Job Title: HEOR Program Manager Job Description The Program Manager - Study Intake is responsible for executing business and administrative processes required for the assessment, review, and initiation of clinical trials and research studies across a minimum of three therapeutic areas, including Cardiovascular, Cancer, Neuroscience, Oncology, and Digestive Health. Responsibilities * Collaborate with business development teams to pursue quality, revenue-generating trials. * Review and route feasibility assessments of proposed research projects, including sponsor collaboration and engagement with site investigators. * Initiate and oversee the Scientific Operational Administrative Review (SOAR) process for incoming projects and gather feedback from key stakeholders. * Assist with regulatory processes to ensure smooth flow of study projects within assigned departments. * Communicate effectively with investigators, scientists, leadership, staff, and external research collaborators. * Review existing research projects for ongoing feasibility and provide updates to business development leads. * Maintain current knowledge of ICH Good Clinical Practices and compliance with local, state, and federal regulations governing human subjects research. * Collaborate with other research departments to ensure regulatory compliance. * Recommend, develop, and update institutional policies and procedures in collaboration with central offices and stakeholders. Essential Skills * Clinical research experience. * Health economics and data analysis expertise. * Deep expertise in study-startup processes, including synopsis reviews and feasibility assessments. * Knowledge of local, state, GCP, and federal regulations governing human subjects clinical trials. * Proficient in Microsoft Office and relevant computer programs. Additional Skills & Qualifications * Excellent interpersonal skills and effective communication with all levels of personnel. * Self-motivated, detail-oriented with good organizational and analytical skills. * Experience in clinical trial operations from execution through completion. * Bachelor's degree in Medical, Scientific, Business, Administration, or related field. * 5 years of experience in a healthcare or research environment OR 3 years of experience in clinical trial operations. Work Environment The role requires sitting in one of the following states: Alabama, Alaska, Arizona, Arkansas, Colorado, Connecticut, Florida, Georgia, Illinois, Indiana, Iowa, Kansas, Louisiana, Maryland, Michigan, Minnesota, Missouri, Montana, Nebraska, New York, North Carolina, Ohio, Oklahoma, Pennsylvania, South Carolina, Tennessee, Texas, Virginia. Pay and Benefits The pay range for this position is $90000.00 - $122000.00/yr. Benefits from Day One Paid Days Off from Day One Student Loan Repayment Program Career Development Whole Person Wellbeing Resources Mental Health Resources and Support Workplace Type This is a fully remote position. Application Deadline This position is anticipated to close on May 15, 2025. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email [email protected] for other accommodation options.