Salma Badran
Houston,TX
Summary
Detail-oriented Clinical Research Coordinator with proven success in improving data accuracy and regulatory compliance. Skilled in patient recruitment and project management, demonstrating strong problem-solving and organizational abilities.
Overview
2
2
Languages
8
8
years of professional experience
Work History
Clinical Research Coordinator
UC DAVIS MIND INSTITUTE
Sacramento, CA
09.2021 - 05.2022
- Implemented quality control measures, improving data accuracy and reducing discrepancies in reporting processes.
- Collaborated with cross-functional teams to streamline project timelines and enhance communication across stakeholders.
- Led regular team meetings to assess project progress, address challenges, and align on strategic objectives for studies.
- Worked with principal investigator and sponsors to facilitate daily trial activities and comply with research protocols.
- Facilitated clear communication between principal investigators, sponsors, and study participants for seamless trial execution.
- Managed patient recruitment, informed consent process and data entry to support trial objectives.
- Collected data and followed research protocols, operations manuals, and case report form requirements.
- Maintained compliance with regulatory guidelines through rigorous documentation and protocol adherence.
- Improved data integrity and accuracy with meticulous oversight of data collection processes.
Clinical Research Coordinator
UC Davis Health
Sacramento, CA
01.2019 - 05.2022
- Coordinated clinical trial activities to ensure adherence to regulatory guidelines and protocols.
- Managed patient recruitment efforts, enhancing enrollment efficiency through targeted outreach strategies.
- Developed and maintained study documentation, ensuring accuracy and compliance with institutional standards.
- Conducted data collection and analysis, contributing to the integrity of research findings and publications.
- Trained and mentored junior staff on clinical procedures and best practices for study execution.
- Trained new team members on essential clinical research protocols and procedures, promoting a culture of continuous learning.
- Maintained compliance with protocols covering patient care and clinical trial operations.
- Increased participant retention rates through proactive follow-up efforts and regular engagement activities.
- Developed and maintained accurate and up-to-date case report forms and source documents.
- Prepared and maintained regulatory documents for clinical trial submissions.
Assistant Clinical Research Coordinator
California Heart and Vein Specialist
Huntington Beach, CA
06.2016 - 06.2018
- Coordinated clinical trial logistics, including site selection and patient recruitment efforts.
- Collaborated with principal investigators to streamline study workflows and improve efficiency.
- Conducted regular monitoring visits to verify adherence to protocol and safety standards.
- Followed clinical research protocols and conducted study visits in compliance with ICH/GCP and FDA regulations.
- Screened patient records, databases, and physician referrals to identify prospective candidates for research studies.
- Gathered, processed, and shipped lab specimens.
- Followed informed consent processes and maintained records.
- Enhanced patient safety by meticulously monitoring and documenting adverse events during clinical trials.
- Collaborated with clinical staff and other healthcare professionals to support clinical trial data accuracy.
- Coordinated and monitored clinical trial activities to support timely and accurate completion of studies.
- Assessed patients'' eligibility criteria following strict adherence to inclusion/exclusion guidelines.
Caregiver
NS Care
Fountain Valley, CA
06.2014 - 06.2016
- Assisted clients with daily living activities, ensuring comfort and safety.
- Supported medication management by accurately administering prescribed dosages.
- Communicated effectively with healthcare professionals to update client care plans.
- Maintained cleanliness and organization in client living spaces to promote health.
- Developed strong relationships with clients, fostering trust and engagement.
- Documented client progress and changes in health status for review.
- Adapted care techniques based on individual client needs and preferences.
- Trained new caregivers on best practices for patient care and safety protocols.
- Assisted clients with activities of daily living, promoting independence and quality of life.
- Cleaned house, ran errands, managed laundry, and completed weekly grocery shopping.
- Assisted with dressing guidance, grooming, meal preparation, and medication reminders.
- Performed light housekeeping duties to maintain cleanliness standards while respecting the patient''s personal space.
Education
Bachelor of Science - Nursing
Stanbridge University
Irvine, CASkills
- Good clinical practices
- Electronic data capture
- Documentation management
- Informed consent
- Adverse event reporting
- Informed consent process
- Study protocols
- Patient recruitment
- Investigational product management
- Trial management
- Data collection techniques
- Records maintenance
- Participant screening
- Phlebotomy
- Specimen collections
- Medication dispensing
- Subject retention strategies
- Adverse event tracking
- Investigator coordination
- Participant recruitment
- Case report management
- Time management
- Problem-solving
- Teamwork and collaboration
- Multitasking Abilities
- Organizational skills
- Critical thinking
- Data management
- Interpersonal communication
- Written communication
- Task prioritization
- Attention to detail
- Reliability
Languages
Arabic
Native or Bilingual
English
Native or Bilingual
Timeline
Clinical Research Coordinator
UC DAVIS MIND INSTITUTE
09.2021 - 05.2022
Clinical Research Coordinator
UC Davis Health
01.2019 - 05.2022
Assistant Clinical Research Coordinator
California Heart and Vein Specialist
06.2016 - 06.2018
Caregiver
NS Care
06.2014 - 06.2016
Bachelor of Science - Nursing
Stanbridge University