Job Summary

InfoTech Solutions is seeking a detail-oriented and highly motivated Clinical Research Associate (CRA) to support remote pharmaceutical operations. The ideal candidate will play a critical role in ensuring clinical trials are conducted in compliance with regulatory requirements, company SOPs, and Good Clinical Practice (GCP) standards. This position involves close collaboration with cross-functional teams, investigative sites, and sponsors to ensure high-quality data and successful study execution. The role is fully remote and suited for professionals who thrive in a fast-paced, quality-driven research environment.

Key Responsibilities

• Monitor clinical trial sites remotely and/or on-site to ensure protocol compliance and data integrity.

• Review and verify clinical data, source documentation, and regulatory files.

• Ensure adherence to ICH-GCP guidelines, SOPs, and applicable regulatory requirements.

• Support site selection, initiation, monitoring visits, and close-out activities.

• Identify and escalate risks, protocol deviations, and compliance issues in a timely manner.

• Maintain accurate and up-to-date trial master file (TMF) documentation.

• Collaborate with clinical project managers, data management, and regulatory teams.

• Provide training and guidance to investigative site staff when required.

• Prepare monitoring reports and follow-up letters within established timelines.

Required Skills and Qualifications

• Bachelor’s degree in Life Sciences, Pharmacy, Nursing, or a related field.

• Strong understanding of clinical trial processes and regulatory requirements.

• Proficiency in electronic data capture (EDC) systems and clinical trial management systems (CTMS).

• Excellent attention to detail and organizational skills.

• Strong written and verbal communication abilities.

• Ability to work independently in a remote environment.

• Proficient in Microsoft Office Suite and clinical documentation tools.

Experience

• Minimum 2–5 years of experience as a Clinical Research Associate or in clinical monitoring.

• Experience in pharmaceutical, biotech, or CRO environments preferred.

• Prior exposure to remote monitoring and decentralized trials is an advantage.

• Experience across multiple therapeutic areas is desirable.

Working Hours

• Full-time remote position.

• Flexible scheduling with availability to align with global study teams.

• Occasional travel may be required based on study needs.

Knowledge, Skills, and Abilities

• In-depth knowledge of ICH-GCP, FDA, and international regulatory requirements.

• Strong risk assessment and problem-solving capabilities.

• Ability to manage multiple studies and priorities simultaneously.

• High level of professionalism and ethical judgment.

• Strong interpersonal skills with the ability to build site relationships remotely.

• Adaptability in a technology-driven clinical environment.

Benefits

• Competitive salary and performance-based incentives.

• Comprehensive health and wellness benefits.

• Remote work flexibility.

• Professional development and certification support.

• Paid time off and company holidays.

• Opportunity to work on innovative clinical programs.

Why Join

At InfoTech Solutions, you will be part of a forward-thinking team committed to advancing pharmaceutical innovation through high-quality clinical research. The organization fosters a collaborative remote culture, invests in employee growth, and provides opportunities to work on impactful global studies. This is an excellent opportunity for professionals who want to contribute to meaningful healthcare advancements while enjoying flexible work arrangements.

How to Apply

Qualified candidates are encouraged to submit their updated resume along with a brief cover letter highlighting relevant clinical monitoring experience. Applications will be reviewed on a rolling basis, and shortlisted candidates will be contacted for the next steps in the selection process.