Assistant Clinical Research

Fortis; Chennai District; On-site; INR 300,000 - 450,000; Full time

Job summary

Fortis Healthcare Ltd. seeks an enthusiastic Assistant Clinical Research professional to support protocol development, study design, data management and regulatory compliance. You will collaborate with cross-functional teams to ensure efficient trial execution and high-quality documentation.

You will conduct literature reviews, analyze data, maintain trial records and assist investigators to uphold GCP standards and regulatory requirements across trials.

Qualifications

• Bachelor's degree in life sciences or related field.
• Strong understanding of GCP guidelines and regulatory requirements.
• Excellent analytical, problem-solving and communication skills.
• Ability to work effectively in a team and collaborate across disciplines.
• Strong attention to detail and ability to manage multiple projects.

Responsibilities

• Assist in development and implementation of clinical trial protocols and study designs.
• Coordinate with cross-functional teams including data management, biostatistics and medical writing.
• Conduct literature reviews and analyze data to inform study design decisions.
• Develop and maintain accurate study documentation and progress records.
• Collaborate with investigators and site staff to ensure protocol compliance.
• Provide support for quality control and quality assurance activities in trials.

Skills

Analytical skills

Problem-solving

Communication skills

Education

Bachelor's degree in life sciences

Tools

Clinical trial databases

Job description

We are looking for a highly motivated and detail-oriented individual to join our team as an Assistant Clinical Research professional at Fortis Healthcare Ltd. The ideal candidate will have a strong foundation in clinical research principles and practices, with excellent analytical and problem-solving skills.

Roles and Responsibility

• Assist in the development and implementation of clinical trial protocols and study designs.
• Coordinate with cross-functional teams, including data management, biostatistics, and medical writing.
• Conduct literature reviews and analyze data to inform study design and methodology decisions.
• Develop and maintain accurate and up-to-date records of study documentation and progress.
• Collaborate with investigators and site staff to ensure compliance with study protocols and regulations.
• Provide support for quality control and quality assurance activities related to clinical trials.

Job Requirements

• Bachelor's degree in a life science discipline or a related field.
• Strong understanding of clinical research principles, including GCP guidelines and regulatory requirements.
• Excellent analytical, problem-solving, and communication skills.
• Ability to work effectively in a team environment and collaborate with colleagues across disciplines.
• Strong attention to detail and organizational skills, with the ability to prioritize tasks and manage multiple projects simultaneously.
• Familiarity with clinical trial databases and software applications is desirable.