142 Clinical Research Associates jobs in Bengaluru

• Coordinate and manage multiple clinical research studies simultaneously, ensuring compliance with protocols and regulatory requirements (GCP, ICH).
• Recruit, screen, and enroll study participants, ensuring informed consent processes are thoroughly explained and documented.
• Collect, process, and maintain accurate study data, adhering to strict data integrity and confidentiality standards.
• Administer study medications and perform research procedures as required by the protocol.
• Monitor participant adherence to study protocols and provide ongoing participant education and support.
• Manage study-related supplies, equipment, and investigational products.
• Prepare for and participate in internal and external monitoring visits and audits.
• Liaise with principal investigators, sub-investigators, study sponsors, and regulatory agencies.
• Contribute to the development of study protocols, informed consent forms, and other study-related documents.
• Train and mentor junior research staff, providing guidance on study conduct and best practices.
• Ensure timely submission of all required documentation and reports.
• Maintain organized and accurate research records, both electronic and paper-based.
• Assist with budget management and resource allocation for research studies.
• Identify potential challenges and develop proactive solutions to ensure smooth study progression.

• Bachelor's degree in Nursing, Life Sciences, Health Sciences, or a related field. A Master's degree or relevant certifications (e.g., CCRP, CCRA) are highly preferred.
• Minimum of 5-7 years of direct experience as a Clinical Research Coordinator.
• In-depth knowledge of Good Clinical Practice (GCP) guidelines and regulatory requirements for clinical trials.
• Proven experience with participant recruitment, informed consent, and data management.
• Proficiency in electronic data capture (EDC) systems and clinical trial management systems (CTMS).
• Excellent organizational, time management, and multitasking skills.
• Strong attention to detail and commitment to accuracy.
• Effective communication and interpersonal skills for interacting with participants, medical staff, and sponsors.
• Ability to work independently and as part of a collaborative team.
• Experience in leading or supervising junior research staff is a significant advantage.
• Basic understanding of medical terminology and clinical procedures.

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

Job Title : Clinical Research Associate (CRA)

Company : MS Clinical Research Pvt Ltd

Experience : Minimum 3 years

About Us :

MS Clinical Research (MSCR) is a leading clinical research organization dedicated to advancing scientific discovery and improving healthcare outcomes. We are committed to conducting high-quality clinical trials and contributing to the development of innovative medical solutions.

Job Summary :

We are seeking a highly motivated and experienced Clinical Research Associate (CRA) with a minimum of 3-5 years of relevant experience. The CRA will play a critical role in ensuring the successful planning, execution, and monitoring of clinical trials. The ideal candidate will have a strong understanding of clinical trial processes, regulatory requirements, and excellent communication and organizational skills.

Key Responsibilities :

Site Management :

Conduct site initiation, routine monitoring, and close-out visits to ensure compliance with the study protocol, Good Clinical Practice (GCP), and regulatory requirements. Build and maintain strong relationships with investigative sites, investigators, and study coordinators.

Clinical Trial Monitoring :

Perform routine monitoring visits to assess site performance, data integrity, and regulatory compliance. Ensure timely resolution of data queries and issues identified during monitoring visits.

Protocol Compliance :

Ensure that all study activities are conducted in accordance with the approved protocol, SOPs, and applicable regulatory guidelines. Collaborate with investigators to address and resolve protocol-related queries.

Regulatory Compliance :

Assist in the preparation and submission of regulatory documents to ethics committees and regulatory authorities. Stay informed about changes in regulatory requirements and update study teams accordingly.

Data Management :

Collaborate with data management teams to ensure accurate and timely data collection and entry.

Perform source data verification and data validation activities.

Safety Reporting :

Monitor and report adverse events in compliance with regulatory requirements and safety reporting procedures. Ensure that safety reports are submitted to relevant authorities and stakeholders.

Training and Support :

Provide training and support to site staff on study protocols, data collection, and regulatory compliance. Act as a resource for investigators and site staff throughout the duration of the study.

Requirements :

Education: Bachelor's degree in a relevant life sciences field.

Experience :

Minimum of 3 years of experience as a Clinical Research Associate.

Proven track record of successful site management and monitoring in clinical trials.

Regulatory Knowledge: Familiarity with regulatory requirements and guidelines governing clinical trials.

Communication Skills : Excellent verbal and written communication skills.

Organizational Skills : Strong organizational and time management skills with attention to detail.

Team Collaboration : Ability to work effectively in cross-functional teams and independently.

Travel : Willingness to travel to investigative sites as needed.

Benefits :

Competitive salary and benefits package.

Opportunities for professional development and advancement.

Collaborative and dynamic work environment.

Join our team at MS Clinical Research and contribute to the advancement of clinical research and the development of innovative healthcare solutions.

CRA Job Opening @ ICON – Bangalore.

ICON plc is hiring Clinical Research Associates (CRA) in Bangalore Be part of a global leader in healthcare intelligence & clinical research.

Know someone perfect for this?

Choudhary Waseem Jamil

Job Types: Full-time, Fresher

Pay: ₹100, ₹500,000.00 per year

Benefits:

• Internet reimbursement

Work Location: In person

Company Description

Novaspire Biosciences Private Limited is a healthcare company specializing in Pharmacovigilance, Clinical Research, and Bioavailability/Bioequivalence studies Project Management support. Novaspire is dedicated to enhancing patient safety and promoting public health through innovative solutions for the pharmaceutical and biotechnology industries. Our team of experienced professionals provides a wide range of services, including Pharmacovigilance, Clinical Research Consulting, and Regulatory Affairs Solutions.

Objectives of this role

• Ensuring compliance with protocols, standard operating procedures, and Good Clinical Practice (GCP) guidelines.
• Conducting regular site visits to monitor trial activities and data collection.
• Reviewing and analysing clinical trial data for accuracy and completeness.
• Developing and maintaining study timelines and budgets.
• Providing training to study staff on study protocols and GCP guidelines.

Your tasks

• Reviewing and approving study-related documents, such as informed consent forms.
• Conducting source data verification and ensuring data quality.
• Managing trial supplies and drug accountability.
• Serving as a liaison between study sites, sponsors and regulatory agencies.

Required skills and qualifications

• bachelor's/Master's degree in pharmacy.
• At least 1 year of experience in a similar role.
• Knowledge of regulatory requirements and guidelines, such as Good Clinical Practice (GCP) and International Council for Harmonization (ICH).
• Certification in clinical research, such as the Association of Clinical Research Professionals (ACRP) certification.
• Knowledge of clinical trial data management systems and electronic data capture.
• Experience with site selection, initiation, management, and monitoring activities.
• Strong attention to detail and accuracy in data management.

Preferred skills and qualifications

• Understanding of pharmacology and drug development processes.
• Working knowledge of medical terminology and anatomy.
• Excellent project management and leadership skills with attention to detail.
• Ability to work collaboratively with study teams and cross-functional departments

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 (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

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.