Clinical Research Jobs in Delhi

Roles & ResponsibilitiesClinical Trial Start-Up• Assist in preparation of study protocols, Investigator’s Brochure, CRFs, and patient information documents• Coordinate with Ethics Committees and Regulatory Authorities for approvals• Conduct site feasibility assessments and support investigator selection• Assist in site initiation and training activitiesTrial Monitoring & Execution• Perform routine on-site monitoring visits• Conduct Source Data Verification (SDV)• Ensure CRF accuracy and regulatory compliance as per ICH-GCP guidelines• Train site staff on study-specific procedures• Manage Investigational Medicinal Product (IMP) accountability• Ensure protocol adherence and subject safetyDocumentation & Close-Out• Prepare monitoring visit reports and follow-up letters• Maintain Trial Master File (TMF) and essential documents• Support audit and inspection readiness• Close trial sites and archive documentation upon study completion• Prepare final reports for sponsors and regulatory authoritiesQualification• Degree in Life Sciences / Medical Sciences / Nursing from a recognized institution• Bachelor of Pharmacy• Master of Pharmacy• Doctor of PharmacyExperience• Minimum 2 years of clinical trial coordination or monitoring experience• Experience in NCD, cardiovascular, or renal trials preferred• Experience in regulatory submissions and ethics committee processesSkills• Strong knowledge of ICH-GCP guidelines• Understanding of regulatory approvals and ethics submissions• Clinical documentation and CRF handling expertise• Site monitoring and stakeholder coordination skills• Willingness to travel for monitoring visits• Excellent English communication and report-writing skillsAbout the OrganizationThe George Institute for Global Health is a globally recognized medical research organization operating in over 40 countries, focused on improving health outcomes worldwide through high-impact research in non-communicable diseases, including cardiovascular, renal, and chronic conditions.

Roles & Responsibilities• Assist in preparation of protocol, Investigator’s Brochure, CRF, and patient information documents• Coordinate with Ethics Committees and Regulatory Authorities for submissions and approvals• Conduct site feasibility assessments and support investigator selection and site initiation• Perform on-site monitoring visits and Source Data Verification (SDV)• Ensure CRF accuracy, regulatory compliance, and adherence to ICH-GCP guidelines• Train site staff on study-specific procedures and protocol requirements• Manage Investigational Medicinal Product (IMP) accountability• Prepare monitoring visit reports and maintain trial documentation• Archive study documents and prepare final reports for sponsors and authorities• Support site close-out activities upon study completionQualification• B.Pharm / M.Pharm / Pharm.D / Life Sciences / Medical Sciences / NursingExperience• Minimum 2 years of clinical trial coordination or clinical research experience• Experience in site monitoring, ethics submissions, and regulatory coordination• Knowledge of ICH-GCP and clinical documentation practicesSkills• Strong understanding of ICH-GCP guidelines and regulatory processes• Experience in CRF handling and clinical documentation management• Ability to coordinate with multi-site stakeholders• Willingness to travel for site monitoring visits• Excellent English communication skills• Strong organizational and time management abilitiesAbout the CompanyThe George Institute for Global Health is a globally recognized medical research organization affiliated with leading universities and operating in more than 40 countries. With a strong focus on non-communicable diseases such as cardiovascular, renal, and chronic disorders, the institute conducts large-scale international clinical trials aimed at improving global health outcomes. It promotes diversity, ethical research standards, and collaborative clinical research excellence.

Roles & Responsibilities:• Conduct and oversee site initiation, interim monitoring, and close-out visits according to study protocols, GCP, and applicable regulatory guidelines• Build and maintain strong professional relationships with investigators, site coordinators, and key stakeholders• Proactively identify and resolve site issues to ensure quality and compliance• Perform comprehensive monitoring visits to assess site performance, data accuracy, and adherence to protocol• Ensure timely follow-up on monitoring findings, query resolution, and documentation in compliance with SOPs• Support risk-based monitoring activities and provide oversight to ensure data reliability• Ensure all trial activities comply with study protocols, SOPs, and local/international regulations• Participate in preparation and review of regulatory submissions and ethics committee communications• Monitor, document, and report adverse events according to safety protocols and regulatory timelines• Collaborate with data management and project teams to maintain high data quality and consistency• Participate in internal and external audits, ensuring readiness and corrective actions as needed• Provide ongoing training, mentoring, and support to site staff and junior CRAs• Serve as a subject matter expert for protocol-related and operational queriesQualification:• Bachelor of Pharmacy, Master of Pharmacy• Bachelor’s or Master’s degree in Life Sciences or a related fieldExperience:• Minimum 3 years as a Clinical Research Associate with demonstrated success in independently managing clinical sitesSkills:• Strong understanding of ICH-GCP, local and international regulatory requirements, and clinical trial conduct• Excellent communication and interpersonal abilities• Strong analytical, organizational, and problem-solving skills• Proficiency in documentation, reporting, and time management• Ability to work independently and collaboratively within cross-functional teams• Willingness to travel extensively to investigative sitesAbout the Organization:MS Clinical Research (MSCR) is a leading clinical research organization dedicated to advancing scientific innovation and improving healthcare outcomes through high-quality clinical trials that meet global standards.

