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The Role The Clinical Trial Administrator, is responsible to provide administrative support for the Project Management group and to lead the study review activities and communications on allocated projects To comply & adhere to GCP guidelines and regulations as required of this role Main Tasks and R

The Role This is an exciting opportunity to take ownership of synthesis projects from planning through to delivery, working in line with company procedures and regulatory requirements including GMP and IRR17. You’ll also play a key client-facing role, representing the IL team in project meetings and

The Role Responsible for coordinating, supervising and monitoring study activities, following adverse events and administering study medications To comply & adhere to GCP guidelines and regulations as required of this role To ensure study data is collected to a high quality in accordance with Good C

The Role Responsible for controlling the Inventory area, processing all purchase orders for the clinical and facilities departments. Responsible for ordering, receiving, distributing supplies around the Miami site, Screening Location, maintaining the inventory system, sourcing and ordering goods on

Are you an experienced analytical laboratory professional with a strong eye for detail and a passion for data quality? This is an opportunity to use your analytical knowledge in a role where you'll play an important part in ensuring laboratory data is accurate, complete and compliant. You'll work cl

The Role The purpose of this position is to install, repair and maintain facilities equipment and systems including the physical facility. Provides courier services for all Miami site facilities To ensure volunteer safety at all times including the following of social distancing practices and proced

The Role Responsible for the following data entry associated tasks for their assigned studies: source document retrieval, source data QC, data entry, source document filing, QC of CRF entries, laboratory result tracking, and archiving To comply & adhere to GCP guidelines and regulations as required

Remote - West Coast, United States | Up to 50% Travel | Full-Time | Exempt Accelerate Drug Development. Shape the Future of Pharmaceutical Innovation. At Quotient Sciences, we're redefining how medicines reach patients. As a leading CRDMO (Contract Research, Development and Manufacturing Organizatio

The Role At Quotient Sciences, everyday counts when bringing new medicines to patients. As a Formulation Scientist, you'll play an important role in transforming promising drug candidates into pharmaceutical products suitable for clinical development. Working within our Formulation Development team,

The Role The Clinical Laboratory Technician is responsible for following protocol guidelines for the preparation, collection, transfer and storage of all specimens according to protocol requirements Monitors proper study sample collection Ensures study data is collected to a high quality in accordan

The Role Responsible for coordinating, supervising and monitoring study activities, following adverse events and administering study medications To comply & adhere to GCP guidelines and regulations as required of this role To ensure study data is collected to a high quality in accordance with Good C

About the Role This is a 12 month fixed term contract We are seeking a highly organised and proactive Drug Product Coordinator to support the successful delivery of drug product manufacturing activities across a diverse range of client projects. This role is critical in ensuring manufacturing operat

Are you a confident communicator with a passion for helping people and delivering a positive experience? As a Recruitment Assistant (Volunteer Recruiter), you will play a key role in supporting the successful recruitment and scheduling of research volunteers for clinical studies. Working as part of

The Role Arcinova, a Quotient Sciences company, is seeking a Head of Drug Product to lead our Drug Product Manufacturing and Formulation Development teams based at our Alnwick site. In this role, you will lead, engage, develop and coach teams of manufacturing and formulation scientists to ensure the

Do you enjoy helping people, building positive relationships, and creating an exceptional experience for others? As a Research Volunteer Liaison (Activities Coordinator), you will play a key role in supporting volunteers throughout their clinical trial journey. Working closely with our Clinical and

The RoleLead the planning and delivery of customer and internal projects at our Alnwick site, ensuring timelines, budgets, and quality standards are consistently met. Acting as the central point of contact, you will build strong relationships with clients and internal teams, keeping projects on trac

*Hiring for full-time and per diem schedules* The Role Collects biological samples, performs phlebotomy, vital signs and ECG’s in accordance with the specific activity schedule. Tracks overall study event schedule and participant compliance. To ensure study data is collected to a high quality in acc

The Role Collects biological samples, performs phlebotomy, vital signs and ECG’s in accordance with the specific activity schedule. Tracks overall study event schedule and participant compliance. To ensure study data is collected to a high quality in accordance with Good Clinical Practice (GCP) stan