Manager, Trial Delivery Management in High Wycombe

Manager, Trial Delivery Management in High Wycombe

High Wycombe Full-Time 60000 - 80000 £ / year (est.) Home office (partial)
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At a Glance

  • Tasks: Lead and manage clinical trial activities, ensuring smooth execution and vendor oversight.
  • Company: Join a leading pharmaceutical company dedicated to innovative healthcare solutions.
  • Benefits: Competitive salary, health benefits, and opportunities for professional growth.
  • Other info: Dynamic work environment with travel opportunities across Europe and North America.
  • Why this job: Make a real impact in the healthcare industry while developing your leadership skills.
  • Qualifications: 8+ years in clinical research with strong leadership and project management skills.

The predicted salary is between 60000 - 80000 £ per year.

Responsible for the execution of study-level activities, creation and updating of trial-specific documents, vendor oversight & delivery, compound training, and other operational functions. The TDM coordinates country and regional operational delivery, aligning feasibility strategy, risk reviews, and local challenges that could impact overall study delivery.

Principal Responsibilities

  • Create and update critical trial-specific documents (e.g., Monitoring Guidelines, Informed Consent Form, Investigational Medicinal Product [IMP] related documentation).
  • Vendor set-up and day-to-day management of study vendors, including SOW creation and budget oversight.
  • Country/regional coordination of trial management activities and oversight (align feasibility strategy with local teams, perform country-level risk reviews, be aware of all projects across countries).
  • Support development of program-level compound training in collaboration with Clinical/CTL&D Medical writing.

Additional Responsibilities

  • Provide input into trial-level operational strategies.
  • Resolve trial-related issues and mitigate trial-related risks.
  • Participate in process improvement activities at a trial, compound & cross-DU level, as needed.
  • Provide support during Health Authority inspections and identify risks and mitigation plans at the program level for key issues.
  • Mentor & support onboarding of new team members, particularly those in Trial Management.
  • Foster employee engagement, inclusion, and Credo Behaviors.

Principal Relationships

  • Internal: Trial Management Directors, Clinical Trial Leaders, Clinical Trial Assistants, Delivery Operations representatives, other GD Functions and Clinical Teams, Procurement representatives.
  • External: Vendors.

Education and Experience Requirements

  • BS degree or equivalent (preferred Life Sciences such as Biology, Chemistry, Biochemistry, Nursing, Pharmacy).
  • Minimum of 8 years of related experience in pharmaceutical, biopharmaceutical, biotechnology, or healthcare industries.
  • Experience in and knowledge of the pharmaceutical development process, with clinical research operational knowledge across multiple phases (Phase I-IV).
  • 2-3 years’ experience leading multiple aspects of a global clinical trial.
  • Strong leadership, decision-making, analytical, financial management, and mentoring/coaching skills.
  • Excellent project planning/management, communication, and presentation skills.

Preferred Related Industry Experience

  • Pharmaceutical, biopharmaceutical, biotechnology.

Preferred Skills

  • Analytical reasoning, budgeting, clinical trial management systems (CTMS), compliance management, contract management, execution focus, fact-based decision making, laboratory operations, mentorship, process improvement, project integration management, research ethics, SOP creation, technical credibility.

Travel

Travel up to 15-20% of the time, defined by business needs.

Locations

  • High Wycombe, Buckinghamshire, United Kingdom
  • Beerse, Belgium
  • Milano, Italy
  • Madrid, Spain
  • Warsaw, Poland
  • Spring House, PA, United States
  • Toronto, Canada

Manager, Trial Delivery Management in High Wycombe employer: 6010-Biosense Webster Inc. Legal Entity

As a leading employer in the pharmaceutical industry, we offer a dynamic work environment in High Wycombe that fosters innovation and collaboration. Our commitment to employee growth is evident through comprehensive training programs and mentorship opportunities, ensuring that our team members thrive in their careers. With a strong focus on inclusion and engagement, we create a supportive culture where every voice is valued, making us an excellent choice for those seeking meaningful and rewarding employment.

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Contact Details:

6010-Biosense Webster Inc. Legal Entity Recruitment Team

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We think this is how you could land Manager, Trial Delivery Management in High Wycombe

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We think you need these skills to ace Manager, Trial Delivery Management in High Wycombe

Trial Management
Vendor Management
Budget Oversight
Feasibility Strategy
Risk Review
Clinical Research Knowledge
Leadership Skills

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 6010-Biosense Webster Inc. Legal Entity!

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 6010-Biosense Webster Inc. Legal Entity 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 6010-Biosense Webster Inc. Legal Entity!

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 6010-Biosense Webster Inc. Legal Entity, 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 6010-Biosense Webster Inc. Legal Entity

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 6010-Biosense Webster Inc. Legal Entity that show your grasp of drug development processes or regulatory requirements, so be ready to discuss them clearly.

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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.

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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.