years of experience who thrive in an innovative and collaborative environment.

About the Role

As a Senior Medical Writer, you will play a client-facing role, working closely with medical monitors and senior leadership to develop high-quality medical and regulatory documentation. Your expertise and collaborative nature will help shape scientific narratives across multiple projects. This position gives you the opportunity to contribute to critical regulatory submissions, support strategic discussions, and make a meaningful impact within a supportive and professional organisation.

Key Responsibilities

• Prepare a range of regulatory documents, including Investigational New Drug (IND) applications, clinical study protocols, Investigator Brochures, and Clinical Study Reports.

• Develop and update critical documents such as IND Annual Reports, Development Safety Update Reports (DSURs), and Patient Informed Consent Forms.

• Collaborate across functions to provide guidance and support in the preparation and review of training guidelines, manuals, and similar documentation.

• Offer mentoring to new medical writers by providing constructive feedback, direction, and support.

• Engage directly with clients and cross-functional experts, managing timelines, coordinating reviews, and overseeing review meetings with professionalism and confidence.

What You Need

• Bachelor’s degree is required, and an advanced degree is preferred.

• At least 5 years of experience in a CRO or pharmaceutical environment, with at least 3 years in regulatory medical writing focusing on oncology.

• Proven ability as a lead writer for multiple document types, including Clinical Study Protocols, Investigator’s Brochures, DSURs, and IND applications.

• Experience collaborating with clients or sponsors, managing timelines, organising review cycles, and coordinating review meetings.

• Familiarity with electronic Common Technical Document (eCTD) modules and fast-track application processes such as INDs and BTDRs.

• Strong understanding of industry principles related to drug safety, regulatory guidelines, clinical trials, oncology, and pharmacology.

• Exceptional organisational skills with the ability to manage multiple priorities and projects simultaneously.

• Outstanding communication and interpersonal skills, alongside advanced proficiency in MS Office software.

What’s on Offer

Our client offers the opportunity to work remotely across the UK providing you with flexibility whilst being part of a collaborative and innovative team. This role combines professional development, visibility in critical projects, and the chance to directly impact meaningful clinical and regulatory initiatives.

About Our Client

Our client is a well-respected and innovative organisation dedicated to delivering high-quality medical and regulatory solutions. Their team operates in a supportive and professional environment that values collaboration and excellence. With extensive expertise and a client-focused approach, our client is at the forefront of clinical and regulatory writing, offering team members the opportunity to advance their skills and contribute meaningfully to projects that matter.

Apply Today

If you are ready to take the next step in your career as a Senior Medical Writer and join a forward-thinking organisation, we’d love to hear from you. Apply now and become part of an inspiring team that thrives on excellence and collaboration.

Territory Sales Manager - UK based (must be in/close to Oxford/Cambridge/London)

Role Overview

Are you ready to take the reins as a Territory Sales Manager, influencing key stakeholders and driving success in the Golden Triangle, UK? This exciting role offers the chance to collaborate with industry leaders, representing innovative solutions in Instrumentation & Laboratory Automation. If you’re passionate about building client relationships and delivering measurable growth, this is the opportunity you’ve been waiting for.

About Our Client

Our client is a forward-thinking organisation operating at the cutting edge of Laboratory Automation & Sample Management. With a focus on innovation and customer satisfaction, they empower their team to contribute meaningfully while working in a supportive and flexible environment.

About the Role

• Develop and manage strong client relationships to drive the adoption of advanced instrumentation solutions in laboratories.

• Identify key opportunities across the territory and implement tailored strategies to achieve measurable growth and market expansion.

• Collaborate with internal teams to provide client-focused services, ensuring satisfaction and long-term partnerships.

• Act as a trusted advisor to clients, demonstrating expertise in laboratory workflows and automation products.

Skills

• Experience in sales related to Life Science Instrumentation/Lab Automation/Sample Management, with a proven ability to engage and influence decision makers.

• Strong self-motivation for working autonomously in a remote capacity while meeting ambitious targets.

• Proven interpersonal skills to manage diverse stakeholders effectively within the scientific and laboratory sectors.

Next Steps

Ready to make a move? Submit your application today to explore this brilliant opportunity.

Role Overview

Are you a seasoned Cost Engineer ready to make an impact in the world of large-scale capital projects? Join our client’s team on a two-year contract and play a pivotal role in driving the financial success of their Global Engineering initiatives. With a focus on planning, execution, and financial control, this position is a unique opportunity to collaborate across dynamic teams and add value to highly regulated industries. This office-based role offers the chance to bring your analytical expertise to life in managing complex, high-stakes projects.

About Our Client

Our client is a global leader in operations and manufacturing, dedicated to engineering excellence and innovation within highly regulated environments. With a strong commitment to collaboration and best practices, they provide a platform where experienced professionals can contribute to challenging and impactful projects, all while developing their expertise in capital engineering solutions.

About the Role

• Develop and manage project cost estimates throughout all phases, from concept to closeout.

• Establish budgets, cost baselines, and accurate cash flow forecasts for multi-faceted projects.

• Monitor expenditures, analyze financial risks, and proactively address trends and variances.

• Collaborate with project managers, engineering, procurement, and finance teams to ensure seamless cost tracking and reporting.

• Prepare executive-level cost reports and dashboards to guide critical decision-making.

• Ensure compliance with industry standards, company policies, and financial controls.

• Drive continuous improvement through cost control procedures and benchmarking analysis.

Requirements / Experience

• Minimum 5+ years of cost engineering or project controls experience.

• Expertise in capital projects within regulated industries such as pharmaceutical or biotechnology.

• Proficiency in cost management tools like SAP, Primavera P6, EcoSys, or similar platforms.

• Advanced Microsoft Excel skills, including data analysis and reporting.

Skills

• Strong analytical abilities for accurate budgeting and forecasting.

• Collaborative approach to cross-functional teamwork.

• Effective communication skills to present financial data to key stakeholders.

• Technical proficiency in cost management systems to enhance project outcomes.

Next Steps

Ready to advance your career with a pivotal role in capital project engineering? Apply now and take the first step in joining our client’s exceptional team. We look forward to hearing from you!