Clinical Trials Assistant

PA 2 Assist Ltd.; Wolverhampton; On-site; GBP 25,000 - 35,000; Full time

Job summary

A clinical study support company based in Wolverhampton is seeking candidates for a role involving the implementation of clinical studies. Responsibilities include monitoring data, ensuring compliance with protocols, and supporting multiple studies on tight timelines. The ideal candidate should possess a Bachelor's degree in relevant fields and be proficient in applications like Outlook and Excel. Previous experience in clinical studies is preferred to further enhance the team’s efficiency and effectiveness.

Qualifications

• Support multiple clinical studies and prioritize tasks under tight timelines.
• Maintains relationships with stakeholders, both internal and external.
• Knowledge of Good Clinical Practice (GCP) preferred.

Responsibilities

• Participate in set-up and implementation of clinical studies.
• Ensure required devices and materials for the study are available.
• Monitor clinical study data to ensure compliance with protocols.
• Assist in audits and regulatory inspections as needed.

Skills

Relationship management

Time management

Data analysis

Software proficiency (Outlook, Word, Excel, PowerPoint)

Education

Bachelor's degree in relevant studies

Job description

JOB DETAILS

Let's talk about the role:

• Participates in the set-up and implementation of clinical studies through communication between the CDS and the study site.
• Supports the CDS to ensure that all required devices and materials for the study are prepared and available
• Ensures the clinical study database and Case Report Forms (CRFs) are prepared in advance of the study commencing
• Assist in monitoring of the clinical study data during the conduct of the study to ensure compliance to the study protocol and applicable Work Instructions
• Assists in audits and Regulatory Inspections as required
• Verifies study documentation files and finalises the study closure reports at the completion of the clinical study
• Appropriately documents and archives study data and documentation as per Work Instructions following the completion of the clinical study

Let's talk about you:

Required:

• Bachelor's degree in relevant studies
• Ability to support multiple clinical studies on relatively tight timelines and prioritise multiple tasks
• Developing and maintaining relationships with internal and external stakeholders
• Follows standard practices and procedures and applies basic theories, concepts, principles and methodologies in analyzing situations or data
• Receives instruction, guidance and direction from others.
• Proficient in software applications such as Outlook, Word, Excel and PowerPoint

Preferred:

• Previous experience in the conduct of clinical studies
• Knowledge of Good Clinical Practice (GCP), ISO 14155, and other guidelines and Standards as appropriate

Are you interested in this position?

Apply by clicking on the “Apply Now” button below!

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