Sr. CTM Associate in Uxbridge

Sr. CTM Associate in Uxbridge

Uxbridge Full-Time 36000 - 60000 £ / year (est.) No home office possible
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At a Glance

  • Tasks: Support global clinical trials and ensure compliance with protocols and regulations.
  • Company: Join Kite, a Gilead Company, leading in cancer immunotherapy innovation.
  • Benefits: Competitive salary, health benefits, and opportunities for professional growth.
  • Why this job: Make a real difference in cancer treatment while working with cutting-edge therapies.
  • Qualifications: Degree in a scientific discipline and experience in clinical trials, especially oncology.
  • Other info: Collaborative environment with a focus on integrity, teamwork, and inclusion.

The predicted salary is between 36000 - 60000 £ per year.

Kite, a Gilead Company, is a biopharmaceutical company that is engaged in the development of innovative cancer immunotherapies. The company is focused on chimeric antigen receptor and T cell receptor engineered cell therapies. The Clinical Operations team is responsible for the execution of all Phase 1-4 clinical trials, across all therapeutic areas, around the world. In partnership with Clinical Research, Medical Affairs and other Development Operations functions, Clinical Operations ensures that all clinical trial activities are performed in accordance with applicable SOPs, company policies and regulatory guidelines to provide timely delivery of high quality clinical data to support global registration and commercialization of Kite/Gilead’s products.

Essential Duties and Job Functions

  • Assist global and regional trial managers with set‑up of central labs and study vendors as required, including liaising with study management CRO to ensure site training and timely initiation.
  • Perform accompanying visits (PSSVs, SIVs, RMVs) with CRO CRAs to ensure correct study procedures according to Gilead SOPs and protocol procedures, and review of routine regulatory documents/files in compliance with protocol, regulatory requirements, SOPs, and Monitoring Plan, as required.
  • Under supervision may assist in review of protocols, informed consents, and case report forms, monitoring plans, abstracts, presentations, manuscripts and clinical study reports.
  • May assist in compilation of investigator brochures under close supervision.
  • Review of trip reports generated by CRO CRAs.
  • Communicate and collaborate with other functional groups including but not limited to Clinical Research, Regulatory Affairs, CCF, Materials and Logistics (M L), and Drug Safety and Public Health (DSPH) to ensure efficient management of study activities.
  • Assist in the Management of the CRO’s and vendor’s as required.
  • Assist with the preparation and organization of international investigator meetings.
  • Assist in preparation of safety, interim and final study reports, including resolving data discrepancies.
  • Perform administrative duties in a timely manner as assigned.
  • Travel may be required 1 or 2 times per year (a few days).

Experience, Knowledge and Skills

  • Educated to degree level or equivalent in a scientific discipline.
  • Previous experience of pharmaceutical clinical trial experience.
  • CRA experience is highly desired.
  • Oncology experience is required / CAR‑T Cell Therapy would be desirable.
  • Excellent verbal, written, interpersonal and presentation skills are required.
  • Must be familiar with routine medical/scientific terminology.
  • Must be proficient with Word, PowerPoint, and Excel.
  • Knowledge of FDA and/or EMEA Regulations, ICH Guidelines, and GCPs governing the conduct of clinical trials is desirable.
  • The candidate should be skilled in communication, time management, organization, and prioritization.
  • Previous experience in clinical research sites/hospitals, CROs, or pharmaceutical companies is desirable.
  • Knowledge of European regulations for clinical trials is desirable.

Gilead Core Values

  • Integrity (always doing the right thing)
  • Teamwork (collaborating in good faith)
  • Excellence (working at a high level of commitment and capability)
  • Accountability (taking personal responsibility)
  • Inclusion (encouraging diversity)

Equal Employment Opportunity (EEO)

It is the policy of Gilead Sciences, Inc. and its subsidiaries and affiliates (collectively "Gilead" or the "Company") to recruit select and employ the most qualified persons available for positions throughout the Company. Except if otherwise provided by applicable law, all employment actions relating to issues such as compensation, benefits, transfers, layoffs, returns from layoffs, company-sponsored training, education assistance, social and recreational programs are administered on a non-discriminatory basis (i.e. without regard to protected characteristics or prohibited grounds, which may include an individual’s gender, race, color, national origin, ancestry, religion, creed, physical or mental disability, marital status, sexual orientation, medical condition, veteran status, and age, unless such protection is prohibited by federal, state, municipal, provincial, local or other applicable laws). Gilead also prohibits discrimination based on any other characteristics protected by applicable laws.

