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 6-9 years of experience in Singapore, your main responsibilities include:

  • Conducting site initiation, monitoring, and close-out visits for clinical trials, ensuring compliance with protocols, regulations, and Good Clinical Practice GCP guidelines.
  • Overseeing site selection and qualification processes, including assessing potential investigational sites and establishing strong relationships with site staff.
  • Providing ongoing training and support to site staff, ensuring proper implementation of study protocols and accurate data collection.
  • Reviewing and analyzing clinical trial data, preparing reports and documentation, and ensuring data integrity and accuracy throughout the trial process.

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)

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Clinical Research

Skills That Affect Senior Clinical Research Associate (CRA) Salaries

Different skills can affect your salary. Below are the most popular skills and their effect on salary.

Clinical Research

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Career Prospects

The role of a Senior Clinical Research Associate CRA is crucial in the field of clinical research. With 6-9 years of experience in Singapore, professionals in this role may consider exploring alternative career opportunities. Here are following alternative roles to consider:

  • Clinical Research Project Manager: A position that involves overseeing and managing clinical research projects, including protocol development, team coordination, and resource allocation.
  • Clinical Trial Manager: A role focused on planning, executing, and monitoring clinical trials, ensuring compliance with regulations and protocols.
  • Quality Assurance Specialist: A position that involves ensuring compliance with quality standards and regulatory requirements in clinical research, including implementing and maintaining quality management systems.
  • Medical Affairs Manager: A role that involves collaborating with cross-functional teams to provide medical and scientific support for clinical research activities, including developing scientific communications and managing relationships with key stakeholders.

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.