Job Description A large Philadelphia-based hospital is seeking a Clinical Trials Study Start-Up Project Manager to join their team. This role is 100% onsite for the first 90 days, transitioning to a hybrid schedule thereafter. Working on 15-30 studies in active startup/feasility questionnaire. Key Responsibilities - Coordinate all clinical aspects of study start-up activities - Manage timelines and ensure adherence to project milestones - Facilitate communication and collaboration among team members - Track study progress and maintain accurate documentation - Complete feasibility questionnaires and submit to sponsors - Coordinate scheduling for pre-site visits, including equipment and supply needs in collaboration with the Principal Investigator (PI) - Route study protocols to internal committees for review - Liaise with CROs and sponsors throughout the start-up phase We are a company committed to creating inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity employer that believes everyone matters. Qualified candidates will receive consideration for employment opportunities without regard to race, religion, sex, age, marital status, national origin, sexual orientation, citizenship status, disability, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to Human Resources Request Form (https://airtable.com/app21VjYyxLDIX0ez/shrOg4IQS1J6dRiMo) . The EEOC "Know Your Rights" Poster is available here (https://www.eeoc.gov/sites/default/files/2023-06/22-088\_EEOC\_KnowYourRights6.12ScreenRdr.pdf) . To learn more about how we collect, keep, and process your private information, please review Insight Global's Workforce Privacy Policy: https://insightglobal.com/workforce-privacy-policy/ . Skills and Requirements - Experience with clinical trisl study start up - Managing the study start up process -> workflows and timelines - 5 years of clinical trials study start up experience with bachelors degree or 3 years of clinical trials study start up experience with a masters degree - Phase I clinical trials experience null We are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal employment opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment without regard to race, color, ethnicity, religion,sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military oruniformed service member status, or any other status or characteristic protected by applicable laws, regulations, andordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or the recruiting process, please send a request to HR@insightglobal.com.