We are looking for a Clinical Project Manager to become a team member for local and international clinical studies reporting to a senior project manager.
Brief Job Description:
The candidate will be responsible for conducting clinical studies, managing & monitoring study sites in accordance with Study Protocols, SOPs, ICH-GCP (International Clinical Harmonization-Good Clinical Practice) and local regulations. She/he will manage multiple projects, support Project Teams.
She/he will also be responsible for coordinating all necessary activities required to set up a study, participating in the start-up processes including reviewing protocols, reviewing Case Report Forms (CRFs), preparing Informed Consent Forms (ICFs), developing study documents, organizing investigator and study specific training meetings, presenting study related material and ensuring that the study meets planned timelines and high quality data is generated.