Senior Clinical Trial Associate

Catalyst Clinical Research; Santander; Presencial; EUR 40.000 - 60.000; Jornada completa

Descripción de la vacante

Catalyst Clinical Research is hiring a Senior Clinical Trial Associate in Santander, Spain. The role involves providing administrative support to clinical project teams, overseeing clinical trial documentation, and ensuring compliance with ICH-GCP standards. Applicants should have a degree in life sciences or nursing and 2+ years of relevant experience.

Formación

• 2+ years’ experience in clinical trial processes and procedures.
• Experience in maintaining Trial Master Files compliant with ICH-GCP.

Responsabilidades

• Support clinical trial activities concerning time, cost, and quality.
• Maintain documentation folders and Trial Master Files.
• Serve as a contact point for all sites during the trial.

Conocimientos

Understanding of ICH-GCP

Clinical research experience

Communication skills

Organisational skills

Technical skills (PowerPoint, Excel, Word)

Educación

Degree in life sciences or nursing

Descripción del empleo

Catalyst Clinical Research provides customizable solutions to the biopharmaceutical and biotechnology industries through Catalyst Oncology , a full-service oncology CRO,andmulti-therapeutic global functional and CRO services through Catalyst Flex . The company's customer-centric flexible service model, innovative technology, expert team members, and global presence advance clinical studies. Visit CatalystCR.com .

As a SeniorClinical Trial Associate you are responsible for providing the administrative support to the clinical development / project teams and maintaining a range of clinical documentation. You will be focused on supporting external client teams as well as our internal Clinical Services team. Youwill work closely with project teams to ensure that Clinical Trial Administration is performed in line with ICH-GCP allowing successful delivery of trials whilst protecting subjects’ rights, safety and wellbeing and the production of reliable clinical trial data.

Position Accountabilities / Responsibilities :

• Support the clinical trial activities with regard to time, cost and quality and in accordance with SOPs, ICH-GCP guidelines and relevant regulations
• Set up and maintain the documentation folders associated with product development and the Trial Master File (TMF) in compliance with ICH-GCP
• Ensure the TMF index is kept up to date
• Coordinate the collection of essential documents during site set-up
• Assist in the development of processes and procedures in order to ensure that robust forecasting and scheduling of trials occurs
• Assist the project managers in the production of study reports and updates as required
• Set up trial specific meetings, taking minutes and tracking screening and enrolment across clinical sites
• Track and process investigator site payments
• Manage the clinical trial supplies for a study, including the tracking and shipment of materials e.g. lab kits
• Assists the project team with preparation and shipment of Clinical Trial documentation including : Investigator Site File, Pharmacy File, Investigator Brochure, Protocol and study manuals.
• Update and maintain trial tracking systems in accordance to the demands of the study e.g. investigational product tracking, payment tracking, monitoring visit tracking etc.
• Serve as an office-based point of contact for all sites during the trial
• Develop and maintain good working relationships with Investigators and study staff
• Assist with corporate administration activities according to need and availability

Position Qualifications and Requirements :

Education : Degree or equivalent qualification in life sciences or nursing

Experience :

• 2+ years’ experience in clinical trial processes and procedures including regulatory standards

Required Certifications : N / A

Required Skills :

• A good understanding of ICH-GCP and regulatory requirements
• Proven track record in working within clinical research in the pharmaceutical, CRO or NHS environment
• Experience in maintaining Trial Master Files / Investigator Site Files in compliance with ICH-GCP (ideally experience in using the DIA reference model).
• Ability to work collaboratively with others, influencing and managing conflict
• Willingness and ability to travel domestically (and occasionally internationally) as required
• Excellent verbal and written communication and interpersonal skills
• Strong organisational and time management skills with an ability to multi task and work independently
• Strong technical skills using PowerPoint, Excel and Word

Working Conditions : Sedentary work that primarily involves sitting / standing. Employee may be office or home based.

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