Clinical Safety Project Assistant

Our corporate activities are growing rapidly, and we are currently seeking a full-time, office-based Project Assistant to join our Clinical Safety team. This position will work on a team to accomplish tasks and projects that are instrumental to the company’s success. If you want an exciting career where you use your previous expertise and can develop and grow your career even further, then this is the opportunity for you.

Responsibilities

• Perform a variety of support tasks to the Clinical Safety department, which may include bu not limited to processing safety reports, creating and distributing safety notification letters, tracking and filling of all corresponsence with Regulatory Authorities, Local Ethics Committees, Sites and/or GCP offices; • Prepare reports, presentations, agendas, correspondence, and meeting minutes as necessary; • Track, process, and organize various safety-related documents; • May perform basic research, answer questions from internal or external parties, or identify potential issues for further investigation in support of Clinical Safety department processes; • Develop understanding and perform tasks in accordance with assigned SOPs and policies; • Conduct quality control reviews of department documents, as necessary; • Maintain database/spreadsheets, as needed, to facilitate tracking/documentation of department activities; • May mentor and train less experienced project assistants; • Perform other duties as assigned by the Clinical Safety department.

Qualifications

• A minimum of an Associate degree or equivalent; • At least 1 year of clinical safety experience is necessary; • Excellent organizational and prioritization skills are needed; • Knowledge of Microsoft Office required; and • Applicants should have great attention to detail and excellent oral and written communication skills.

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.