Clinical Support Professional - TMF & PV

We are looking for a highly skilled and experienced professional to join our team as a Clinical Support - TMF & PV specialist. The ideal candidate will have a strong background in the Pharmaceutical & Life Sciences industry, with expertise in clinical support, TMF, and PV.

Roles and Responsibility

• Provide clinical support for trials, including data review and reconciliation.
• Manage and maintain trial management files (TMF) according to regulatory requirements.
• Conduct patient visits and site monitoring activities to ensure compliance with study protocols.
• Collaborate with cross-functional teams to resolve issues and improve processes.
• Develop and implement quality control procedures to ensure high-quality data.
• Participate in process improvement initiatives to enhance efficiency and effectiveness.

Job Requirements

• Bachelor's degree in a relevant field, such as life sciences or pharmacy.
• Proven experience in clinical support, preferably in a pharmaceutical company setting.
• Strong knowledge of Good Clinical Practice (GCP), International Conference on Harmonisation (ICH) guidelines, and other relevant regulations.
• Excellent communication and interpersonal skills, with the ability to work effectively with stakeholders at all levels.
• Proficient in using computer systems, including electronic health records and other software applications.
• Ability to work in a fast-paced environment, prioritizing multiple tasks and meeting deadlines.