Description

Senior clinical research associates (CRAs) handle the day-to-day operations of the clinical investigative phase of drug development. They are in charge of laboratory and research duties to reach all the organizational objectives. They need to have strong analytical aptitudes and pay strict attention to detail during all clinical research. They also handle experiment inquiries and take assessment notes on a frequent basis. Most senior clinical research associates are in charge of keeping investigative reports and providing project communications.

Frequently, senior clinical research associates work in a lab setting, and their schedule can vary according to their projects and company needs.. They are responsible for monitoring experiment tools in this laboratory setting and any variables that may impact the research. They also must effectively train other research associates to operate complex equipment and follow proper laboratory conduct. They also work with different research professionals to share research results and reach different conclusions.

A bachelor's degree in a scientific discipline, at minimum, is required for this position, as well as years of successful laboratory experience and additional certifications and/or education. These research associates need to have excellent interpersonal skills to cooperate in a team environment and deliver conclusions to research managers. They are also required to uphold ethical research practices and maintain advanced safety standards.

Roles & Responsibilities

As a Senior Clinical Research Associate CRA with 3-6 years of experience in Singapore, your main responsibilities include:

  • Oversee clinical trials, ensuring compliance with protocols, standard operating procedures, and regulatory requirements, while maintaining accurate and complete documentation.
  • Conduct site initiation, monitoring, and closeout visits, perform source data verification, and ensure site compliance and patient safety throughout the trial.
  • Collaborate with investigators, study coordinators, and cross-functional teams to ensure timely enrollment, accurate data collection, and resolution of study-related issues.
  • Mentor and train junior CRAs, provide guidance on study protocols, regulatory guidelines, and best practices, and assist with study-specific trainings and audits.

Qualifications & Work Experience

For a Senior Clinical Research Associate (CRA) job role, the following qualifications are required:

  • The candidate should have a strong background in clinical research and a deep understanding of Good Clinical Practice (GCP) guidelines. They should have worked on multiple clinical trials, demonstrating their knowledge of study protocols, data collection, and management.
  • A Senior CRA should be able to identify and address issues that arise during clinical trials effectively. They should have the ability to analyze complex clinical data, identify trends, and propose appropriate solutions to ensure the integrity of the study.
  • It is crucial for a Senior CRA to have exceptional communication skills to effectively communicate with study investigators, site personnel, and sponsor representatives. They should be able to build strong relationships and effectively collaborate with cross-functional teams.
  • As a Senior CRA, attention to detail is essential to ensure data accuracy and project timelines are met.

Essential Skills For Senior Clinical Research Associate (CRA)

1

Clinical Research

2

Research and Analysis

3

Project Management

4

Research Methods

Career Prospects

The role of a Senior Clinical Research Associate CRA in Singapore, with 3-6 years of experience, is crucial in the field of clinical research. For professionals looking for alternative career avenues, here are following options to consider:

  • Clinical Project Manager: This role involves overseeing multiple clinical trials, managing project timelines, budgets, and ensuring compliance.
  • Regulatory Affairs Specialist: A position focused on navigating the complex regulatory landscape, ensuring adherence to guidelines and obtaining necessary approvals.
  • Clinical Data Manager: This role involves managing and optimizing clinical trial data, ensuring its accuracy, integrity, and regulatory compliance.
  • Pharmacovigilance Specialist: A position focused on monitoring and evaluating the safety and effectiveness of medications, ensuring compliance with reporting requirements.

How to Learn

The role of Senior Clinical Research Associate (CRA) in Singapore shows promising growth in the market. Over the past 10 years, the job role has experienced steady expansion, with a positive trend projected for the future. According to recent data, the demand for Senior CRAs is expected to increase in the coming years due to the growing pharmaceutical and healthcare industries in Singapore. This growth is anticipated to bring about a significant number of employment opportunities for individuals aspiring to work as Senior CRAs in Singapore.