Study Start-Up Manager

Providing operational expertise and customer-focused leadership, the full-time Study Start-Up Manager will oversee start-up and activation activities for multiple studies in a fully remote environment, ensuring compliance with applicable regulations and efficient delivery throughout all phases of start-up. Key responsibilities Manage the operational aspects of study start-up activities across various regions or globally Ensure adherence to Veristat policies, SOPs, and regulatory requirements, including GCP and ICH guidelines Lead and mentor project teams to achieve successful outcomes in clinical operations Required qualifications Bachelor's degree in a relevant field, preferably biological science, Pharmacy, or Nursing 4 to 6 years of experience in Clinical Operations or a similar department SOCRA or ACRP certification and/or membership preferred Thorough knowledge of clinical development processes and regulatory environments Expertise in Microsoft applications and proven experience in leading clinical study operations