Director, Global Partnerhsip and Trial Optimization in Uxbridge

Director, Global Partnerhsip and Trial Optimization in Uxbridge

Uxbridge Full-Time 90000 - 110000 £ / year (est.) Home office (partial)
Initial Therapeutics, Inc.

At a Glance

  • Tasks: Lead strategic partnerships to enhance clinical trials and research initiatives.
  • Company: Join Regeneron, a pioneer in transforming lives through innovative medicines.
  • Benefits: Competitive salary, bonuses, health benefits, and comprehensive rewards package.
  • Other info: Inclusive workplace culture with opportunities for growth and development.
  • Why this job: Make a real impact in the life sciences industry while collaborating with top experts.
  • Qualifications: Experience in drug development and strong relationship management skills required.

The predicted salary is between 90000 - 110000 £ per year.

Build our future together

Regeneron is founded on the belief that the right idea, combined with the right team, can lead to significant transformations.

Our growing global network is dedicated to inventing, developing, and commercializing medicines that change lives for those with serious diseases.

In doing so, we are pioneering innovative approaches to science, manufacturing, and commercialization, as well as redefining our understanding of health.

We are seeking a Director, Global Development Strategic Partnerships to identify, establish, and manage strategic relationships with external organisations and institutions.

You will coordinate across a matrix of teams to create partnership opportunities that strengthen clinical development, clinical research, and Regenerons broader R&D objectives.

You will support partnership agreements from identification and evaluation through contract drafting, execution, and ongoing relationship management, working closely with internal leaders to maintain collaboration, continuity, and alignment.

When & where

Uxbridge (hybrid).

  • Discover your role
  • Develop a long-term, company-wide strategy for working with external organisations to support clinical trials and translational and basic research.
  • Identify and evaluate external partners based on agreed organisational needs, opportunities, and capability gaps.
  • Drive the evaluation and coordination of partnership opportunities, engaging internal experts when additional support is required.
  • Coordinate new opportunities with existing and prospective partner organisations.
  • Support contract drafting and execution while remaining connected to strategic relationships throughout the agreement lifecycle.
  • Manage and track external partnership opportunities in collaboration with project management and other external-facing colleagues.
  • Build consistent communication channels with internal and external partners to maintain continuity, alignment, and productive relationships.
  • You work collaboratively across functions to prioritise strategic partnerships and identify opportunities for innovation and efficiency.
  • This role requires
  • Previous experience and a deep understanding of the drug development process.
  • A proven track record of developing and maintaining partner relationships at all organisational levels.
  • Strong existing relationships and a positive reputation within the life sciences industry, particularly with academic medical centres and large health systems.
  • Strong business and financial management acumen, with experience in strategic planning and tactical execution.
  • The ability to manage and prioritise multiple tasks and projects with urgency while working within a matrix organisation.
  • Outstanding written, verbal, presentation, and consensus-building skills, with the ability to communicate accurately and concisely.

We are committed to building a workplace with an inclusive culture.

Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law.

Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.

Where necessary, we disclose salary ranges for roles in all countries in which we operate.

The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience.

In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits.

Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e. g. medical, dental, vision, life and disability), paid time off, and family support benefits.

For additional information about Regeneron benefits in the U.

S., please visit https://careers. regeneron. com/en/working-at-regeneron/total-rewards/.

For other locations, additional information will be provided during the recruitment process.

If you have any questions, please speak with your recruiter.

Please be advised that at Regeneron, we believe we do our best work when we are together.

For that reason, many roles are required to be performed onsite.

Please speak with your recruiter and hiring manager for more information about onsite expectations for your role and location.

As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based.

The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.

For jobs in Canada: this posting is for an existing position.

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Director, Global Partnerhsip and Trial Optimization in Uxbridge employer: Initial Therapeutics, Inc.

Initial Therapeutics, Inc. is an exceptional employer located in Harwell, offering a dynamic work environment that fosters collaboration and innovation in the field of immunoassays. With a strong commitment to employee growth, competitive benefits including healthcare and family support, and a culture that values diversity and equal opportunity, this role provides a meaningful opportunity for those looking to make a significant impact in clinical trials.

Initial Therapeutics, Inc.

Contact Details:

Initial Therapeutics, Inc. Recruitment Team

StudySmarter Expert Advice🤫

We think this is how you could land Director, Global Partnerhsip and Trial Optimization in Uxbridge

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We think you need these skills to ace Director, Global Partnerhsip and Trial Optimization in Uxbridge

Strategic Partnership Development
Clinical Trial Management
Drug Development Process Knowledge
Relationship Management
Business and Financial Acumen
Project Management
Contract Drafting and Execution

Some tips for your application 🫡

Showcase Your Relevant Experience:When applying for a role in the pharmaceutical industry, it's crucial to highlight any relevant experience you have. Whether that's internships, lab work, or even related coursework, make sure to weave this into your CV and cover letter. We want to see how your background aligns with the role you're applying for at Initial Therapeutics, Inc.!

Emphasise Your Understanding of Regulations:The pharmaceutical industry is heavily regulated, so it's important to indicate your familiarity with industry standards and regulations. In your cover letter, mention any training or certifications you've received that are relevant, or discuss projects where you’ve navigated compliance. This will show Initial Therapeutics, Inc. that you're not just a fit for the job but also a safety-conscious candidate!

Tailor Your CV to Be Result-Driven:Craft your CV to highlight quantifiable achievements, especially if you have previous roles in pharmaceuticals or related fields. Use metrics to demonstrate your impact, such as improved processing times or successful project completions while working on trials. This analytical approach will resonate well with hiring managers at Initial Therapeutics, Inc.!

Convey Your Passion for the Industry:In your cover letter, express why you are passionate about working in the pharmaceutical sector. Whether it’s your desire to contribute to groundbreaking drug research or improve patient outcomes, let it shine through! At Initial Therapeutics, Inc., we value candidates who are truly enthusiastic about their work—you might just stand out from the crowd.

How to prepare for a job interview at Initial Therapeutics, Inc.

Understand the Science

Make sure you brush up on key pharmaceutical concepts and recent developments in the industry. You might get asked some technical questions during the interview at Initial Therapeutics, Inc. that show your grasp of drug development processes or regulatory requirements, so be ready to discuss them clearly.

Showcase Relevant Experience

If you have any hands-on experience or internships in a laboratory setting, be sure to highlight these in your responses. Think about the projects you worked on, the methodologies you used, and the impact you made. It's all about telling a story that connects your background to the role you're applying for.

Know Their Products

Take some time to familiarise yourself with Initial Therapeutics, Inc.’s product range and recent breakthroughs. Understanding their portfolio not only shows your enthusiasm for the role but also allows you to ask insightful questions that demonstrate your interest in actively contributing to their projects.

Be Ready for Regulatory Scenarios

In a full-time pharmaceutical role, understanding the regulatory landscape is crucial. Prepare for situational questions that may test your problem-solving skills concerning compliance and safety standards. You could be asked how you'd handle a hypothetical issue regarding a drug’s market release, so think through your approach.