Job Summary

InfoTech Solutions is seeking a highly motivated and detail-oriented Clinical Research Associate (CRA) to join our Remote Pharmaceutical Operations team. In this role, you will be responsible for overseeing and monitoring clinical trials to ensure compliance with regulatory requirements, study protocols, and Good Clinical Practice (GCP) guidelines.

As a Clinical Research Associate, you will collaborate with investigators, site staff, and cross-functional teams to support the successful execution of clinical studies. This position offers the opportunity to work remotely while contributing to innovative pharmaceutical research that improves patient outcomes and advances medical science.

Key Responsibilities

• Monitor and manage assigned clinical trial sites to ensure adherence to study protocols, regulatory requirements, and GCP standards.

• Conduct remote and occasional on-site monitoring visits including site initiation, routine monitoring, and close-out visits.

• Review clinical trial data for accuracy, completeness, and consistency.

• Ensure timely and accurate documentation of trial-related activities, including monitoring reports and follow-up letters.

• Support site staff with protocol training and guidance throughout the study lifecycle.

• Identify potential risks, protocol deviations, and compliance issues, and implement corrective actions when necessary.

• Maintain effective communication with investigators, study coordinators, sponsors, and internal teams.

• Assist with regulatory submissions, ethics committee documentation, and clinical trial master file (TMF) maintenance.

• Ensure patient safety and data integrity across all study activities.

Required Skills and Qualifications

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

• Strong understanding of clinical research processes, GCP guidelines, and regulatory requirements.

• Excellent analytical and problem-solving skills.

• Strong written and verbal communication abilities.

• Ability to manage multiple studies and deadlines simultaneously.

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

• Strong organizational skills with high attention to detail.

• Ability to work independently in a remote work environment.

Experience

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

• Experience monitoring pharmaceutical or biotechnology clinical trials.

• Prior experience working with CROs, pharmaceutical companies, or research institutions is highly desirable.

• Experience in remote monitoring and decentralized clinical trials is an advantage.

Working Hours

• Full-time position.

• Standard working schedule of 40 hours per week.

• Flexible working hours with occasional coordination across global time zones.

• Some travel may be required for site visits or investigator meetings when necessary.

Knowledge, Skills, and Abilities

• In-depth knowledge of ICH-GCP guidelines and regulatory compliance.

• Ability to interpret clinical protocols and regulatory documents.

• Strong data review and risk assessment capabilities.

• Ability to maintain confidentiality and handle sensitive research data.

• Excellent teamwork and collaboration skills across cross-functional teams.

• Strong adaptability in a fast-paced research environment.

Benefits

• Competitive salary package.

• Remote work flexibility.

• Health and wellness benefits.

• Professional development and certification support.

• Paid time off and company holidays.

• Opportunities to participate in innovative global clinical trials.

• Career growth within a rapidly expanding healthcare technology organization.

Why Join InfoTech Solutions

At InfoTech Solutions, we are committed to advancing healthcare innovation through cutting-edge research and technology. Our team works collaboratively across global markets to support pharmaceutical advancements that improve lives worldwide. By joining our organization, you will gain the opportunity to contribute to meaningful clinical research projects, expand your professional expertise, and work in a flexible remote environment that values innovation, integrity, and excellence.

How to Apply

Interested candidates are invited to submit their updated resume and a brief cover letter outlining their clinical research experience and interest in the role.

Applications can be submitted through the InfoTech Solutions careers portal or via the official recruitment email listed on our website. Shortlisted candidates will be contacted for further evaluation, which may include virtual interviews and technical discussions with the clinical operations team.