Clinical Trial Administrator

Company Overview:

We are partnered with an independent Clinical Research Organisation (CRO) dedicated to delivering high-quality Clinical Trial services. They collabroate with niche biotech and pharma sponsors and so offer some unique and complex project work.

Over recent years they have seen some healthy growth and are continuing to grow their clinical teams coming into 2024. They are hiring for two Clinical Trial Administrators to help support the project team on a varity of innovative clinical studies.

You will be joining a genuinely close and supportive team that push for a collaborative environment where every team member's contribution is valued. If you're passionate about clinical research and eager to learn from industry professionals in a close-knit team setting, this is the perfect opportunity for you.

Key Responsibilities:

• Assist in the coordination and management of Clinical Trial activities according to protocols, timelines, and regulatory requirements.
• Prepare and maintain essential trial documentation, including study files, informed consent forms, and regulatory submissions.
• Facilitate communication between study sites, investigators, sponsors, and internal team members.
• Coordinate site initiation, monitoring, and close-out visits, ensuring compliance with protocols and standard operating procedures (SOPs).
• Manage study supply inventory and distribution, tracking shipments and maintaining documentation.
• Support data management activities, including data entry, query resolution, and database maintenance.
• Contribute to the development and implementation of process improvements to enhance efficiency and quality in Clinical Trial operations.
• Participate in team meetings, training sessions, and professional development opportunities to expand knowledge and skills in clinical research.

Qualifications:

• Bachelor's degree in life sciences, healthcare, or a related field.
• Previous experience in clinical research or healthcare administration preferred but not required.
• Excellent communication and interpersonal abilities.
• Proficiency in Microsoft Office suite (Word, Excel, Outlook).

They will be holding interviews in the coming weeks and so do not hesitate to apply. For more information please contact Keeley Munday at ******@i-pharmconsulting.com