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.

• 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.

• 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.

By joining our team, you'll be part of groundbreaking research that can positively impact the lives of women and children. You'll work in a collaborative and supportive environment where your contributions are valued.

If you’re enthusiastic about taking on this impactful role and contributing to meaningful work, we’d love to hear from you!

Please send your resume and a cover letter detailing your qualifications and motivation to This email address is being protected from spambots. You need JavaScript enabled to view it. .

Be sure to include Paediatrician – Clinical Trial & Community-Based Study in the subject line.

The Health System Liaison Officer is responsible for building and maintaining effective communication between the research team and local health systems. The HSLO officer ensures alignment of the study with local health policies, supports integration with health services, and fosters strong stakeholder relationships to facilitate successful implementation

• 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.

• 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.

By joining our team, you'll be part of groundbreaking research that can positively impact the lives of women and children. You'll work in a collaborative and supportive environment where your contributions are valued.

If you’re enthusiastic about taking on this impactful role and contributing to meaningful work, we’d love to hear from you!

Please send your resume and a cover letter detailing your qualifications and motivation to This email address is being protected from spambots. You need JavaScript enabled to view it. .

Be sure to include Health System Liaison Officer – Clinical Trial & Community Engagement in the subject line.

The Safety Associate will support the implementation and oversight of safety monitoring activities for a clinical trial and community-based study involving human participants. This role ensures that all adverse events (AEs), serious adverse events (SAEs), and other safety signals are properly documented, assessed, reported, and followed up in compliance with Good Clinical Practice (GCP), ethical standards, and regulatory guidelines.

• 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.

• 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.

If you’re enthusiastic about taking on this impactful role and contributing to meaningful work, we’d love to hear from you!

If you're ready to take on this exciting role and make a real difference, we want to hear from you!

Please send your resume and a cover letter detailing your qualifications and motivation to This email address is being protected from spambots. You need JavaScript enabled to view it. .

Be sure to include Safety Associate – Clinical Trial & Community-Based Study in the subject line.

The Study Physician is responsible for conducting clinical assessments, ensuring participant safety, and implementing the clinical aspects of the study according to the protocol. This role involves direct clinical care, adverse event monitoring, and coordination with the broader research team.

• 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.

• MBBS or BAMS degree with valid registration.
• Minimum 1–2 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.

By joining our team, you'll be part of groundbreaking research that can positively impact the lives of women and children. You'll work in a collaborative and supportive environment where your contributions are valued.

If you’re enthusiastic about taking on this impactful role and contributing to meaningful work, we’d love to hear from you!

Please send your resume and a cover letter detailing your qualifications and motivation to This email address is being protected from spambots. You need JavaScript enabled to view it. .

Be sure to include Study Physician (MBBS/BAMS) – Clinical Trial & Community-Based Study in the subject line.

The Project Manager will oversee the planning, execution, and coordination of all aspects of the clinical trial and community-based study. This includes staff management, regulatory compliance, budgeting, timelines, and reporting.

• 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.

• 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.

By joining our team, you'll be part of groundbreaking research that can positively impact the lives of women and children. You'll work in a collaborative and supportive environment where your contributions are valued.

If you’re enthusiastic about taking on this impactful role and contributing to meaningful work, we’d love to hear from you!

Please send your resume and a cover letter detailing your qualifications and motivation to This email address is being protected from spambots. You need JavaScript enabled to view it. .

Be sure to include Project Manager – Clinical Trial & Community-Based Study in the subject line.

The Study Nurse will support clinical trial procedures including screening, enrolment, follow-up, sample collection, and documentation. The role requires interaction with participants and the ability to work in both clinic and field settings.

• 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.

• 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.

By joining our team, you'll be part of groundbreaking research that can positively impact the lives of women and children. You'll work in a collaborative and supportive environment where your contributions are valued.

If you're ready to take on this exciting role and make a real difference, we want to hear from you!

Please send your resume and a cover letter detailing your qualifications and motivation to This email address is being protected from spambots. You need JavaScript enabled to view it. .

Be sure to include Study Nurse – Clinical Trial & Community-Based Study in the subject line.

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.

• 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.

• Bachelor’s degree in Life Sciences, Clinical Research, or related field.
• At least 1–2 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.

By joining our team, you'll be part of groundbreaking research that can positively impact the lives of women and children. You'll work in a collaborative and supportive environment where your contributions are valued.

If you’re enthusiastic about taking on this impactful role and contributing to meaningful work, we’d love to hear from you!

Please send your resume and a cover letter detailing your qualifications and motivation to This email address is being protected from spambots. You need JavaScript enabled to view it. .

Be sure to include Quality Assurance (QA) Officer / Document Officer – Clinical Trial in the subject line.

• CV
• Cover letter explaining your motivation for applying
• Contact information for two academic/professional references

• Master in health science/other biological sciences.
• 4 to 5 years’ experience in public health.

• Master in health science/other biological sciences.
• 4 to 5 years’ experience in public health.

• Master in health science/other biological sciences.
• 1 year experience in community based studies and public health.

• Minimum 12th Pass, able to use computers and iPads
• Minimum 2-3 years of field experience in community based epidemiological studies

• MBBS

• BAMS/BHMS/MD/MS degree with 1 year of experience in general practice or Research. Freshers can also apply

• Graduate/PG in Life Sciences/Pharmacy degree with 2year of experience in relevant subject

• Graduate/PG in Life Sciences/Pharmacy degree with 2year of experience in relevant subject