audits within the department.
This role will play a key role in bringing deep clinical understanding and judgment in benefit-risk assessments role will also ensure projects adhere to Good Clinical and Pharmacovigilance Practice and Regulatory interpretation of safety information collected from pre-clinical through to post-marketing, including medical review Investigator's Brochures, Clinical Study Protocol, Study Safety Plans, and Clinical Safety reports. Reviewing PV and medical information activities. Develop/ educate employees. Support the growth of new PV business
This role will play a key role in bringing deep clinical understanding and judgment in benefit-risk assessments role will also ensure projects adhere to Good Clinical and Pharmacovigilance Practice and Regulatory interpretation of safety information collected from pre-clinical through to post-marketing, including medical review Investigator's Brochures, Clinical Study Protocol, Study Safety Plans, and Clinical Safety reports. Reviewing PV and medical information activities. Develop/ educate employees. Support the growth of new PV business
internal audits within the department. Assist in facilitating third-party audits as instructed by the department for enhancing the quality management system and facilitate necessary actions. Provide regulatory support including assisting in technical documentation and clinical evaluations. Deliver and coordinate training on
and in report format. Stakeholder Management Facilitate and manage communication with relevant internal
and in report format. Stakeholder Management Facilitate and manage communication with relevant internal
and potential areas for improvement - Train and educate staff on quality control procedures - Maintain
and potential areas for improvement - Train and educate staff on quality control procedures - Maintain