Job Summary

InfoTech Solutions is seeking a detail-oriented and highly organized Clinical Research Associate (CRA) to support our remote Pharmaceutical Operations team. The successful candidate will be responsible for monitoring clinical trials, ensuring compliance with regulatory standards, maintaining data integrity, and collaborating with cross-functional teams to ensure the successful execution of clinical research studies. This is a remote role ideal for professionals with strong analytical skills and a passion for advancing healthcare innovation.

Key Responsibilities

Monitor clinical trial activities to ensure compliance with protocols, GCP (Good Clinical Practice), and regulatory requirements
Conduct remote site visits and evaluate study progress, data quality, and documentation accuracy
Collaborate with investigators, study coordinators, and project managers
Review and verify clinical data for completeness and consistency
Prepare and submit monitoring reports in a timely manner
Identify and escalate protocol deviations and compliance issues
Assist in the development and implementation of study documentation and SOPs
Ensure adherence to ethical standards and regulatory guidelines

Required Skills and Qualifications

Bachelor’s degree in Life Sciences, Pharmacy, Nursing, or related field
Strong understanding of clinical trial processes and regulatory frameworks
Excellent written and verbal communication skills
Strong attention to detail and organizational abilities
Proficiency in MS Office and clinical data management systems
Ability to work independently in a remote environment
Strong problem-solving and analytical thinking skills

Experience

2–5 years of experience in clinical research, clinical monitoring, or pharmaceutical operations preferred
Experience in remote or hybrid clinical trial environments is an advantage
Familiarity with ICH-GCP guidelines and FDA/EMA regulations

Working Hours

Full-time remote position
Standard working hours: Monday to Friday, flexible shifts based on project requirements
Occasional availability required for cross-time-zone collaboration

Knowledge, Skills and Abilities

Strong knowledge of clinical trial lifecycle and monitoring procedures
Ability to interpret clinical data and identify inconsistencies
High level of accuracy and documentation skills
Strong interpersonal skills to coordinate with global teams
Ability to manage multiple studies and deadlines simultaneously
Adaptability to evolving regulatory and project requirements

Benefits

Competitive salary package
Remote work flexibility
Health and wellness benefits
Paid time off and holidays
Professional development and training opportunities
Exposure to global clinical research projects
Career growth within the pharmaceutical operations domain

Why Join InfoTech Solutions

At InfoTech Solutions, we are committed to advancing healthcare through innovation and excellence in clinical research. Joining our team means becoming part of a collaborative, forward-thinking environment where your contributions directly impact global health outcomes. We value integrity, professional growth, and continuous learning.

How to Apply

Interested candidates are invited to submit their updated resume and a brief cover letter highlighting relevant experience to the InfoTech Solutions recruitment team. Shortlisted applicants will be contacted for the next stage of the selection process.

Clinical Research Associate – Remote Pharmaceutical Ops

Job Description