Bhargavi Dhamarlapally
Shamshabad
Summary
To join a reputed and growth-oriented health organization where I could utilize my medical knowledge and good patient serving skills to improve client satisfaction for the benefit of organization and self. Dedicated clinical research coordinator experienced in complying with study protocols, standard operating procedures and good clinical practices. Practiced problem-solver with strong attention to detail. Prepared to offer several years' experience in the field and take on a fast-paced position.
Overview
2
2
years of professional experience
1
1
Certification
Work History
Clinical Research Coordinator
KIMS Hospitals
Secunderabad
12.2024 - Current
- Currently working as Clinical research coordinator in kims Hospitals minister road Secunderabad.
- Coordinated clinical trial activities in compliance with regulatory guidelines.
- Managed patient recruitment and informed consent processes for studies.
- Facilitated communication between investigators, sponsors, and study participants.
- Monitored participant safety and reported adverse events promptly.
- Organized site visits and prepared materials for regulatory audits.
- Trained new staff on clinical research procedures and practices.
- Maintained accurate databases for tracking study progress and data collection.
- Communicated effectively with investigators, study staff, sponsors, vendors, IRB personnel, and other stakeholders throughout the life cycle of the trial.
- Maintained accurate up-to-date tracking logs for all aspects of clinical research activities including but not limited to adverse events, serious adverse events, concomitant medications, lab results .
- Monitored patient safety during clinical trials according to established guidelines.
- Collaborated with internal departments such as Regulatory Affairs and Data Management to ensure that all studies were conducted in accordance with ICH-GCP guidelines.
- Organized investigator meetings; developed meeting agendas; created presentations; tracked action items from meetings; coordinated follow-up communications after meetings.
- Performed patient assessments, collected and analyzed data, and prepared reports.
- Educated participants on studies and anticipated outcomes.
Trainee Clinical Research Coordinator
Gleneagles Clinical Research Services
06.2023 - 08.2024
- Worked as Trainee clinical research coordinator for 1year 3months in Gleneagles clinical research services.
- Had experience of Clinical research coordinator for 1year 3 months.
- Worked on both Indian and Global clinical trials.
- Worked on multiple clinical trials in General medicine, critical care, pulmonology, cardiology, Gastroenterology, Orthopedics, Gynecology departments.
- Ability to work on multiple clinical trials.
- Assisted in coordinating clinical trials and ensuring compliance with protocols.
- Maintained accurate records of participant information and study documentation.
- Assisted in the development of project timelines including milestones and deadlines while adhering to Good Clinical Practices.
- Monitored subject recruitment and ensured compliance with applicable laws and regulations.
- Maintained accurate records of all clinical trial activities and updated databases accordingly.
- Assisted in the preparation of research protocols, informed consent forms, and other study documents.
- Coordinated between multiple departments within the organization to ensure smooth functioning of research operations.
- Collected, processed and delivered specimens from trial participants.
Education
PHARM D - DOCTOR OF PHARMACY
Chilkur Balaji College of pharmacy
Hyderabad01.2024
Intermediate -
Sri chaitanya college
Hyderabad01.2018
SSC -
Narayana Concept School
Hyderabad01.2016
Skills
- Microsoft Word
- Excel
- PowerPoint
- Outlook
- Team player
- Verbal communication
- Written communication
- Project management
- EDC Capture
- Data entry
- Data management
- Clinical trials
- ICH GCP Guidelines
- IWRS
- Clinical applications
- Patient counselling
- Pharmacovigilance
- Regulatory compliance
- Clinical trial coordination
- Adverse event reporting
- Problem resolution
- Staff training
- Good clinical practices
- Informed consent process
- Clinical trial management
- Documentation requirements
- Investigator coordination
- Specimen handling
- Research experience
- Scheduling proficiency
- Laboratory results management
- Adverse event tracking
- Investigational product management
- Patient education
- Problem-solving aptitude
- Decision-making
- Records management
- Multitasking Abilities
Certificates And Activities
- ICH-GCP Certification
- Participated in various seminars and workshops
- International symposium on medication safety and clinical pharmacy, Continental Hospitals, Hyderabad, Telangana, India, 2023
- 25th annual national convention of the association of pharmaceutical teachers of India, JSS College of Pharmacy, JSS Academy of Higher Education and Research, Mysuru, India, 2022
- Scientific sessions of AICTE sponsored International conference, Bhaskar Pharmacy College, Hyderabad, Telangana, India, 2020
Projects
A cross-sectional study on incidence of contrast induced nephropathy / AKI in the patients undergoing percutaneous coronary intervention using Mehran risk score
Disclaimer
I hereby declare that the above information contained herein is true and correct to the best of my knowledge and belief.
Job Description
- Conducting trails according to protocols and responsible for organizing the documentation and files
- Experience in assessing Serious Adverse effects for clinical/investigational drugs
- Working effectively with focus and great attention using experience knowledge of ICH-GCP guidelines and regulations governing clinical trial practice
- Seeking a job to learn and broaden the knowledge and methodology and to enhance and utilize the skill in reputed organization
- I would like the organization to enable me to grow professionally and allow me to perform at the best of my potential with the company and I will also make a positive contribution towards your company
Certification
- Certified Clinical Research Coordinator (CRC) Internship Certificate – Gleneagles Clinical Research Services
• E3 GCP Certification
• ICH-GCP Certification
• Investigator Meeting (IM) – SOS-AMI Study
• iMedidata Platform Training
- Attended an international symposium on medication safety and clinical pharmacy at Continental Hospitals, Hyderabad, Telangana, India, 2023
- Attended the 25th annual national convention of the Association of Pharmaceutical Teachers of India 2022, held at JSS College of Pharmacy, JSS Academy of Higher Education and Research, Mysuru, India
- Attended the scientific sessions of the AICTE-sponsored international conference organized by Bhaskar Pharmacy College, Hyderabad, Telangana, India, in 2020
Areas Of Interest
- Clinical Trial Management
- GCP & ICH Compliance
- Site Coordination & Monitoring Support
- SAE Reporting & Documentation
- Regulatory Submissions
Timeline
Clinical Research Coordinator
KIMS Hospitals
12.2024 - Current
Trainee Clinical Research Coordinator
Gleneagles Clinical Research Services
06.2023 - 08.2024
PHARM D - DOCTOR OF PHARMACY
Chilkur Balaji College of pharmacy
Intermediate -
Sri chaitanya college
SSC -
Narayana Concept School