Site Engagement Lead

Structure Therapeutics

6d•$152,000 - $205,000•Hybrid

About The Position

Structure Therapeutics develops life-changing medicines for patients using advanced structure-based and computational drug discovery technology. The company’s platform combines the latest advancements in visualization of molecular interactions, computational chemistry, and data integration to design orally available, superior small molecule medicines that overcome current limitations of biologic and peptide drugs. We are advancing a clinical-stage pipeline of differentiated treatments focused on chronic diseases with high unmet need, including cardiovascular, metabolic, and pulmonary conditions. Structure Therapeutics is led by an experienced group of international drug innovators and financed by top-tier global life sciences investors. The company completed an initial public offering (IPO) in February 2023. With offices in California and Shanghai, Structure Therapeutics has the benefit of being at the center of life science innovation in both the US and China and capitalizing on the strengths of each geographic location. Position Summary: Reporting to the Director, Clinical Development and Site Engagement, this position will be responsible for supporting overall participant recruitment and retention. This position works closely with research coordinators, investigators, and study teams to provide participant support, address site level concerns, and implement engagement strategies and trial education that encourage continued participation in clinical studies. The Site Engagement Lead (Clinical) will share ideas and planning with trial teams to optimize participant recruitment and retention, driving engagement of the right participants, ones that are willing and capable of performing the protocol specified visit schedule and tasks associated with their study participation to completion.

Requirements

NP-C/PA-C/BSN/Master of Science preferred with a minimum of 8 years of relevant experience (includes Site, SMO, CRO, and/or Sponsor).
Deep understanding of the clinical trial process and the ability to develop and implement successful recruitment and retention strategies
Strong analytical skills with experience in understanding trial metrics, analyzing trends and adjusting to meet goals in a fast-paced environment
Excellent communication and interpersonal skills with a patient-centered approach
Capable of managing multiple timelines while working with cross-functional groups
Attention to detail and organizational

Nice To Haves

Studies in Dietetics or Nutrition, along with experience in chronic weight management with GLP1s is a plus

Responsibilities

Support the design and execution of patient recruitment, collaborating with study teams to identify the target population and support outreach strategies across the trials.
Develop and implement study plans for recruitment and retention.
Develop and implement educational plans and tools for sites to aid in protocol execution and participant safety.
Building and maintaining relationships with sites, CROs, and vendors that support trial recruitment and retention efforts.
Extend the company connection to advocacy groups and other organizations that support recruitment and retention in clinical trials.
Conduct market research to understand patient needs and barriers to participation in clinical trials and using this information to plan adequate recruitment/retention strategies.
Create Site and Participant facing documents/materials that define direction and support of recruitment and/or retention.