Assistant Clinical Research

Fortis; Gurugram District; On-site; INR 300,000 - 600,000; Full time

Job summary

Fortis Healthcare Ltd. in Gurugram seeks an Assistant Clinical Research professional to join our team. The role emphasizes supporting protocol development, study design, and regulatory compliance within clinical trials.

The candidate will collaborate with data management, biostatistics, medical writing, and site staff to ensure quality documentation and adherence to GCP, while maintaining rigorous study records.

Qualifications

• Bachelors in life sciences or related field.
• Strong understanding of GCP and regulatory requirements.
• Excellent analytical, problem-solving and communication skills.
• Ability to work in cross-functional teams and manage multiple projects.
• Familiarity with clinical trial databases and software is desirable.

Responsibilities

• Assist in developing and implementing clinical trial protocols and study designs.
• Coordinate with data management, biostatistics, and medical writing teams.
• Conduct literature reviews and analyze data to inform study design.
• Maintain accurate, up-to-date study documentation and progress records.
• Collaborate with investigators and site staff to ensure protocol compliance.
• Support quality control and quality assurance activities in trials.

Skills

Analytical skills

Problem solving

Communication skills

Team collaboration

Attention to detail

Organizational skills

Prioritization

Education

Bachelor's degree in life sciences

Tools

Trial management software

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.