![Building A Digital PR Strategy: 10 Essential Steps for Beginners [With Examples]](https://buzzsumo.com/wp-content/uploads/2023/09/Building-A-Digital-PR-Strategy-10-Essential-Steps-for-Beginners-With-Examples-bblog-masthead.jpg)
![How Human Behavior Impacts Your Marketing Strategy [Video]](https://contentmarketinginstitute.com/wp-content/uploads/2025/03/human-behavior-impacts-marketing-strategy-cover-600x330.png?#)
![How to Make a Content Calendar You’ll Actually Use [Templates Included]](https://marketinginsidergroup.com/wp-content/uploads/2022/06/content-calendar-templates-2025-300x169.jpg?#)
![How to Use GA4 to Track Social Media Traffic: 6 Questions, Answers and Insights [VIDEO]](https://www.orbitmedia.com/wp-content/uploads/2023/06/ab-testing.png)
Clinical Site Start-Up Lead
A company is looking for a Clinical Site Identification and Start-Up Lead to oversee and manage the end-to-end process of site identification, selection, and start-up activities for clinical trials. Key Responsibilities Lead the site identification and feasibility process for clinical trials, ensuring the selection of qualified sites Oversee site start-up activities including contract negotiations, regulatory document collection, and site initiation visits Continuously identify opportunities for process improvements to streamline site identification and start-up timelines Required Qualifications Bachelor's degree in Life Sciences, Clinical Research, or a related field Minimum of 2 years of experience in clinical trials with a focus on site identification or start-up Experience with regulatory submissions and site initiation processes is essential Strong knowledge of clinical trial regulations and ICH-GCP guidelines Familiarity with clinical trial management systems (CTMS) and electronic data capture (EDC) platforms
A company is looking for a Clinical Site Identification and Start-Up Lead to oversee and manage the end-to-end process of site identification, selection, and start-up activities for clinical trials.
Key Responsibilities
Lead the site identification and feasibility process for clinical trials, ensuring the selection of qualified sites
Oversee site start-up activities including contract negotiations, regulatory document collection, and site initiation visits
Continuously identify opportunities for process improvements to streamline site identification and start-up timelines
Required Qualifications
Bachelor's degree in Life Sciences, Clinical Research, or a related field
Minimum of 2 years of experience in clinical trials with a focus on site identification or start-up
Experience with regulatory submissions and site initiation processes is essential
Strong knowledge of clinical trial regulations and ICH-GCP guidelines
Familiarity with clinical trial management systems (CTMS) and electronic data capture (EDC) platforms