Clinical Development Associate

Clinical Development Associate

Location: Cambridge, Hybrid

Department: Clinical Development

Job type: 1 Year Fixed-Term Contract

Join us and make a difference when it matters most 

At Mundipharma, we are proud of the work we do to bring innovative treatments to patients. We challenge ourselves constantly to deliver more for patients, healthcare professionals, our partners, and our employees. 

The Team

The Clinical Development Associate will join the Clinical Development team in Cambridge on a 1-year fixed-term contract. This role is ideal for a recent postgraduate or early-career professional with a strong interest in clinical research, data analysis, and medical writing. The successful candidate will play a key role in supporting clinical development activities, with a particular focus on data-driven insights, operational coordination, and scientific documentation.

Role and Responsibilities

• Analyse published clinical and medical data across the company's portfolio, supported by advanced AI tools.

• Assist in the preparation of documents for regulatory submissions, and internal presentation.

• Support content creation for clinical documents including investigator brochures, clinical study reports, and regulatory correspondence.

• Ensure scientific accuracy and compliance with applicable guidelines and standards.

• Maintain accurate records and contribute to the development of standard operating procedures and templates.

• Support the team in preparing for audits and inspections.

• Co-ordinate activities relating to HCP and vendor engagement.

What you'll bring

• Bachelor or Masters degree or equivalent in life sciences, pharmacy, medicine, or a related field.

• Strong analytical skills and familiarity with Microsoft365.

• Previous Veeva CRM experience would be advantageous but not essential

• Excellent written and verbal communication skills.

• Clear scientific writing and slide‑building skills; ability to synthesize complex data for non‑statistical audiences.

• Prior experience in clinical research or medical writing is desirable but not required.

• Ability to work independently and collaboratively in a fast-paced environment.

What we offer in return

• Opportunity to contribute to impactful clinical research projects.

• Exposure to cross-functional teams and global clinical development processes.

• Mentorship and training in clinical operations, data analysis, and medical writing.

• Flexible benefits package

• Opportunities for learning & development through our varied programme 

• Collaborative, inclusive work environment

Diversity and inclusion

Building an inclusive environment where people can thrive, grow and achieve their full potential is a priority. We believe this isn't just the right thing, but also the smart thing to do. We are on a journey and will seek to move forward together through education and awareness to build a culture that welcomes and celebrates diversity and uniqueness. We will create a workplace environment where everyone can, every day, bring their authentic selves and is treated with dignity and respect. 

About Mundipharma

Mundipharma is a global healthcare company focussing on customers across Africa, Asia Pacific, Canada, Europe, Latin America, and the Middle East.  

Mundipharma is dedicated to bringing innovative treatments to patients in the areas of pain management, infectious disease as well as other severe and debilitating disease areas. Their guiding principles, centered around Integrity and Patient-Centricity, are at the heart of everything they do. For more information visit   

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