About the job Clinical Research Coordinator (Freshers) Location: RemoteOrganization: Clinogenesis Research OrganizationDepartment: Clinical OperationsEmployment Type: Full-Time Role Overview:The Clinical Research Associate (CRA) is the primary link between the sponsor and the clinical study sites. This role is responsible for monitoring clinical trials to ensure the safety of participants and the integrity of data. You will be tasked with ensuring site performance, protocol adherence, and regulatory compliance throughout the lifecycle of clinical studies. Key Responsibilities: Site Monitoring: Conduct Pre-study, Initiation, Routine Monitoring, and Close-out visits to ensure protocol compliance.Data Verification: Perform Source Data Verification (SDV) to ensure trial data is accurate, complete, and verifiable.Site Management: Provide guidance to study coordinators and investigators on study procedures and GCP requirements.Regulatory Oversight: Ensure that all Essential Documents are maintained in the Investigator Site File (ISF) and are audit-ready.Adverse Event Reporting: Ensure all Serious Adverse Events (SAEs) are reported within the mandated timelines.Subject Safety: Monitor patient recruitment and retention to ensure study milestones are met without compromising safety.Investigational Product (IP): Oversee the accountability, storage, and dispensing of investigational products at the site. Education Qualification: • B.Pharm / M.Pharm or Pharm.D. • B.Sc / M.Sc in Life Sciences (Biotechnology, Microbiology, Biochemistry). • BDS / BHMS / BAMS / MBBS. • Advanced Certification in Clinical Research/Clinical Data Management is highly preferred. Required Skills: • Solid understanding of ICH-GCP, local regulatory requirements (CDSCO), and clinical trial protocols. • Ability to travel frequently to various clinical trial sites. • Strong critical thinking and problem-solving skills for site-related issues. • Excellent interpersonal and communication skills to build professional relationships with investigators. • Proficiency in Clinical Trial Management Systems (CTMS) and EDC software. • High level of ethics and professional integrity. #clinicalresearchjobs #clinicalresearchassociate #CRA #clinicaltrials #hiring2026 #pharmajobs #lifesciencegraduates #clinicalresearch #clinicaloperations #hiring #jobopening #career #pharmacy #biotech #clinicalresearchcareer #clinogenesisresearchinstitute #fieldjobs #drugdevelopment #GCP #regulatorycompliance Earn certifications in these skills Learn VLSI Learn AI in Data Science Learn Clinical Trial Analysis & Reporting Salary Probation: Duration: Salary during probation: After probation: Annual CTC: Competitive salary Number of openings 1 Editor’s note Information above is Internshala's interpretation and paraphrasing of what we found on the shared link. Apply now Additional Questions × Close Sign up to continue Candidate sign up Sign up/ Login with Google Sign up with Email OR Email Password First Name Last Name Sign up By continuing as a candidate, you agree to our T&C. Already registered? Login var to_show_recaptcha = 0; Sign up to continue Candidate sign up Sign up/ Login with Google Sign up with Email OR Email Password First Name Last Name Sign up By continuing as a candidate, you agree to our T&C. Already registered? Login var to_show_recaptcha = 0; var to_trigger_already_applied_btn_ga = 0; Clinical Research Coordinator - Freshers Only ClinoGenesis Research Institute Chennai Start Date Starts Immediately CTC (ANNUAL) Competitive salary Competitive salary Experience No experience required No experience required Apply By Not Provided Posted few hours ago Fresher Job Be an early applicant Share on WhatsApp Share on LinkedIn Share on Facebook Share on Twitter Copy link Apply now Apply now About the job Clinical Research Coordinator (Freshers) Location: RemoteOrganization: Clinogenesis Research OrganizationDepartment: Clinical OperationsEmployment Type: Full-Time Role Overview:The Clinical Research Associate (CRA) is the primary link between the sponsor and the clinical study sites. This role is responsible for monitoring clinical trials to ensure the safety of participants and the integrity of data. You will be tasked with ensuring site performance, protocol adherence, and regulatory compliance throughout the lifecycle of clinical studies. Key Responsibilities: Site Monitoring: Conduct Pre-study, Initiation, Routine Monitoring, and Close-out visits to ensure protocol compliance.Data Verification: Perform Source Data Verification (SDV) to ensure trial data is accurate, complete, and verifiable.Site Management: Provide guidance to study coordinators and investigators on study procedures and GCP requirements.Regulatory Oversight: Ensure that all Essential Documents are maintained in the Investigator Site File (ISF) and are audit-ready.Adverse Event Reporting: Ensure all Serious Adverse Events (SAEs) are reported within the mandated timelines.Subject Safety: Monitor patient recruitment and retention to ensure study milestones are met without compromising safety.Investigational Product (IP): Oversee the accountability, storage, and dispensing of investigational products at the site. Education Qualification: • B.Pharm / M.Pharm or Pharm.D. • B.Sc / M.Sc in Life Sciences (Biotechnology, Microbiology, Biochemistry). • BDS / BHMS / BAMS / MBBS. • Advanced Certification in Clinical Research/Clinical Data Management is highly preferred. Required Skills: • Solid understanding of ICH-GCP, local regulatory requirements (CDSCO), and clinical trial protocols. • Ability to travel frequently to various clinical trial sites. • Strong critical thinking and problem-solving skills for site-related issues. • Excellent interpersonal and communication skills to build professional relationships with investigators. • Proficiency in Clinical Trial Management Systems (CTMS) and EDC software. • High level of ethics and professional integrity. #clinicalresearchjobs #clinicalresearchassociate #CRA #clinicaltrials #hiring2026 #pharmajobs #lifesciencegraduates #clinicalresearch #clinicaloperations #hiring #jobopening #career #pharmacy #biotech #clinicalresearchcareer #clinogenesisresearchinstitute #fieldjobs #drugdevelopment #GCP #regulatorycompliance Earn certifications in these skills Learn VLSI Learn AI in Data Science Learn Clinical Trial Analysis & Reporting Salary Probation: Duration: Salary during probation: After probation: Annual CTC: Competitive salary Number of openings 1 Editor’s note Information above is Internshala's interpretation and paraphrasing of what we found on the shared link. Apply now Additional Questions × Close Sign up to continue Candidate sign up Sign up/ Login with Google Sign up with Email OR Email Password First Name Last Name Sign up By continuing as a candidate, you agree to our T&C. Already registered? Login var to_show_recaptcha = 0; Sign up to continue Candidate sign up Sign up/ Login with Google Sign up with Email OR Email Password First Name Last Name Sign up By continuing as a candidate, you agree to our T&C. Already registered? Login var to_show_recaptcha = 0; var to_trigger_already_applied_btn_ga = 0; var is_post_auto_approved = 0; var is_internship_sent_for_followup_for_unpaid = ""; var is_internship_sent_for_followup_for_less_stipend = ""; var to_show_invite_applicant = true; var to_show_zapp_modal = false; var to_show_zapp_opt_in_modal = false; var internship_id = 3172031; var open_positions = 1;