Clinical Trials Associate

Britannia Pharmaceuticals Ltd; Reading; Hybrid; GBP 30,000 - 50,000; Full time

Job summary

Join a leading pharmaceuticals company as a Clinical Trials Associate, responsible for the global execution of clinical studies. This role offers an opportunity to impact healthcare significantly through effective project management, compliance oversight, and collaboration with various stakeholders, all within an innovative team environment.

Benefits

Green Park events programme

Electric Car Scheme

Long Service Awards

Eye Care Vouchers

Salary Sacrifice Pension Scheme

25 days annual leave plus bank holidays

Wellbeing support through Employee Assistance Programme

Qualifications

• Prior experience in clinical development with knowledge of Clinical Operations.
• Solid understanding of regulatory processes and quality requirements.
• Experience managing CROs is advantageous.

Responsibilities

• Oversee execution and delivery of clinical studies according to defined protocols.
• Manage project-related expenses and site payment processes.
• Coordinate monitoring from site activation to study closure.

Skills

Project Management

Collaboration

Communication

Negotiation

Problem Solving

Education

Scientific degree in life sciences or equivalent

Job description

Join to apply for the Clinical Trials Associate role at Britannia Pharmaceuticals Ltd

Join to apply for the Clinical Trials Associate role at Britannia Pharmaceuticals Ltd

Direct message the job poster from Britannia Pharmaceuticals Ltd

Are you passionate about clinical research and looking to make a significant impact in the healthcare industry? Britannia Pharmaceuticals is seeking a dedicated Clinical Trials Associate to join our dynamic team. In this role, you will be responsible for the global execution and timely delivery of assigned studies across various therapy areas, ensuring adherence to quality, budget, and regulatory standards.

Key Responsibilities:

• Study Management: Oversee execution and delivery of clinical studies according to the defined protocols while ensuring compliance with local regulations, ICH GCP, and Britannia’s standards.
• Leadership: Collaborate with the Medical Affairs Manager to drive study conduct decisions and escalate issues when needed.
• Project Coordination: Manage country and site-level activities, including site management, monitoring activities, and ensuring timely report reviews.
• Stakeholder Liaison: Be the operational point-of-contact for internal teams, CROs, and clinical site staff to facilitate effective communication and collaboration.
• Process Improvement: Identify and implement best practices, ensuring optimal performance of study teams while maintaining regulatory compliance.
• Site Selection: Assist in identifying potential study sites and conducting Site Quality Risk Assessments in collaboration with local Affiliates.
• Regulatory Submissions: Ensure timely submission of all necessary documents to Ethics Committees and Regulatory Authorities throughout the study lifecycle.
• Financial Management: Manage project-related expenses, perform budget reconciliations, and oversee site payment processes.
• Documentation Oversight: Collect and verify essential trial documents to ensure compliance with ICH GCP requirements before study initiation.
• Monitoring Activities: Coordinate monitoring from site activation to study closure, ensuring adherence to Monitoring Plans.
• Risk Management: Develop and maintain a global risk management plan to proactively identify and mitigate risks associated with sites and stakeholders.
• Meeting Coordination: Plan and lead Investigator meetings in accordance with local regulations.

Personal Specification (Skills Required)

• Education: Scientific degree or equivalent experience in life sciences, clinical research, pharmacy, or related field.
• Experience: Prior experience in clinical development, with extensive knowledge in Clinical Operations and experience managing CROs.
• Knowledge: Solid understanding of clinical research management, regulatory processes, and quality requirements.
• Strong project management and team collaboration abilities.
• Excellent written and verbal communication skills in English.
• Strong negotiation skills and effective problem-solving capabilities.

What we can offer you!

️Green Park offer 500+ events programme – free workout classes, beekeeping & more!

Electric Car Scheme – save up to 40% on the monthly cost, thanks to savings on national insurance and income tax

Long Service Awards – additional annual leave and bonus

Eye Care Vouchers

Salary Sacrifice Pension Scheme

Hybrid working – we spend three days in the office, with Wednesday and Friday as working at home.

25 days of annual leave plus bank holidays. Additional leave given on your birthday month (wellbeing leave)

Wellbeing support through our Employee Assistance Programme and KYAN Wellbeing – offering free coaching and counselling services for you and your family.

Plus, many more employee benefits & celebration events across the year.

Application Requirements

We are regrettably unable to accept applications from candidates who do not have the right to work in the UK or require sponsorship to work in the UK.

Seniority level

• Seniority level

  Associate

Employment type

• Employment type

  Full-time

Job function

• Job function

  Project Management and Other

• Industries

  Pharmaceutical Manufacturing

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