Clinical Safety Coordinator - Pharmacovigilance / Drug Safety

Medpace; Singapore; On-site; USD 50,000 - 90,000; Full time

Job summary

Join a forward-thinking clinical research organization as a Clinical Safety Coordinator in Singapore. This exciting full-time role is essential for ensuring the safety of clinical trials and involves collaborating closely with the Clinical Safety Manager. You will collect and track adverse event reports, generate safety narratives, and assist in preparing clinical safety documents. With a commitment to improving patient lives, this organization offers a supportive environment for professional growth and development. If you're passionate about making a difference in the medical field, this opportunity is for you!

Benefits

Flexible work environment

Competitive compensation and benefits package

Competitive PTO packages

Structured career paths

Company-sponsored employee appreciation events

Employee health and wellness initiatives

Qualifications

• 1 year of clinical safety experience or 2 years in pharmaceutical research.
• Proficient in Clinical Safety tasks and Good Clinical Practice (GCP) guidelines.

Responsibilities

• Collaborate with the Clinical Safety Manager to meet project deliverables.
• Collect and process serious adverse event (SAE) reports.

Skills

Clinical Safety Expertise

Time Management

Team Collaboration

Attention to Detail

Education

Bachelor’s degree in health/life sciences

Tools

Microsoft Office

Safety Database

Job description

Job Summary

We are currently seeking a full-time, office-based Clinical Safety Coordinator to join our team in Singapore office. This role is a vital part of the team to accomplish tasks and projects that are instrumental to the company’s success. If you are interested in an exciting career where you can use your expertise, develop and grow your career even further, then this is the opportunity for you.

Responsibilities

1. Working closely with the Clinical Safety Manager to ensure each project deliverables are met;
2. Collect, process, and track serious adverse event (SAE) reports and clinical event documents;
3. Generate and track study report safety narratives;
4. Coordinate safety surveillance activities (e.g., lab review and trend analysis);
5. Generate Investigator Safety Letters and distribution to health authority;
6. Assist in preparation of clinical safety documents;
7. Perform safety submissions of expedited/periodic reports in Singapore/Taiwan/China.

Qualifications

1. Bachelor’s degree in health/life sciences with 1 year of clinical safety experience or 2 years of pharmaceutical research experience;
2. Proficient in a range of Clinical Safety tasks, as detailed in the ‘responsibilities’ section (above);
3. Excellent time management skills with an ability to work on tight timelines;
4. An ability to interact well within a team environment, but also work independently and manage own workload;
5. Proficient in Microsoft Office and demonstrated ability to efficiently use safety database;
6. Strong attention to detail;
7. Demonstrate comprehensive knowledge of Good Clinical Practice (GCP) guidelines.

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.

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