151 Clinical Research Associates jobs in Bengaluru
Clinical Research Coordinator(Fresher)
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Clinical Research Coordinator (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 Coordinators.
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
Job Type: Fresher
Pay: Up to ₹30,000.00 per month
Work Location: In person
Clinical Research
Posted today
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Job Description
Overview:
Dozee Health AI is a pioneer in Contactless Remote Patient Monitoring (RPM), proven to drive transformation at scale. Headquartered in Bengaluru, India, Dozee has emerged as India's no. 1 RPM Company.
We are seeking visionary individuals to help us in this very exciting journey. As a part of our dynamic team, you'll have the opportunity to collaborate with top healthcare providers in the country, applying AI-powered RPM solutions to tackle some of the most pressing challenges in healthcare - enhancing staff efficiency, improving patient outcomes, and pioneering the next generation of care models.
Responsibilities
- Effective execution of clinical studies in hospitals by coordinating and overseeing various study activities, such as, data collection, and monitoring
- Collaborate with investigators and study sites to ensure compliance with study protocols and regulatory standards
- Installation/troubleshooting Dozee devices and train nurses, doctors on Dozee and the patient monitoring dashboard
- Liaising with doctors/consultants or investigators on conducting the clinical study
- Setting up the study site, which includes ensuring the site has the trial materials.
- Verifying of collected study data
- Reviewing case report form and adverse events.
- Supporting the Clinical Research team/Operations in overall management of the assigned studies.
- Providing study status updates to team members and project management and facilitating project timelines.
- Maintaining study related Files and collection of the essential documents and project related documents.
- Coordinate with remote team and inform about activities conducted during the visit
- Build and manage relationship with nurses, doctors, floor in charges etc
Requirements
- Degree (Graduation or Post Graduation) in science or pharmacy (BE/BSc/BDS/ B.Pharm/ M. Pharm/ M.Sc ) with 0-1 years of experience
- Excellent written and verbal communication skills in English, Marathi and Hindi
- Understanding of using Google cloud products, and MS Office
- Good planning, organization and problem-solving abilities
- Ability to work with minimal supervision
- Ability to work in teams
- Ability to manage multiple priorities
- Willingness to work in flexible schedules/shifts.
Good to have
- Experience/Exposure in Healthcare space
₹10,000 - ₹15,000 a month
Vision & Mission
Save Million lives with Health AI
Dozee is India's leading AI-Powered
contactless Remote Patient Monitoring (RPM)
and
Early Warning System (EWS).
A solution that continuously monitors patients and provides early warnings of clinical deterioration, enabling timely interventions and enhancing patient safety in hospitals, nursing facilities and patient homes. A
"Made in India for the World"
solution, Dozee has pioneered the world's first non-contact blood pressure monitoring system. Trusted by leading healthcare providers in India, the USA, and Africa, Dozee is transforming patient safety and care by enhancing outcomes and reducing costs.
Dozee is adopted by
300+ hospitals
and
monitors beds across 4 countries
. Dozee has monitored over
1 Mn Patients,
Delivered
35000+ Life Saving Alerts
and Saved
10 Mn+ Nursing Hours.
Videos
- Science Behind Dozee : Ballistocardiography & Artificial Intelligence
- 100 Dozee deliver 144 life saving alerts and INR 2.7 Cr of saving - Sattva Study
- Dozee saves life of a mother at home
- Leading Healthcare Game changers work with Dozee I
- I ntroducing Dozee VS
- Dozee Shravan - A clinical grade RPM service
Dozee In News
Bloomberg - Oct 21, 2024
From AI Beds to Remote ICUs, Startups are plugging India's health Gaps
News18Oct 26, 2024
Now, You Can Remotely Monitor Your Loved Ones in Hospital With Bengaluru Start-Up's 'Shravan'
Analytics India MagazineOct 29, 2024
Dozee Harness AI for Personalised Patient Care
ET HealthWorldSep 16, 2024
We trust AI everyday - From Google Maps to Smartphones, So why not use it to enhance patient safety in healthcare?
BW healthcareworldOct 29, 2024
Dozee's AI-Powered System Predicts Patient Deterioration 16 Hours in Advance
A tertiary care hospital study published in
JMIR
, validated Dozee's Early Warning System (EWS), showing it
identified 97% of deteriorating patients, provided alerts ~19 hours in advance
, and generated
5x fewer alerts,
reducing alarm fatigue and improving patient outcomes.
A study at King George Medical University, Lucknow, and published in
Frontiers in Medical Technology
demonstrated that Dozee's automation can potentially save
2.5 hours of nursing time per shift
, improving workflow efficiency and allowing more focus on patient care.
A study on remote patient monitoring in general wards published in
Cureus
found that
90%+ of healthcare providers reported improved care
and patient safety,
74% of patients felt safer
, and there was a
43% increase in time for direct patient care.
Research by
Sattva
, an independent consulting firm, demonstrates Dozee's substantial impact: for every 100 Dozee-connected beds, it can
save approximately 144 lives
,
reduce nurses' time for vital checks by 80%
, and
decrease ICU average length of stay by 1.3 days.
Key Highlights
- Founded : October, 2015
- Founders : Mudit Dandwate, Gaurav Parchani
- Headquarters : Bangalore, India | Houston, USA | Dubai, UAE
- Key Investors & Backers : Prime Ventures, 3one4 Capital, YourNest Capital, Gokul Rajaram, BIRAC (Department of Biotechnology, State Bank of India, and Dinesh Mody Ventures, Temasek Foundation, Horizons Ventures
- Stage : Series A+
- Team Strength : 280+
- Business : Providing Continuum of care with AI-powered contactless Remote Patient Monitoring (RPM) and Early Warning System (EWS) for Hospitals and Home.
