Study Coordination: Assist in the design and development of study protocols and case report forms (CRFs) Coordinate the logistics of clinical trials or medical research projects Manage timelines, budgets, and resources for research studies Site & Data Management: Support site selection and initiation Monitor clinical trial sites to ensure compliance with protocols and regulations Collect, review, and verify study data for accuracy and completeness Maintain regulatory documentation and study master files Regulatory & Ethical Compliance: Ensure adherence to Good Clinical Practice (GCP), ICH guidelines, and applicable laws (e.g., CDSCO in India, FDA in the US) Assist in ethics committee/institutional review board (IRB) submissions and communications Support preparation of study reports and submissions to regulatory authorities Job Type: Full-time Pay: From ₹10,000.00 per month Schedule: Day shift Supplemental Pay: Performance bonus Work Location: In person
Study Coordination: Assist in the design and development of study protocols and case report forms (CRFs) Coordinate the logistics of clinical trials or medical research projects Manage timelines, budgets, and resources for research studies Site & Data Management: Support site selection and initiation Monitor clinical trial sites to ensure compliance with protocols and regulations Collect, review, and verify study data for accuracy and completeness Maintain regulatory documentation and study master files Regulatory & Ethical Compliance: Ensure adherence to Good Clinical Practice (GCP), ICH guidelines, and applicable laws (e.g., CDSCO in India, FDA in the US) Assist in ethics committee/institutional review board (IRB) submissions and communications Support preparation of study reports and submissions to regulatory authorities Job Type: Full-time Pay: From ₹10,000.00 per month Schedule: Day shift Supplemental Pay: Performance bonus Work Location: In person
Job Description – Clinical Research Executive (Entry Level) Position Overview The Clinical Research Executive will be responsible for coordinating, monitoring, and managing clinical research studies in compliance with ICH-GCP, regulatory guidelines, and company SOPs. The role involves supporting protocol development, site management, documentation, and regulatory submissions for clinical trials of drugs, biologics, nutraceuticals, or cosmetics. Key Responsibilities Assist in the design, development, and review of clinical trial protocols, case report forms (CRFs), informed consent forms (ICFs), and study-related documents. Coordinate with Ethics Committees, regulatory authorities (e.g., CDSCO, IECs), and external stakeholders for submissions, approvals, and reporting. Support site identification, feasibility studies, and investigator selection. Oversee initiation, monitoring, and close-out visits at study sites to ensure compliance with GCP and study protocol. Track patient recruitment, enrollment, and data collection activities. Maintain trial master files and essential study documentation. Coordinate with CROs, labs, and vendors for study-related activities. Assist in pharmacovigilance reporting, safety updates, and adverse event documentation. Prepare and review clinical study reports, interim reports, and regulatory documents. Ensure adherence to SOPs, ICH-GCP, regulatory requirements, and company policies. Qualifications & Skills Bachelor’s or Master’s degree in Life Sciences, Pharmacy, Biotechnology, or related field. Good knowledge of ICH-GCP, NDCT Rules (India), and regulatory requirements. Strong documentation, and multitasking skills. Excellent written and verbal communication skills. Proficiency in MS Office (Word, Excel, PowerPoint). Preferred Attributes This job is for Entry level freshers Local candidates are preferred (Near by office address). Knowledge of pharmacovigilance, BA/BE studies, or medical writing is an advantage. Ability to work independently as well as in a team environment. Job Type: Full-time Pay: ₹10,000.00 - ₹15,000.00 per month Benefits: Food provided Paid sick time Work Location: In person
Job Description – Clinical Research Executive (Entry Level) Position Overview The Clinical Research Executive will be responsible for coordinating, monitoring, and managing clinical research studies in compliance with ICH-GCP, regulatory guidelines, and company SOPs. The role involves supporting protocol development, site management, documentation, and regulatory submissions for clinical trials of drugs, biologics, nutraceuticals, or cosmetics. Key Responsibilities Assist in the design, development, and review of clinical trial protocols, case report forms (CRFs), informed consent forms (ICFs), and study-related documents. Coordinate with Ethics Committees, regulatory authorities (e.g., CDSCO, IECs), and external stakeholders for submissions, approvals, and reporting. Support site identification, feasibility studies, and investigator selection. Oversee initiation, monitoring, and close-out visits at study sites to ensure compliance with GCP and study protocol. Track patient recruitment, enrollment, and data collection activities. Maintain trial master files and essential study documentation. Coordinate with CROs, labs, and vendors for study-related activities. Assist in pharmacovigilance reporting, safety updates, and adverse event documentation. Prepare and review clinical study reports, interim reports, and regulatory documents. Ensure adherence to SOPs, ICH-GCP, regulatory requirements, and company policies. Qualifications & Skills Bachelor’s or Master’s degree in Life Sciences, Pharmacy, Biotechnology, or related field. Good knowledge of ICH-GCP, NDCT Rules (India), and regulatory requirements. Strong documentation, and multitasking skills. Excellent written and verbal communication skills. Proficiency in MS Office (Word, Excel, PowerPoint). Preferred Attributes This job is for Entry level freshers Local candidates are preferred (Near by office address). Knowledge of pharmacovigilance, BA/BE studies, or medical writing is an advantage. Ability to work independently as well as in a team environment. Job Type: Full-time Pay: ₹10,000.00 - ₹15,000.00 per month Benefits: Food provided Paid sick time Work Location: In person