Randomization & Study Product Coordinator

Our corporate activities are growing rapidly, and we are currently seeking a full-time, office-based RSP (Randomization & Study Product) Coordinator to join our team in India. By working with the other RSPM team members, these professionals ensure the accuracy of RSPM system data, as well as assisting in the management of study product for studies. If you are detail-oriented and enjoy an adaptive, challenging work environment, this could be the opportunity for you. This is an entry level role. As new hires, RSPM Coordinators go through an extensive onboarding and training process, which prepares them to become experts in their field. Responsibilities - General Randomization & Study Product Management support; - Study product management; - Assist the Project Manager in system design and set-up; - Work with clients in obtaining requirements and responding to inquiries; - Create study specific documents; - Maintain study documentation; and - Other assigned projects and tasks. Qualifications - Bachelor's degree (required) in a life science or related field; - Basic knowledge of clinical research methodologies - Advance working knowledge of Excel; - Strong attention to detail   Medpace Overview Medpace is a full-service clinical contract research organization (CRO) providing phase l-lV clinical development services to the biotechnology, pharmaceutical, and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through the advancement of clinical research. We leverage in-country regulatory and therapeutic expertise across all major therapeutic areas including oncology, cardiology, metabolic, endocrinology, central nervous system, and anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, we employ more than 6,500 people across 40+ countries. Why Medpace? When you join Medpace, you become part of an innovative team that brings cutting-edge therapies to market while building a meaningful and rewarding career focused on scientific excellence and improving patient outcomes around the world through continuous learning and cross-functional collaboration.   Purpose-Driven Work - - Work alongside physicians, scientists, and industry-leading experts committed to advancing the global development of medical therapeutics through clinical research excellence   Collaborative Culture - - Contribute to an interactive team environment that empowers decision making, creative thinking, and continuous learning through open communication and mutual trust. - Leadership throughout Medpace is both accessible and approachable   Continuous Growth & Development - - Office based environment with on-site mentors - Defined career paths with clear advancement opportunities - Industry renowned onboarding and training programs designed to accelerate professional development - Ongoing training and continuous learning opportunities throughout your career - An environment that encourages employees to influence change, contribute ideas, and grow quickly   Other Employee Benefits - - Competitive compensation programs that recognize and reward performance - Comprehensive health, wellness, retirement, and PTO benefits - Office based culture with occasional WFH that provides flexibility for eligible positions after training - Company-sponsored social events    Please note benefits may vary based on country.      What to Expect Next A Medpace team member will review your application and if your profile matches our current needs, you will be contacted for an interview. While we review all applications carefully, we are unable to respond to every applicant, and only candidates selected for interviews will be contacted. - General Randomization & Study Product Management support; - Study product management; - Assist the Project Manager in system design and set-up; - Work with clients in obtaining requirements and responding to inquiries; - Create study specific documents; - Maintain study documentation; and - Other assigned projects and tasks. - Bachelor's degree (required) in a life science or related field; - Basic knowledge of clinical research methodologies - Advance working knowledge of Excel; - Strong attention to detail