Experienced Clinical Research Associate - (Home-based)

Medpace, Inc.; Malaysia; On-site; MYR 243,000 - 364,000; Full time

Benefits offered by this job

Competitive pay

Health & retirement benefits

WFH flexibility for eligible roles

Job summary

Medpace, Inc. in Malaysia is seeking a full-time, experienced Clinical Research Associate to join our Clinical Monitoring team.

You will conduct qualification, initiation, monitoring, and closeout visits in compliance with the protocol and regulatory requirements, supporting accurate data and patient safety. The role offers opportunities to collaborate with site staff, review regulatory documents, manage site qualifications, and contribute to ongoing trials across our global network.

Qualifications

• 1. 1.5 to 5 years of experience in clinical monitoring.
• 2. Willing to travel approximately 60-80% nationally.
• 3. Familiarity with Microsoft Office.
• 4. Strong communication and presentation skills.

Responsibilities

• Conduct qualification, initiation, monitoring, and closeout visits for research sites in compliance with the protocol.
• Communicate with site staff including coordinators, investigators, and staff.
• Verify investigator qualifications, training, resources, facilities, laboratories, equipment, and staff.
• Verify case report form data and inform site staff of errors, ensuring good documentation practices and regulatory compliance.
• Ensure investigator enrollment of eligible subjects and review regulatory documents.
• Manage medical device/investigational product accountability and inventory.
• Review adverse events and concomitant medications for accurate data reporting.
• Assess patient recruitment/retention at sites and suggest improvements.
• Prepare monitoring reports and follow-up letters with summaries of findings and corrective actions.

Skills

Clinical monitoring experience

Travel readiness

Strong communication

Microsoft Office

Education

Bachelor’s degree in Health or Life Science

Tools

Microsoft Office

Job description

Job Summary

We are currently seeking a full-time, experienced Clinical Research Associate to join our Clinical Monitoring team in the Malaysia. 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 and develop and grow your career even further, then this is the opportunity for you.

Our culture is of expertise, and we empower our teams to employ their unique talents and experience to take an assertive approach to research, problem solving, and ultimately supporting our business partners. At Medpace, our employees embody our values and our approach to serving our clients. They work hard, understand our high expectations, and rise to the challenge. In return they are rewarded with interesting projects, career advancement, and recognition and exposure to our international footprint. These are just a few reasons why talented individuals join the Medpace team.

Through our PACE® Training Program, you will join other ProfessionalsAchieving CRA Excellence and receive customized, expedited training, and efficient onboarding to familiarize experienced CRAs with Medpace systems.

Responsibilities

• Conduct qualification, initiation, monitoring, and closeout visits for research sites in compliance with the approved protocol;
• Communication with the medical site staff including coordinators, clinical research physicians and their site staff;
• Verifying adequate investigator qualifications, training and resources, including facilities, laboratories, equipment, and staff;
• Medical record and research source documentation verification against case report form data, including informing the site staff of any entry errors, ensuring good documentation practices are being adhered to and communicating protocol deviations appropriately per SOPs, GCP and applicable regulatory requirements;
• Verification that the investigator is enrolling only eligible subjects;
• Regulatory document review;
• Medical device and/or investigational product/drug accountability and inventory;
• Verification and review of adverse events, serious adverse events, concomitant medications and corresponding illnesses to confirm accurate data reporting in accordance with the protocol;
• Assessing the clinical research site’s patient recruitment and retention success and offering suggestions for improvement;
• Completion of monitoring reports and follow-up letters, which includes providing summaries of the significant findings, deviations, deficiencies, and recommended actions to secure compliance.

Qualifications

• Bachelor’s degree in Health or Life Science related field preferred;
• At least 1.5 to 5 years of experience in clinical monitoring;
• Willing to travel approximately 60-80% nationally;
• Familiarity with Microsoft® Office; and
• Strong communication and presentation skills a plus.

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.