JOB DESCRIPTION – Development Project Manager

THE COMPANY

Glen Clova Scientific Ltd (GCS) is developing a new generation of Active Biologic drugs to treat inflammatory conditions. We are an ambitious spinout from the University of Dundee aiming to address a global need to make effective treatments available for millions of patients in our clinical areas. Our novel Virus-Like-Particle technology is poised to address inherent limitations of the current blockbuster class of biologic drugs. Our vision is to make innovative therapeutics more accessible to patients than current blockbusters and improve quality of life in poorly served patient populations. If you aspire not only to be at the core of biotech innovation but also to tackle the global problem of high-cost medicines, this is a rare opportunity to join a highly dynamic team.

The company is headquartered in Scotland with an R&D facility near Dundee. This position may be a remote role but will require regular travel to Dundee and regular travel to international development partners.

JOB DESCRIPTION

We are seeking an experienced and drivenDevelopment Project Manager within therapeutic drug/vaccine development to coordinate our preclinical programs. This role is critical to ensuring the successful execution of our R&D pipeline; working cross-functionally with internal teams and external partners to deliver high-quality data packages on time and within budget to support project progression to clinical development.

KEY ACTIVITIES

• Support the planning, execution, and tracking of preclinical development projects from early discovery through IND-enabling studies and regulatory submission
• Oversee submissions to scientific advice committees and involvement in novel vaccine applications to regulatory bodies, such as the EMA/MHRA
• Develop and maintain detailed project plans, timelines, budgets, and risk registers.
• Contribute to the preparation of key documentation, including regulatory documentation, grant applications
• Track and communicate project performance, status, and key decisions to stakeholders and leadership
• Coordinate cross-functional teams including biology, pharmacology, toxicology, CMC, and regulatory affairs
• Manage relationships with CROs and academic collaborators to ensure timely and quality delivery of outsourced studies
• Ensure compliance with regulatory and quality standards throughout project execution.

Experience and Qualifications

EXPERIENCE AND QUALIFICATIONS

• 5+ years’ experience in pharma/biotech industry with a strong focus on therapeutic drug development
• 3+ years’ project management experience in pharmaceutical or biotech setting
• BSc/MSc in a related scientific field, e.g. immunology, autoimmunity. PhD desirable
• Proven track record of managing complex R&D projects and cross-functional teams
• Expertise with project management software
• Familiarity with creation, implementation, communication and reporting of project budgets
• Excellent organisational and verbal and written communication skills
• Excellent interpersonal and problem-solving skills
• Strong ability to manage multiple and varied tasks
• Demonstrate initiative and ability to work independently
• PMP or equivalent project management certification would be desirable
• Ability to work remotely if required

ADDITIONAL BENEFITS

• Employer contributions into a personal private pension plan as % of income
• Employee stock option plan after qualifying period
• Life insurance & optional health insurance after qualifying period

WHAT WE OFFER

The opportunity to be part of a mission-driven company at the forefront of biologics innovation.

• A collaborative and inclusive work environment
• Competitive salary and benefits package
• Flexible working arrangements and professional development support

Pay: £50-60k per year depending on experience

Job Type: Full-time

Working days: Monday to Friday

Please apply with your CV to info@glenclovascientific.com

Please note that only qualified candidates will be contacted for further consideration.