Conduct eligibility screening and physical examinations of study participants. Obtain informed consent and explain study procedures to participants. Monitor participant safety, identify adverse events, and report as per protocol. Prescribe treatment or interventions as required under the study protocol. Ensure proper documentation of clinical assessments in Case Report Forms (CRFs). Participate in protocol training and team meetings. Maintain high ethical standards in dealing with human subjects. Coordinate with field and lab teams for follow-ups and data/sample collection. Qualifications: MBBS or BAMS degree with valid registration. Minimum 12 years of clinical experience, preferably with research or trial exposure. Understanding of Good Clinical Practice (GCP) and research ethics. Ability to work in community and field-based settings, willing to travel within the study area. Good communication and clinical documentation skills
Develop project workplans, timelines, and deliverables. Oversee daily operations across clinical and field teams. Manage communication between study sites, stakeholders, and sponsors. Ensure protocol adherence and quality data collection. Monitor study milestones, track performance, and resolve bottlenecks. Prepare periodic progress reports and assist with regulatory documentation. Lead team meetings and ensure timely dissemination of updates. Ensure compliance with GCP and ethical standards. Qualifications: Master?s degree in Public Health, Life Sciences, Clinical Research, or equivalent. Minimum 3-5 years of project management experience, preferably in health research. Strong leadership, communication, and organizational skills. Familiarity with regulatory and ethical requirements of clinical trials. Proficient in MS Office and project management tools
Serve as the main point of contact between the study team and health system stakeholders (e.g., health facilities, district health offices, health ministries). Coordinate integration of study activities with existing health services and ensure alignment with local policies and programs. Facilitate regular meetings with health authorities to provide updates and address challenges. Support capacity building and training of local health personnel as needed. Assist in identifying and resolving health system barriers to study implementation. Provide input on community engagement strategies and health messaging. Document stakeholder interactions and provide regular reports to the project team. Support ethical and regulatory approvals by liaising with local institutions. Qualifications: Bachelor's or Master?s degree in Public Health, Health Administration, or related field. Experience working with government health systems, NGOs, or public health programs. At least 3 years of experience in health program coordination or stakeholder engagement. Strong interpersonal, negotiation, and communication skills. Knowledge of local health systems, referral pathways, and public health policies. Ability to travel within the study area and work across diverse communities.
Monitor and document all adverse events (AEs) and serious adverse events (SAEs) in accordance with study protocol, sponsor requirements, and applicable regulations. Ensure timely and accurate reporting of SAEs to the Ethics Committee, Sponsor, and Regulatory Authorities as required. Assist clinical staff in the identification, documentation, and classification of safety events. Maintain up-to-date safety tracking logs and ensure proper storage of safety documentation. Participate in safety review meetings and contribute to the preparation of safety summaries and reports. Liaise with investigators, data managers, and monitors to reconcile discrepancies related to safety data. Assist with training site staff on AE/SAE reporting procedures and safety protocols. Support pharmacovigilance and risk management activities, as applicable. Contribute to the development and maintenance of the Safety Management Plan (SMP). Stay updated on evolving safety regulations and ensure compliance at all levels. Qualifications: Bachelor s degree in Pharmacy, Life Sciences, Public Health, or a related field. Minimum 1 2 years of experience in clinical research safety monitoring. Familiarity with Good Clinical Practice (GCP), ICH guidelines, and local regulatory reporting requirements. Experience with safety databases and electronic data capture (EDC) systems is an asset. Strong attention to detail and organizational skills. Effective written and verbal communication skills. Ability to work collaboratively in a multidisciplinary team and across multiple sites
Preparation of study clinic on clinic day. Record vital signs, medical histories, and assist in clinical assessments. Administer medications or interventions as per protocol. Collect, label, and transport biological samples as needed. Keeping track of all the emergency drugs and medicines. Dispense and administer IP and post observation. Appropriate completion of source document, relevant logs/forms for study clinic activities. Provide information and counselling to the Participants regarding use of clinical trial supplies, immediate reporting of AE/ SAE to study team, next scheduled study .clinic visit procedures, emergency contact numbers and appropriate filling of DC. Help to document quality data regarding AEs, SAEs and IAEs. Maintain CRFs and study documents during Clinics. Monitor participants post-intervention and report any adverse events. Maintain confidentiality and adhere to study protocols. Qualifications: ANM/GNM or BSc in Nursing with registration from a recognized body. Minimum 1 year of clinical experience; research experience is a plus. Good interpersonal skills and ability to work in diverse settings. Familiarity with clinical trial procedures and infection control
The QA/Document Officer will ensure that all study activities are conducted according to SOPs, protocols, and regulatory standards. This role is also responsible for managing documentation, version control, and quality audits. Key Responsibilities: Ensure compliance with GCP, SOPs, and study protocols. Maintain a master file of all essential study documents (ISF, TMF). Track approvals, amendments, and site communications. Conduct routine internal audits and quality checks. Prepare for external audits or monitoring visits. Ensure timely archival and retrieval of documents. Support training and version control of SOPs and logs. Qualifications: Bachelors degree in Life Sciences, Clinical Research, or related field. At least 12 years of experience in QA or clinical trial documentation. Familiarity with ICH-GCP and regulatory requirements. Strong organizational skills and attention to detail. Proficient in document management systems and MS Office.
We are seeking a qualified and experienced Paediatrician to support clinical activities in a paediatric-focused clinical trial and community-based health study. The Paediatrician will play a central role in participant assessment, monitoring safety, managing clinical care, and contributing to data quality and protocol adherence. Key Responsibilities: Conduct clinical evaluations and physical examinations of paediatric participants. Assess eligibility and screen potential participants according to protocol criteria. Monitor participant health throughout the study and manage adverse events as per Good Clinical Practice (GCP). Prescribe treatments and interventions per protocol and standard pediatric care guidelines. Collaborate with the clinical trial team including nurses, coordinators, and data managers. Ensure all clinical activities are documented accurately and promptly in Case Report Forms (CRFs) and Electronic Data Capture (EDC) systems. Contribute to training sessions and community awareness initiatives as needed. Maintain confidentiality and uphold ethical standards of paediatric care. Participate in safety monitoring meetings and provide clinical insights to the research team. Qualifications: Medical degree (MBBS or equivalent) with specialization in Paediatrics (MD/DCH). Valid medical license to practice. Minimum 3 years of experience in paediatric clinical practice; experience in research or clinical trials is an asset. Familiarity with GCP and clinical research ethics. Strong communication skills, especially with children and families. Ability to work with multidisciplinary teams in both clinical and community settings and willing to travel within the study area.
Number of Positions – 02 Qualifications MD or DNB Medicine Experience 0 – 1 Year Job Description To work as a SR in the Department of Medicine at a busy tertiary care hospital. To assist in Consultant OPDs, carry out IPD rounds, attend to emergencies, keep Consultants updated about patients, teach junior residents and Medical Officers and carry out Academic activities
Number of Positions 02 Qualifications MD or DNB Medicine Experience 0 1 Year Job Description To work as a SR in the Department of Medicine at a busy tertiary care hospital, To assist in Consultant OPDs, carry out IPD rounds, attend to emergencies, keep Consultants updated about patients, teach junior residents and Medical Officers and carry out Academic activities
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