Clinical Research Associate

Proxima Skills Academy; Kolkata District; On-site; INR 500,000 - 900,000; Full time

Job summary

Proxima Skills Academy in Kolkata seeks a Clinical Research Associate for a full-time, on-site role. You will support planning, implementation, and monitoring of clinical trials, coordinating with sites and investigators to ensure data integrity and regulatory compliance.

The role involves reviewing forms, assisting in site training, and maintaining ethical SOP-driven processes to promote high-quality research outcomes and learner mentoring where relevant.

Qualifications

• Degree in Life Sciences, Pharmacy, Nursing, Biotechnology or related field.
• Knowledge of GCP and regulatory standards.
• Experience or understanding of Clinical Trials and study phases.
• Strong attention to detail and organizational skills.
• Effective written and verbal communication, collaborative work.

Responsibilities

• Coordinate with clinical sites to support trial activities.
• Assist in study start-up activities and regulatory compliance.
• Ensure accurate data collection and documentation across trials.
• Review case report forms and support site training on SOPs.
• Track study progress and communicate with investigators and stakeholders.

Skills

Protocol development

Site communication

Monitoring support

Documentation management

Data review

Literature search

Report preparation

Clinical operations

Study coordination

SOP-driven processes

GCP knowledge

Multitasking

Education

Life Sciences/Pharmacy/Nursing/Biotechnology related degree

Job description

Role Description The Clinical Research Associate role is a full-time, on-site position based in Kolkata. The individual in this role will support the planning, implementation, and monitoring of clinical trials in line with approved protocols and regulatory requirements. Day-to-day responsibilities include coordinating with clinical sites, assisting in study start-up activities, ensuring accurate data collection and documentation, and tracking study progress. The role involves reviewing case report forms, supporting site training on study procedures, and helping maintain compliance with ethical guidelines and standard operating procedures. The Clinical Research Associate will collaborate with clinical operations teams, investigators, and other stakeholders to promote high-quality research outcomes and contribute to learner training and mentoring where relevant.

Qualifications

• Candidates should possess strong knowledge of clinical trial Protocol development, interpretation, and adherence.
• Candidates should possess skills related to the Clinical Research Associate function, including site communication, monitoring support, and documentation management.
• Candidates should possess experience or understanding of Clinical Trials, including study phases, regulatory requirements, and ethical guidelines.
• Candidates should possess solid Research skills, such as data review, analysis basics, literature search, and report preparation.
• Candidates should possess familiarity with Clinical Operations, including study coordination, site management, and SOP-driven processes.
• Relevant degree in Life Sciences, Pharmacy, Nursing, Biotechnology, or a related field.
• Knowledge of Good Clinical Practice (GCP) and applicable regulatory standards.
• Strong attention to detail, organizational skills, and the ability to manage multiple tasks and timelines.
• Effective written and verbal communication skills and ability to work collaboratively with multidisciplinary teams.
• Prior internship or experience in clinical research or healthcare settings is an advantage.