1,444 Clinical Research Associate jobs in India

Job Opening: Clinical Research Coordinator (Fresher)

 Location: (Insert Location)

Organization: ClinoGenesis Research Organization

Employment Type: Full-time | Entry-Level

About Us

ClinoGenesis Research Organization is a premier institute offering clinical research training, placement services, and recruitment solutions. We specialize in shaping skilled professionals for the healthcare and research industries. We are currently hiring freshers for the position of Clinical Research Coordinator (CRC) — a perfect launchpad for your clinical research career.

Role Overview

As a Clinical Research Coordinator, you’ll be responsible for supporting clinical trial operations, managing site-level activities, and ensuring compliance with regulatory protocols. This is an ideal opportunity for fresh life science graduates looking to step into the dynamic world of clinical research.

Key Responsibilities

• Assist in organizing and conducting clinical trials
• Maintain accurate trial records and documents
• Coordinate with investigators, participants, and sponsors
• Ensure compliance with GCP, ICH, and ethical standards
• Support subject recruitment, screening, and follow-up activities
• Manage and track clinical trial data and site documentation

Eligibility Criteria

 ducation: Open to all Life Science graduates and postgraduates, including:

B.Sc./M.Sc. in Life Sciences, Biotechnology, Microbiology, Biochemistry, Genetics, etc.

B.Pharm, M.Pharm, Pharm.D Nursing (B.Sc./M.Sc. Nursing)BPT, MPT, and other health science-related backgrounds

Experience: Freshers only

Skills:

• Excellent communication and coordination skills
• Strong attention to detail and willingness to learn
• Basic understanding of clinical trial processes and ethical guidelines

Why Join ClinoGenesis?

Career launchpad for freshers

Industry-relevant training and real-world exposure

Recruitment and placement support

Work with reputed clinical sites and research sponsors

Apply Now:

Send your updated resume to

Or apply directly via LinkedIn.

• Conduct site initiation, monitoring, and close-out visits in accordance with clinical trial protocols and Standard Operating Procedures (SOPs).
• Verify the accuracy, completeness, and integrity of clinical trial data by reviewing source documents and case report forms (CRFs).
• Ensure compliance with Good Clinical Practice (GCP), FDA regulations, and other applicable guidelines.
• Build and maintain strong working relationships with investigators, site staff, and study sponsors.
• Identify and report any deviations, adverse events, or safety concerns promptly.
• Provide training and ongoing support to clinical trial site personnel.
• Prepare and submit monitoring reports, study status updates, and other required documentation.
• Manage study supplies and investigational product accountability at clinical sites.
• Participate in investigator meetings and other relevant study-related meetings.
• Assist in the selection and qualification of new clinical trial sites.

• Bachelor's degree in Life Sciences, Nursing, Pharmacy, or a related healthcare field. Master's degree preferred.
• Minimum of 3 years of experience as a Clinical Research Associate or in a similar clinical trial monitoring role.
• Thorough understanding of ICH-GCP guidelines and regulatory requirements for clinical trials.
• Experience with electronic data capture (EDC) systems and clinical trial management systems (CTMS).
• Excellent understanding of medical terminology and disease processes.
• Strong organizational, time management, and problem-solving skills.
• Exceptional communication, interpersonal, and presentation skills.
• Ability to travel to clinical sites as required (approximately 50-70% travel).
• Detail-oriented with a commitment to data quality and patient safety.
• Proficiency in English and Gujarati is essential.

• Conduct pre-study, initiation, routine, and close-out monitoring visits at clinical trial sites.
• Verify the accuracy, completeness, and timeliness of clinical data through source data verification.
• Ensure compliance with the investigational plan, protocols, and applicable regulatory requirements (e.g., FDA, ICH GCP).
• Manage communication and relationships with investigators, site staff, and study sponsors.
• Identify, document, and escalate any deviations from protocol or GCP guidelines.
• Oversee drug accountability and ensure proper storage and handling of investigational medicinal products.
• Train site personnel on study-specific procedures and regulatory requirements.
• Prepare monitoring visit reports and follow up on action items.
• Contribute to the development and review of study-related documents, such as protocols and informed consent forms.
• Maintain accurate and up-to-date study documentation in Trial Master Files (TMF).
• Support study start-up activities, including essential document collection and regulatory package preparation.