- Certifications & Accreditations : ISO13485:2016 Certified, ISO27001:2022 Certified, CDSCO Registered, FDA510K Cleared for the flagship product Dozee Vitals Signs (VS) measurement system and SOC2 Type II Certified
Achievements
- Forbes India 30 under 30
- Forbes Asia 100 to Watch
- Times Network - India Health Awards 2024 for AI innovation in Bharat Healthcare tech
- BML Munjal Award for Business Excellence using Learning and Development
- FICCI Digital Innovation in Healthcare Award
- Anjani Mashelkar Inclusive Innovation Award Marico Innovation For India Award.
To know more about ,
click here
.
Disclaimer:
Dozee is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees." Dozee does not discriminate on the basis of race, religion, color, sex, gender identity, sexual orientation, age, non-disqualifying physical or mental disability, national origin, veteran status or any other basis covered by appropriate law. All employment is decided on the basis of qualifications, merit, and business need. Dozee will not tolerate discrimination or harassment based on any of these characteristics
Clinical Research
Posted today
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Job Description
Job Title: Clinical Research Trainer
Experience: Minimum 3 years in Clinical Research Training / Clinical Research domain
Location: CliniLaunch Research Institute - Bangalore, 56/18 & 55/9 Ozone Manay Technology Park, 3rd Floor, Hosur Main Road, Service Rd, Garvebhavi Palya, Bengaluru, Karnataka
Job Type: Full-time | Immediate Joiner
Responsibilities:
- Conduct training sessions on Clinical Research concepts, GCP, and industry practices.
- Design and deliver effective training modules and assessments.
- Mentor and guide trainees through practical and theoretical sessions.
- Evaluate trainee performance and provide constructive feedback.
Requirements:
- Bachelor's/Master's degree in Life Sciences or related field.
- Strong knowledge of Clinical Research, GCP, and regulatory guidelines.
- Excellent communication and presentation skills.
Interested candidates can apply immediately
Job Type: Full-time
Pay: ₹40, ₹70,000.00 per month
Benefits:
- Cell phone reimbursement
- Health insurance
- Paid sick time
- Provident Fund
Expected Start Date: 20/10/2025
Clinical Research Associate
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Job Description
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 today
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Job Description
Junior Role (6months - 4 years)
Locations : Delhi And Bangalore
1) Author and analyze clinical trial documents.
2 )Work with key clinical documents: Protocol, Informed Consent Form, Clinical Study Report,
3) Summary of Clinical Safety/Efficacy, Access Evidence Dossier, Statistical Analysis Plan and more.
4) Create, validate, and refine prompts for AI-assisted document generation.
5 )Apply knowledge of clinical trial phases, study design, and drug development.
6 )Maintain compliance with global regulatory standards (FDA, EMA, ICH-GCP).
7) Ensure quality control and timely delivery of assigned tasks.
8) Collaborate with cross-functional teams to improve document accuracy and prompt effectiveness.
9) Provide regular updates and flag risks to the project manager.
Clinical Research Associate
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Job Description
Assist in planning, initiation, and execution of clinical trials.
Conduct site monitoring visits and ensure adherence to study protocols, SOPs, and regulatory requirements.
Please call / for further details.
Clinical Research Associate
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Job Description
Responsibilities & functions: Clinical Research Associate
- Working in accordance with ICH E6 principles and with applicable SOPs (either ECRON AcuNova or Sponsor's SOPs) & local regulatory norms.
- Review of study synopsis.
- Site selection.
- Preparation of Site feasibility questionnaire, conducting the feasibility and reporting to PM.
- Preparation, conduct and reporting of site selection visits.
- Negotiation & obtaining Investigator agreement on site budget, payment to the sites.
- Development/Local adaptation of study specific documents (ICF, CRF prints, Study logs), translations of the documents.
- Procuring essential documents from sites, their QC and filing in a timely manner and updating project tracker or sending the documents to PA for filing in a timely manner.
- Maintenance of TMF and Site specific file.
- Scanning & uploading documents into shared drive.
- Transmission of documentation into project files.
- Preparation of regulatory dossier, regulatory submission and follow-up.
- Preparation of EC dossier, EC submissions and follow-up.
- Co-ordinating arrangements for the investigators meeting, acting as a host for this meeting.
- Development of meeting materials along with required presentations for investigators meeting.
- Site initiation visit planning, preparation, conduct, report and follow-up of pending issues.
- Co-ordinating the IP request between sites and pharmacist/vendor/sponsor.
- Site monitoring visit planning, preparation, conduct, report and follow-up of pending issues.
- Remote Monitoring, Central Monitoring and Risk Based Monitoring related activities.
- Accompanied visit as a part of mentoring a new CRA.
- Interacting with DM for data transfer and query resolution.
- Interacting with MW for CSR appendices.
- Preparation of project status report.
- Preparations, participation in meetings and documentation of meeting minutes.
- Provide oversight to project (maintaining quality & timelines of deliverables).
- Participate in client QA assessments.
- Reconciliation Filing of project correspondence.
- Site close-out visit planning, preparation, conduct, report.
- Maintenance of Investigator database and a QC of the database.
- Archival of study documentation. Participation in other department initiatives/activities.
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Clinical Research Associate
Posted today
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Job Description
Clinical Research Coordinator (Freshers Only)
Location: (Bangalore 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 Coordinators.
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
Job Types: Full-time, Fresher
Pay: ₹231, ₹1,125,530.70 per year
Benefits:
- Commuter assistance
- Internet reimbursement
Work Location: In person
Clinical Research Associate
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Job Description
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 .