Project Assistant- Clinical Safety at Medpace, Inc.

, , Singapore -

Full Time

Start Date

Immediate

Expiry Date

11 Mar, 26

Salary

0.0

Posted On

11 Dec, 25

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Organizational Skills, Prioritization Skills, Attention to Detail, Oral Communication, Written Communication, Administrative Experience, Knowledge of Word, Knowledge of Excel, Knowledge of PowerPoint

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 supporting tasks to the Clinical Safety department, which may include but not limited to processing safety reports, and tracking and filing of all correspondence with Regulatory Authorities and Sites; 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 required; 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 Bachelor degree in health/life sciences; Administrative experience in healthcare is a plus; Excellent organizational and prioritization skills are needed; Knowledge of Word, Excel, and PowerPoint is 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 6,000 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

The Project Assistant will perform a variety of supporting tasks for the Clinical Safety department, including processing safety reports and organizing safety-related documents. Additional responsibilities include preparing reports and conducting quality control reviews of department documents.