Clinical Research Associate
Role Overview
As a Clinical Research Associate trainee, you will undergo intensive training to master clinical trial operations, documentation, and regulatory compliance. You'll assist with managing Trial Master Files, site files, and Case Report Forms while supporting senior mentors in daily clinical activities and patient coordination. This entry-level role is designed for recent graduates to gain practical industry skills.
Perks & Benefits
This is a fully remote training program with mentorship from industry experts, providing hands-on exposure to global clinical trial standards. You'll have a clear growth path within a globally recognized organization, ideal for building a long-term career in clinical research.
Full Job Description
Clinical Research Associate (Trainee/Freshers Only)Organization: Clinogenesis Research OrganizationLocation: Remote (India)Department: Clinical OperationsEmployment Type: Full-TimeAbout the RoleAre you a recent graduate eager to start a career in Clinical Research but finding it difficult to gain entry? Clinogenesis Research Organization is bridging the gap between graduation and professional success. We are offering an exclusive, entry-level Career Launchpad designed specifically for freshers.This is not just a job; it is a dedicated training program where we teach you the actual industry-required skills necessary to excel as a Clinical Research Associate (CRA). We transform your academic knowledge into practical, real-world expertise.Why Join Our Program?Skill-First Training: We bridge the gap between your degree and the job market by providing intensive training on industry-standard operations.Mentorship: Work directly with industry experts who are committed to your professional development.Hands-on Exposure: Gain practical experience in global clinical trial standards, moving beyond textbook theory.Clear Growth Path: A structured roadmap within a globally recognized organization designed to evolve you into a seasoned professional.Key ResponsibilitiesIndustry Skill Mastery: Actively participate in specialized training sessions to master clinical operations, documentation, and regulatory compliance.Site & Documentation Support: Learn to manage Trial Master Files (TMF), site files, and Case Report Forms (CRF) with accuracy.Protocol Compliance: Gain a deep understanding of ICH-GCP, ethical guidelines, and local regulatory requirements.Operational Assistance: Assist in the daily management of clinical trial activities and patient coordination under the guidance of senior mentors.Eligibility Criteria (Strictly Freshers)Education: B.Pharma, M.Pharma, D.Pharma, and all Life Sciences graduates (B.Sc/M.Sc in Biotechnology, Microbiology, Nursing, Biochemistry, or equivalent healthcare fields).Batch: 2024, 2025, and 2026 graduates (Final year students are highly encouraged to apply).Experience: Strictly 0 years. We are looking for fresh talent ready to be molded. Candidates with prior professional clinical research experience will not be considered.Skills: Exceptional communication, a high level of organization, and a genuine passion for building a long-term career in the life sciences industry.How to ApplyIf you are ready to transition from a student to a professional, we want to hear from you! Join our Fresher Intake Program and let us help you launch your clinical research career.#ClinicalResearch #CRA #FreshersHiring #PharmaJobs #LifeSciences #DPharma #BPharma #MPharma #CareerLaunchpad #JobSearch2026 #ClinicalTrials #EntryLevelJobs #HiringFreshers #clinicalresearchassociatePlease mention the word **POIGNANT** and tag RMmEwMTo0Zjk6YzAxMzo3ZjU5Ojox when applying to show you read the job post completely (#RMmEwMTo0Zjk6YzAxMzo3ZjU5Ojox). This is a beta feature to avoid spam applicants. Companies can search these words to find applicants that read this and see they're human.