244 Medical Research jobs in Bengaluru
Medical writing / research analyst
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Social Worker (Delhi Office – Healthcare Programs) Location: New Delhi | Full-time | 50% Travel RequiredAbout Jiv Daya FoundationJiv Daya Foundation (JDF) is a U. S.-based private foundation committed to improving the quality of life for underserved populations. In India, JDF supports several healthcare programs, including Tuberculosis, Rheumatology, Maternal and Neonatal Health, and Eye Care Initiatives. Our programs are implemented in collaboration with government hospitals, academic institutions, and local partners.About the RoleWe are looking for a passionate and organized Social Worker to join our Delhi-based office. This position will work across multiple healthcare initiatives—primarily Tuberculosis and Rheumatology initiative—to support patient engagement, access to care, and coordination with treatment centers. The role requires frequent field travel (~50%) to government hospitals and patient homes in and around Delhi.Key ResponsibilitiesSupport TB and Rheumatology patients with treatment adherence, follow-up, and emotional counseling.Assist patients in applying for government and non-government aid programs at both state and central levels.Help patients and caregivers with documentation, form submissions, and navigating official processes for availing treatment support.Create and maintain a repository of state and national-level patient assistance schemes and health entitlements.Track and follow up with patients regularly to ensure continuity of care and linkage to appropriate support programs.Coordinate with hospital social work departments, government agencies, and NGOs to ensure patient needs are addressed.Identify and build a local donor network, including individuals and community-based groups, willing to support patients financially or in-kind.Maintain accurate patient records, gather field-level insights, and contribute to regular reporting and documentation.Assist in field logistics, coordination with healthcare staff, and support day-to-day project operations.Required QualificationsMaster’s degree in Social Work, Public Health, or a related field. Graduates from institutions like TISS, PHFI, or similar are strongly encouraged to apply.2–4 years of relevant experience in healthcare-related social work or public health programs.
Medical writing / research analyst
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Medical Writing / Research Analyst
Posted 9 days ago
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Location: New Delhi | Full-time | 50% Travel Required
About Jiv Daya Foundation
Jiv Daya Foundation (JDF) is a U.S.-based private foundation committed to improving the quality of life for underserved populations. In India, JDF supports several healthcare programs, including Tuberculosis, Rheumatology, Maternal and Neonatal Health, and Eye Care Initiatives. Our programs are implemented in collaboration with government hospitals, academic institutions, and local partners.
About the Role
We are looking for a passionate and organized Social Worker to join our Delhi-based office. This position will work across multiple healthcare initiatives—primarily Tuberculosis and Rheumatology initiative—to support patient engagement, access to care, and coordination with treatment centers. The role requires frequent field travel (~50%) to government hospitals and patient homes in and around Delhi.
Key Responsibilities
- Support TB and Rheumatology patients with treatment adherence, follow-up, and emotional counseling.
- Assist patients in applying for government and non-government aid programs at both state and central levels.
- Help patients and caregivers with documentation, form submissions, and navigating official processes for availing treatment support.
- Create and maintain a repository of state and national-level patient assistance schemes and health entitlements.
- Track and follow up with patients regularly to ensure continuity of care and linkage to appropriate support programs.
- Coordinate with hospital social work departments, government agencies, and NGOs to ensure patient needs are addressed.
- Identify and build a local donor network, including individuals and community-based groups, willing to support patients financially or in-kind.
- Maintain accurate patient records, gather field-level insights, and contribute to regular reporting and documentation.
- Assist in field logistics, coordination with healthcare staff, and support day-to-day project operations.
Required Qualifications
Master’s degree in Social Work, Public Health, or a related field- .Graduates from institutions like TISS, PHFI, or similar are strongly encouraged to apply
- .2–4 years of relevant experience in healthcare-related social work or public health programs
Healthcare Research & Data Analyst
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About Clarivate
Who are you?
What will you do?
What do you know?
Requirements:
Skills:
Education:
Preferred (Good to have) skills:
Work Mode: Hybrid, Monday to Friday 12:00 pm to 8:00 pm
At Clarivate, we are committed to providing equal employment opportunities for all qualified persons with respect to hiring, compensation, promotion, training, and other terms, conditions, and privileges of employment. We comply with applicable laws and regulations governing non-discrimination in all locations.
Senior Healthcare Research & Data Analyst
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We are looking for a Senior Analyst to join our Medtech Data team at Clarivate Bangalore.This is an amazing opportunity to work on market research (including both primary and secondary research), competitive analysis, clinical trial analysis, financial analysis, forecasting, insight generations, produce comprehensive market research reports and conduct custom consulting projects for medical devices and healthcare markets.
What will you be doing in this role?
About You – experience, education, skills, and
About the Team
The team consists of around 40 colleagues spread across teams in India and is reporting to the respective team managers. We have a great skill set in the market research and consulting domain related to medical devices & healthcare markets and we would love to speak with you if you have skills or interest for the same.
Hours of Work
Hybrid work mode, working days Monday to Friday, working hours 12:00 PM IST to 9:00 PM IST, Hybrid working mode.
At Clarivate, we are committed to providing equal employment opportunities for all qualified persons with respect to hiring, compensation, promotion, training, and other terms, conditions, and privileges of employment. We comply with applicable laws and regulations governing non-discrimination in all locations.