For Current Gilead Employees and Contractors Please apply via the Internal Career Opportunities portal in Workday.

Sr. CTM Associate in Uxbridge employer: Gilead Sciences Europe Ltd.

Kite, a Gilead Company, is an exceptional employer that fosters a collaborative and inclusive work culture, dedicated to the development of innovative cancer immunotherapies. Employees benefit from comprehensive training and growth opportunities within a dynamic environment that prioritises integrity, teamwork, and excellence. Located in a vibrant area, Kite offers a unique chance to contribute to groundbreaking clinical trials while enjoying a supportive atmosphere that values diversity and personal accountability.
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Contact Detail:

Gilead Sciences Europe Ltd. Recruiting Team

StudySmarter Expert Advice 🤫

We think this is how you could land Sr. CTM Associate in Uxbridge

✨Tip Number 1

Network like a pro! Reach out to your connections in the biopharmaceutical field, especially those who have experience with clinical trials. A friendly chat can lead to insider info about job openings or even a referral.

✨Tip Number 2

Prepare for interviews by brushing up on your knowledge of CAR-T cell therapy and oncology. We want you to be able to discuss relevant topics confidently, showing that you're not just a fit for the role but also passionate about the work.

✨Tip Number 3

Don’t underestimate the power of follow-ups! After an interview, send a quick thank-you email to express your appreciation. It keeps you fresh in their minds and shows your enthusiasm for the position.

✨Tip Number 4

Apply through our website! It’s the best way to ensure your application gets seen by the right people. Plus, it shows you’re serious about joining our team at Kite, a Gilead Company.

We think you need these skills to ace Sr. CTM Associate in Uxbridge

Clinical Trial Management
Oncology Knowledge
CAR-T Cell Therapy Knowledge
Regulatory Compliance
SOP Familiarity
Communication Skills
Interpersonal Skills
Presentation Skills
Time Management
Organisational Skills
Prioritisation Skills
Proficiency in Word, PowerPoint, and Excel
Knowledge of FDA and EMEA Regulations
ICH Guidelines
GCP Knowledge

Some tips for your application 🫡

Tailor Your CV: Make sure your CV is tailored to the Sr. CTM Associate role. Highlight your relevant experience in clinical trials, especially in oncology and CAR-T cell therapy, as this will catch our eye!

Craft a Compelling Cover Letter: Your cover letter should tell us why you're passionate about clinical research and how your skills align with our values at Kite. Be genuine and let your personality shine through!

Showcase Your Skills: We love seeing candidates who can communicate effectively and manage their time well. Use specific examples in your application to demonstrate these skills, especially in relation to working with CROs and study management.

Apply Through Our Website: Don’t forget to apply through our website! It’s the best way for us to receive your application and ensures you’re considered for the role. We can’t wait to see what you bring to the table!

How to prepare for a job interview at Gilead Sciences Europe Ltd.

✨Know Your Stuff

Make sure you brush up on your knowledge of CAR-T cell therapy and oncology. Familiarise yourself with the latest developments in cancer immunotherapies, as well as Gilead's specific products and trials. This will show that you're genuinely interested and informed about the field.

✨Showcase Your Experience

Be ready to discuss your previous clinical trial experience, especially any roles you've had with CROs or in pharmaceutical companies. Highlight specific examples where you’ve contributed to study management or compliance with regulatory guidelines, as this is crucial for the role.

✨Communication is Key

Since the role involves liaising with various teams, practice articulating your thoughts clearly and concisely. Prepare to demonstrate your interpersonal skills through examples of past teamwork or presentations, as effective communication is essential in this position.

✨Ask Insightful Questions

Prepare thoughtful questions about the company's culture, the Clinical Operations team, and how they ensure compliance with SOPs and regulations. This not only shows your interest but also helps you gauge if the company aligns with your values, especially regarding integrity and teamwork.

Sr. CTM Associate in Uxbridge
Gilead Sciences Europe Ltd.
Location: Uxbridge

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