• Conduct pre-study, initiation, routine, and close-out monitoring visits at clinical trial sites.
• Verify the accuracy, completeness, and integrity of clinical data through source document verification.
• Ensure compliance with study protocols, Standard Operating Procedures (SOPs), GCP, and all applicable regulatory requirements.
• Train and support site staff on study procedures, protocol requirements, and data collection.
• Monitor patient recruitment and retention efforts at assigned sites.
• Manage study supplies and equipment distribution to sites.
• Resolve data discrepancies and queries in a timely manner.
• Prepare monitoring reports and communicate findings and action items to the study team and site personnel.
• Oversee the collection, shipment, and accountability of investigational product and biological samples.
• Build and maintain strong working relationships with investigators, site staff, and internal stakeholders.
• Ensure timely submission of all essential regulatory documents.

• Bachelor's degree in Life Sciences, Nursing, Pharmacy, or a related scientific field.
• Minimum of 3-5 years of experience as a Clinical Research Associate or in a similar clinical trial management role.
• In-depth knowledge of GCP, ICH guidelines, and regulatory requirements for clinical trials.
• Experience with electronic data capture (EDC) systems and clinical trial management systems (CTMS).
• Excellent understanding of medical terminology and clinical trial processes.
• Strong analytical, problem-solving, and critical thinking skills.
• Exceptional organizational, time management, and prioritization abilities.
• Outstanding written and verbal communication skills, with the ability to effectively interact with diverse stakeholders.
• Willingness to travel extensively to clinical trial sites.
• This role offers a Hybrid work arrangement, with significant on-site responsibilities in Bhubaneswar, Odisha and surrounding areas.

• Perform site selection visits to assess the suitability of potential clinical trial sites.
• Initiate study sites, ensuring all necessary documentation and regulatory requirements are met.
• Conduct routine monitoring visits to ensure adherence to protocols, SOPs, and regulatory guidelines.
• Verify the accuracy, completeness, and integrity of clinical trial data.
• Ensure patient safety and rights are protected throughout the study.
• Manage and resolve site issues and discrepancies in a timely manner.
• Prepare site monitoring reports and follow up on action items.
• Facilitate communication between the investigative sites, the study team, and the sponsor.
• Assist with site close-out activities, including the reconciliation of study drug and investigational product.
• Stay current with GCP, FDA regulations, and other relevant guidelines.

• Bachelor's degree in Life Sciences, Nursing, Pharmacy, or a related field.
• Minimum of 3 years of experience as a Clinical Research Associate or in a related clinical trial role.
• In-depth knowledge of GCP, ICH guidelines, and regulatory requirements.
• Proven experience in site monitoring and data verification.
• Excellent organizational, communication, and interpersonal skills.
• Ability to manage multiple projects and sites simultaneously.
• Proficiency in clinical trial management systems (CTMS) and electronic data capture (EDC) systems.
• Willingness to travel to clinical sites as required.
• Strong problem-solving and critical-thinking abilities.

• Perform site selection, initiation, monitoring, and close-out visits in accordance with clinical trial protocols and SOPs.
• Ensure adherence to Good Clinical Practice (GCP) guidelines and all applicable regulatory requirements.
• Verify the accuracy, completeness, and integrity of clinical data by reviewing source documents.
• Oversee the management of investigational product and supplies at study sites.
• Train and support study site staff on protocol requirements, procedures, and data collection.
• Identify, document, and resolve site-level issues and deviations.
• Communicate effectively with investigators, site staff, internal study teams, and regulatory authorities.
• Prepare and present monitoring visit reports in a timely manner.
• Track and manage study-related documentation and regulatory binders.
• Ensure patient safety and data confidentiality are maintained at all times.
• Contribute to the development and review of study protocols and other study documents.
• Participate in investigator meetings and training sessions.

• Bachelor's degree in a life science, nursing, or related healthcare field.
• Minimum of 3 years of experience as a Clinical Research Associate or in a similar clinical trial management role.
• In-depth knowledge of clinical trial processes, GCP, ICH guidelines, and relevant regulatory frameworks.
• Experience with various therapeutic areas is advantageous.
• Strong understanding of medical terminology and clinical trial documentation.
• Excellent monitoring and auditing skills.
• Exceptional organizational, time management, and problem-solving abilities.
• Strong written and verbal communication skills.
• Proficiency in using clinical trial management systems (CTMS) and electronic data capture (EDC) systems.
• Ability to travel to clinical trial sites as required.
• Ability to work effectively in a hybrid environment, balancing remote tasks with on-site visits.