Job Title: Senior Clinical Project Manager

Location: London Bridge, SE1

Term: Permanent, Full-time

Salary: Competitive + Benefits (Private Medical, Private Dental, Pension, 25 days Annual leave plus bank holidays & Many more)

Richmond Pharmacology are an early phase Clinical Research Organisation (CRO), where we are conducting pioneering early phase healthy participants and patient participant trials. Our experienced and world-renowned team, our central London location and our global reach contribute to making Richmond Pharmacology an exciting and dynamic place to work.

Purpose Of The Job

The Senior Clinical Project Manager is responsible for managing the trial from set-up through to the clinical and post-clinical phases, overseeing the operational delivery of our clinical trials. This involves coordinating the activities of cross-functional teams and closely interfacing with internal departments and external stakeholders to ensure the highest level of output from each trial. The Senior Clinical Project Manager is held accountable for achieving the successful delivery of budgeted activities at the project level, adhering to company and regulatory requirements within specified time, quality/scope, and budget constraints.

They must ensure that the trials are conducted in accordance with the protocol, Standard Operating Procedures (SOPs), Good Clinical Practice (GCP), and other local regulatory requirements.

Main Duties And Responsibilities

• To perform, manage, and coordinate the setup and running of clinical trials in accordance with the protocol, Richmond SOPs, GCP, and all relevant guidelines.
• Acting as the main point of contact for sponsors, vendors, and the wider project team.
• Ability to help with trial design by liaising directly with sponsors and PI, integrate information from a range of sources and critically evaluate it, identify the implications and making appropriate decisions (e.g. about study design and timing).
• Quality check and coordinate flow of all study documents, ahead of study initiation.
• Check meeting agendas, minutes, documents, and scheduling.
• Coordinate external and internal study meetings, as required.
• Supervise/mentor CRS and CPMs within teams, as required.
• Maintain and quality control the Investigator Site File.
• Ensure effective close out activities.
• Manage resolution of data queries to facilitate timely database lock and reviews of study reports, ahead of submission to regulatory authority.
• Undertake continuous improvement activities in relation to further improving processes and work culture.
  
  

Skills And Experience

• BSc in Life Sciences (or equivalent); or other clinical research academic qualification (e.g., MSc, Post Grad Diploma etc.)
• Previous experience working in a Clinical Project Management position
• Ability to communicate professionally and appropriately with external clients and internal professionals.
• Excellent communication skills, both written and verbal.
• Strong fundamental knowledge in project management methodologies, principles and demonstrable practical exposure.
  
  

Application

If you are interested in the role, please register your details, including a copy of your CV. Please note, while we try to respond to every candidate, the high volume of applications anticipated may make this impossible and we ask for your patience and understanding.