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- Tasks: Manage and deliver clinical trials while ensuring compliance with protocols and regulations.
- Company: Join Accession Therapeutics, an innovative biotech company in Oxford focused on early-phase clinical research.
- Benefits: Enjoy a competitive salary, pension, private health insurance, life insurance, and gym membership discounts.
- Why this job: Be part of a dynamic team making a real impact in healthcare and biotechnology.
- Qualifications: 5+ years in a relevant role, strong communication skills, and experience in clinical trial documentation.
- Other info: Opportunities for site visits and cross-functional collaboration; biotech experience preferred.
The predicted salary is between 36000 - 60000 £ per year.
Accession Therapeutics Limited, a vibrant, early-phase biotechnology company based in Oxford, is looking for a Clinical Study Manager/Senior Clinical Study Manager to assist with the set-up, management and delivery of the company’s clinical trials in compliance with study protocols and GCP and regulatory standards. You will join a small Clinical Operations team, working closely with the Medical Director, Quality, CMC and Translational Medicine teams; activities will be commensurate with experience.
RESPONSIBILITIES TO INCLUDE:
- Daily interaction and collaboration with CROs and third-party vendors delivering the clinical trials;
- Liaising with study sites to support clinical trial delivery, efficiency and data integrity;
- Maintenance and management of clinical trial documentation;
- Tracking site performance, budgets and sample management;
- Providing additional support, as required.
CANDIDATE WILL NEED:
- Good educational background; at least 5+ years’ experience working in a relevant role;
- Good communication and presentation skills;
- Experience at writing clinical trial documentation;
- Willingness to make occasional study site visits, as required;
- Ability to work effectively in cross-functional teams;
- Understanding of the requirements of relevant regulatory and healthcare bodies;
- Willingness to undertake additional activities to support other departments;
- Experience of or willingness to learn Data Management or Pharmacovigilance and become the SME;
- Biotech experience (preferred);
- Experience of early-phase oncology and ATMP (preferred).
Accession offers a good salary and company benefits including pension, private health insurance, life insurance and subsidised local gym membership.
To apply for this position please send a LETTER OF APPLICATION (essential) and a COPY of your C.V. to joinus@accessiontherapeutics.com.
Any personal data that is sent in connection with applications will be used by us in accordance with our privacy policy here.
CLINICAL STUDY MANAGER /SENIOR CLINICAL STUDY MANAGER employer: Accession Therapeutics Limited
Contact Detail:
Accession Therapeutics Limited Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land CLINICAL STUDY MANAGER /SENIOR CLINICAL STUDY MANAGER
✨Tip Number 1
Familiarise yourself with Good Clinical Practice (GCP) guidelines and regulatory standards relevant to clinical trials. This knowledge will not only help you in interviews but also demonstrate your commitment to compliance and quality in clinical research.
✨Tip Number 2
Network with professionals in the biotechnology and clinical research fields, especially those who have experience in early-phase oncology and ATMP. Attend industry conferences or webinars to make connections that could lead to valuable insights and potential referrals.
✨Tip Number 3
Prepare to discuss your experience with cross-functional teams during interviews. Highlight specific examples where you successfully collaborated with different departments, as this is crucial for the role at Accession Therapeutics.
✨Tip Number 4
Show your enthusiasm for the role by researching Accession Therapeutics and their current projects. Being knowledgeable about their work will allow you to ask insightful questions and demonstrate your genuine interest in contributing to their clinical trials.
We think you need these skills to ace CLINICAL STUDY MANAGER /SENIOR CLINICAL STUDY MANAGER
Some tips for your application 🫡
Tailor Your Letter of Application: Make sure to customise your letter of application specifically for the Clinical Study Manager/Senior Clinical Study Manager position. Highlight your relevant experience, particularly in clinical trial management and documentation, and demonstrate your understanding of GCP and regulatory standards.
Showcase Relevant Experience: In your CV, emphasise your 5+ years of experience in a similar role. Include specific examples of your work with CROs, study sites, and any cross-functional teams you've collaborated with. This will help illustrate your capability to manage clinical trials effectively.
Highlight Communication Skills: Since good communication and presentation skills are essential for this role, provide examples in your application that showcase these abilities. Mention any presentations you've delivered or successful collaborations that required strong communication.
Demonstrate Willingness to Learn: If you have experience in Data Management or Pharmacovigilance, be sure to mention it. If not, express your willingness to learn and become a Subject Matter Expert (SME) in these areas. This shows your commitment to professional growth and adaptability.
How to prepare for a job interview at Accession Therapeutics Limited
✨Know Your Clinical Trials
Familiarise yourself with the specifics of clinical trials, especially in early-phase oncology and ATMP. Be prepared to discuss your previous experiences and how they relate to the responsibilities outlined in the job description.
✨Demonstrate Cross-Functional Collaboration
Highlight your ability to work effectively in cross-functional teams. Share examples of past collaborations with different departments, such as Medical, Quality, or CMC, to show that you can thrive in a small team environment.
✨Prepare for Regulatory Questions
Brush up on your knowledge of GCP and regulatory standards relevant to clinical trials. Be ready to discuss how you ensure compliance in your work and any challenges you've faced in maintaining data integrity.
✨Show Enthusiasm for Learning
Express your willingness to learn about Data Management or Pharmacovigilance. Mention any relevant training or courses you've taken, and convey your eagerness to become a subject matter expert in these areas.
