Clinical Safety Project Assistant at Medpace, Inc.

Beijing, , China -

Full Time

Start Date

Immediate

Expiry Date

22 Aug, 26

Salary

0.0

Posted On

24 May, 26

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Clinical Safety, Organizational Skills, Prioritization, Microsoft Office, Attention To Detail, Oral Communication, Written Communication, Quality Control, Database Management, Report Preparation

Industry

Pharmaceutical Manufacturing

Description

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). We provide Phase I-IV 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 its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40+ countries. Why Medpace? People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today. The work we’ve done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future. Medpace Perks Flexible work environment Competitive compensation and benefits package Competitive PTO packages Structured career paths with opportunities for professional growth Company-sponsored employee appreciation events Employee health and wellness initiatives Awards Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024 Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility What to Expect Next A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.

Responsibilities

Provide administrative and operational support to the Clinical Safety department, including processing safety reports and tracking correspondence with regulatory authorities. Maintain databases, prepare meeting documentation, and perform quality control reviews of department documents.