Roles & Responsibilities• Coordinate day-to-day clinical trial activities at the study site• Assist investigators in patient screening, recruitment, and follow-up visits• Maintain and update Trial Master File (TMF) and essential study documents• Ensure compliance with ICH-GCP guidelines and approved study protocols• Support and document the informed consent process• Perform data entry and resolve queries in CRF/eCRF systems• Communicate with sponsors, CROs, and ethics committees• Prepare study reports and maintain regulatory documentation• Support monitoring visits and auditsQualification• B.Sc / M.Sc or equivalent degree in Life Sciences• Master of PharmacyExperience• Minimum 1 year of clinical research experience• Experience in site coordination and clinical trial documentation preferredSkills• Understanding of clinical trial processes• Basic knowledge of ICH-GCP guidelines• Strong documentation skills• Proficiency in CRF/eCRF systems• Good communication and coordination abilities• Attention to detail and compliance awarenessAbout the OrganizationA leading clinical research services provider based in Delhi, India, offering structured clinical trial management solutions. The organization provides strong exposure to clinical operations, regulatory documentation, and sponsor coordination within a professional research environment.

Roles & Responsibilities• Perform site monitoring visits (selection, initiation, monitoring, and close-out visits) in accordance with GCP and ICH guidelines.• Work with sites to drive and track subject recruitment plans to meet project needs and enhance predictability.• Administer protocol and related study training to assigned sites and establish regular communication to manage project expectations and issues.• Evaluate the quality and integrity of study site practices and adherence to regulations, escalating quality issues as necessary.• Track the progress of assigned studies, including regulatory submissions, recruitment, CRF completion, and data query resolution.• Ensure site documents are available for filing in the Trial Master File (TMF) and ensure Investigator's Site File (ISF) is maintained according to GCP/ICH and local requirements.• Create and maintain documentation regarding site management and monitoring visit findings, submitting regular reports and follow-up letters.• Collaborate with study team members for project execution support as needed.• If applicable, support development of site-specific subject recruitment plans and manage site financials per clinical trial agreements.Qualification• Relevant qualification in life sciences, clinical research, or related fields.Experience• 3+ years of relevant experience in Clinical Research.Vacancies• Multiple positions available in Bangalore, Mumbai, Ahmedabad, and Delhi.Skills• Strong knowledge of GCP, ICH, and regulatory guidelines.• Excellent communication and interpersonal skills.• Ability to manage site monitoring, recruitment, and data queries effectively.• Experience with Trial Master File (TMF) and Investigator's Site File (ISF).• Strong organizational skills and ability to track study progress.About the CompanyIQVIA India is a global leader in healthcare data and analytics, providing solutions to help clients in the pharmaceutical, biotechnology, and healthcare industries. IQVIA’s mission is to enable healthcare organizations to navigate complex data, deliver insights, and improve patient outcomes through advanced technology and clinical expertise.

Roles & Responsibilities• Assist Principal Investigator (PI) in site feasibility and study start-up activities• Prepare and maintain regulatory documents (CVs, Financial Disclosure, PI Undertaking, Confidentiality Agreements)• Coordinate IRB/IEC submissions, safety reports, amendments, and progress reports• Support informed consent process and prepare for Site Initiation Visits (SIV)• Maintain Site Master File (SMF), patient files, screening & enrollment logs• Manage patient pre-screening, recruitment, follow-ups, and visit coordination• Ensure accurate CRF completion and clinical data entry• Perform SAE reporting and follow-up activities• Maintain drug accountability and inventory records• Track study budgets, IRB fees, invoices, lab costs, and patient reimbursementsQualification• Any Graduate (Life Sciences / Pharmacy preferred)Experience• 1–4 years of experience in clinical research or clinical trial coordinationSkills• Strong knowledge of ICH-GCP guidelines• Experience in IRB/IEC submissions and regulatory documentation• SAE reporting and drug safety awareness• CRF completion and clinical data management• Patient recruitment and site coordination skills• Good communication, documentation, and organizational abilityAbout the OrganizationMax Healthcare is one of India’s leading hospital networks, known for excellence in patient care and advanced medical research. The organization offers strong exposure to investigator-initiated and sponsored clinical studies within a reputed hospital research environment.

