At a Glance
- Tasks: Support clinical projects from start to finish, ensuring quality and timely delivery.
- Company: Join Quotient Sciences, a leader in innovative medicine development.
- Benefits: Gain hands-on experience, work with industry experts, and develop your skills.
- Other info: Dynamic team environment with opportunities for growth and learning.
- Why this job: Make a real difference in bringing medicines to patients faster.
- Qualifications: Degree in life sciences and strong organisational skills required.
The predicted salary is between 30000 - 40000 £ per year.
The Role At Quotient Sciences, you'll play a key role in helping bring innovative medicines to patients faster.
Working within a collaborative, fast-paced project management environment, you will support the successful delivery of clinical projects from start to finish, ensuring they are completed to the highest quality standards, on time and within budget.
This is an excellent opportunity to gain broad exposure across project management, clinical operations and client delivery while working alongside experienced industry professionals.
Main Tasks and Responsibilities
Support the preparation, production and formatting of key study documentation, including informed consent forms, training materials, file notes and laboratory manuals.
Assist with the selection, set-up and management of external vendors to support project delivery.
Support internal risk-based monitoring activities following first patient dosing, helping to ensure study processes and documentation are operating effectively.
Contribute to the generation of project data and reports, including recruitment updates, adverse event summaries and study metrics.
Coordinate and host Sponsor monitoring visits, ensuring a professional and positive client experience.
Support Project Managers with study close-out activities, including archiving, reconciliation and project documentation management.
Assist with the resolution and tracking of data queries to support study progress and data quality.
Contribute to continuous improvement initiatives, helping to enhance processes, efficiencies and ways of working.
Work closely with cross-functional study teams to ensure Investigator Site Files (ISF) and Trial Master Files (TMF) are maintained to the highest standards.
Provide broader support to the Commercial and Project Management teams, contributing to both the winning and delivery of exciting client projects.
Qualifications and Experience Required
Degree qualified (or equivalent) in a life sciences or related discipline.
Previous experience within a pharmaceutical company, CRO or clinical research environment would be advantageous.
Strong organisational skills with excellent attention to detail.
Ability to manage multiple priorities in a dynamic and collaborative environment.
Excellent communication skills and a proactive, team-focused approach.
Clinical Project Coordinator in Nottingham employer: Quotient Sciences
Quotient Sciences is an exceptional employer located in Nottingham, offering a dynamic work environment that prioritises volunteer safety and compliance in clinical research. With a strong focus on professional development and leadership opportunities, employees are encouraged to grow their careers while contributing to meaningful advancements in medical solutions. Join us to be part of a collaborative culture that values innovation and excellence in healthcare.