Associate Healthcare Research & Data Analyst
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We are looking for an Associate Healthcare Research and Data Analyst to join our Medtech Insights team in Bengaluru, India. This is an amazing opportunity to work on market research (including both primary and secondary research), competitive analysis, clinical trial analysis, financial analysis, forecasting, insight generations, produce comprehensive market research reports and conduct custom consulting projects for medical devices and healthcare markets. The team consists of around 25 colleagues spread across 3 teams in India and is reporting to the respective team managers. We have a great skill set in the market research and consulting domain related to medical devices and healthcare markets and we would love to speak with you if you have skills or interest for the same.
About You – experience, education, skills, and accomplishments
It would be great if you also had . . .
What will you be doing in this role?
About the Team
The Medtech Insights team is group of subject matter experts and is mainly responsible to produce Medtech 360 syndicated market research reports and conduct custom consulting projects, related to medical device markets. Medtech Insights team harnesses real-world healthcare data, in-depth interviews, and our unique mix of in-house expertise to help medical device companies make some of their most important business decisions. The team is spread across 3 locations: Toronto, Canada; Bengaluru, India; and Barcelona, Spain.
Hours of Work
Hybrid work mode. The work timing is 12 – 9PM IST. This helps the team to have some overlap with their counterparts working in other offices in Toronto and Barcelona.
At Clarivate, we are committed to providing equal employment opportunities for all qualified persons with respect to hiring, compensation, promotion, training, and other terms, conditions, and privileges of employment. We comply with applicable laws and regulations governing non-discrimination in all locations.
Jobs For Clinical Research Associate-Medical & Clinical Industry- Bangalore, Bengaluru, Karnataka...
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JOB DETAILS
1. Ensure thatclinical researchstudies are conducted in accordance with the protocol, standard operating procedures, goodclinicalpractice (GCP) guidelines, and other applicable regulatory requirements.
2. Perform site selection, initiation, monitoring and close-out visits in accordance with contracted scope of work and GCP guidelines.
3. Review informed consent document / procedures.
4. Negotiate study budgets with potential investigators and assists with the execution of site contracts Provide monitoring visits and site management for a variety of protocols, sites
5. Administer protocol and other study-related training to assigned site personnel and establish regular lines of communication with the sites to manage ongoing project expectations and issues.
6. Evaluate the quality and integrity of the practices of the study site related to the proper conduct of the protocol and adherence to applicable regulations.
7. Escalate quality issues to the CPM / line manager, as deemed necessary.
8. Ensure accurate data reporting via review of site source documents and medical records.
9. Interpret data to identify protocol deviations and risks to subject safety/data integrity.
10. Perform investigational product accountability as per the protocol and Study Monitoring Plan.
FUNCTIONAL AREA
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Senior Clinical Research Scientist - Oncology
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Clinical Research Associate
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Clinical Research Associate (Freshers Only)
Location : (Insert City or "Across India" if remote/hybrid)
Organization: Clinogenesis Research Organization
Department: Clinical operations
Type: Full-Time
About the Role:
Clinogenesis Research Organization is offering an excellent opportunity for fresh graduates to launch their careers as Clinical Research Associate.
Please note: This position is strictly for freshers. Candidates with prior experience are not eligible for this role.
If you’re passionate about clinical research and eager to grow in a structured, accredited environment, we invite you to apply.
Key Responsibilities:
- Assist with on-site coordination of clinical trial activities under supervision
- Maintain essential documents, site files, and case report forms
- Support the investigator in protocol compliance and patient coordination
- Ensure all trial activities adhere to ICH-GCP and ethical guidelines
- Participate in training sessions and team meetings as part of learning
Eligibility Criteria:
- Education: , B pharma , M pharma, B.Sc / M.Sc in Life Sciences, Pharmacy, Nursing, or equivalent healthcare field
- Experience: Freshers only
- Strong communication and organizational skills
- Eagerness to learn and grow in the clinical research domain
Why Start at Clinogenesis?
- Work alongside expert mentors and gain practical exposure
- Structured learning in a globally accredited research setup
- Continuous development and support for long-term career growth
Clinical Research Associate
Posted 1 day ago
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Clinical Research Associate (Freshers Only)
Location: (Insert City or "Across India" if remote/hybrid)
Organization: Clinogenesis Research Organization
Department: Clinical operations
Type: Full-Time
About the Role:
Clinogenesis Research Organization is offering an excellent opportunity for fresh graduates to launch their careers as Clinical Research Associate.
Please note: This position is strictly for freshers. Candidates with prior experience are not eligible for this role.
If you’re passionate about clinical research and eager to grow in a structured, accredited environment, we invite you to apply.
Key Responsibilities:
- Assist with on-site coordination of clinical trial activities under supervision
- Maintain essential documents, site files, and case report forms
- Support the investigator in protocol compliance and patient coordination
- Ensure all trial activities adhere to ICH-GCP and ethical guidelines
- Participate in training sessions and team meetings as part of learning
Eligibility Criteria:
- Education: , B pharma , M pharma, B.Sc / M.Sc in Life Sciences, Pharmacy, Nursing, or equivalent healthcare field
- Experience: Freshers only
- Strong communication and organizational skills
- Eagerness to learn and grow in the clinical research domain
Why Start at Clinogenesis?
- Work alongside expert mentors and gain practical exposure
- Structured learning in a globally accredited research setup
- Continuous development and support for long-term career growth