Roles & Responsibilities:• Assist Principal Investigator (PI) in site feasibility assessments• Support pre-trial documentation and regulatory readiness• Collect and maintain updated CVs of site staff• Ensure timely completion of financial disclosure forms, PI undertaking, and confidentiality agreements• Coordinate with IRB/IEC for faster approvals and timely submission of safety reports and protocol amendments• Assist PI & Co-Investigators in Informed Consent Process• Prepare for Site Initiation Visits (SIV)• Maintain Site Master File (SMF) and patient files• Handle patient recruitment, screening, enrollment, and follow-ups• Complete CRF and clinical data entry• Coordinate patient follow-up visits (physical & telephonic)• Report and follow-up on SAE (Serious Adverse Events)• Manage drug accountability and inventory tracking• Maintain study budget sheets and track IRB fees, site administration fees, lab costs, and patient reimbursementsQualification:• B.Pharm, M.Pharm, Pharm.D, Msc, BSc, LifesciencesExperience:• 1–4 years in clinical research / clinical trialsSkills:• Knowledge of ICH-GCP Guidelines• Experience with IRB/IEC Submissions• SAE Reporting & Drug Safety• CRF Completion & Clinical Data Management• Patient Recruitment & Site CoordinationAbout The Company:Max Healthcare is one of India’s leading hospital networks, offering an advanced research ecosystem for clinical trials. The company is focused on providing comprehensive healthcare and pioneering clinical research that adheres to global standards, promoting patient safety and the highest standards of care.

Roles & Responsibilities• Write, review, and edit clinical regulatory documents• Prepare clinical study protocols and clinical study reports (CSRs)• Develop Investigator’s Brochures, ICFs, CRFs, and related documents• Ensure documents comply with ICH-GCP and regulatory guidelines• Coordinate with clinical, regulatory, and cross-functional teams• Maintain accuracy, consistency, and timelines for document delivery• Incorporate reviewer comments and quality checks as requiredQualification• Life Sciences / Pharmacy / Medical postgraduate or equivalent• Strong academic background in clinical research or medical writingExperience• Minimum 5 years of hands-on experience in medical writing• Proven experience with regulatory and clinical documentationSkills• Excellent scientific writing and editing skills• Strong knowledge of ICH-GCP and regulatory standards• Attention to detail and document quality control• Ability to manage multiple projects and deadlines• Good communication and stakeholder coordination skillsAbout the OrganizationCliniExperts Research Services is a global clinical research organization providing end-to-end clinical trial, regulatory, and medical writing services, committed to quality, compliance, and innovation in clinical research.

Roles & Responsibilities: • Conduct clinical trials in compliance with ICH-GCP and protocol guidelines • Support study start-up activities and assist with site initiation • Participate in recruitment and retention of study subjects • Complete and maintain source documents, CRFs, and logs accurately • Compile and update the Site Master File • Manage Investigational Products (IP), including accountability and shipping • Coordinate submissions and communication with the Ethics Committee • Update sponsors on study progress and prepare for monitoring visits • Perform other responsibilities assigned by management Qualifications: • Graduates/postgraduates in Life Sciences, Pharmacy, Biotechnology, or related fields • Freshers with a completed Clinical Research course can also apply Experience: • 2–4 years in clinical research or relevant field (freshers with certification considered) Skills: • Strong interest in clinical trials and regulatory compliance • Excellent organizational, communication, and documentation skills About the Organization: This organization is dedicated to conducting high-quality clinical trials with a focus on regulatory compliance and data integrity. They provide a collaborative environment where professionals can grow their careers in clinical research and contribute to innovative healthcare solutions.

Role & Responsibilities • Maintain accurate and structured patient records including demographics, diagnosis, treatment, and follow-up • Ensure completeness of clinical data covering eligibility, baseline assessments, concomitant medications, and lab/imaging summaries • Track documentation required for program eligibility and continued patient support • Conduct scheduled patient follow-ups (telephonic, virtual, or site-based) • Monitor treatment adherence, compliance, and clinician-reported clinical response • Identify and escalate missed doses, deviations, or safety concerns • Record and track adverse events and serious adverse events in structured formats • Escalate safety signals in line with internal SOPs and pharmacovigilance principles • Coordinate with treating physicians and hospital teams for follow-up data and documentation • Support generation of program reports on patient numbers, compliance trends, and safety observations • Assist in tracking patient eligibility for government health schemes and institutional support programs Qualification • PhD or MSc in Life Sciences, Pharmacy, Biotechnology, or Nursing • MBBS or MD candidates welcome but not mandatory Experience • Prior experience as a Clinical Research Associate preferred • Experience with patient-focused programs or public hospital collaborations desirable • Familiarity with biologic or specialty therapies (oncology, rheumatology, immunology) preferred Skills • Strong clinical documentation and data management skills • Ability to conduct structured patient follow-ups and longitudinal tracking • Basic understanding of pharmacovigilance and safety reporting • Effective communication and coordination with physicians and hospital teams • High attention to detail and data quality • Ability to work collaboratively across internal and external stakeholders About the Company • DAVA Oncology works closely with public hospitals and government medical colleges across India , Focuses on patient access, outcomes tracking, and support programs for advanced therapies