Ronisha Rivers
Eastern Clinical Research
New Orleans,USA
15
years of professional experience
A highly motivated and self-driven employee, and a devoted medical professional ready to serve the community.
A Professional with experience in clinical research coordination, equipped to make a significant impact in this field. Demonstrates ability to manage clinical trials, ensure compliance with protocols, and maintain accurate documentation. Strong emphasis on team collaboration, reliability, and adaptability to evolving project requirements. Proficient in patient recruitment, data collection, and regulatory submissions, with a results-driven approach that ensures successful study outcomes.
Work History
Clinical Research Coordinator
2 Years 9 Months- Coordinated clinical trial activities, ensuring compliance with regulatory standards and protocols.
- Managed participant recruitment and retention strategies to enhance trial enrollment rates.
- Developed and maintained study documentation, including informed consent forms and case report forms.
- Oversaw data collection processes, ensuring accuracy and integrity of research findings.
- Trained and mentored junior staff on clinical trial procedures and best practices.
- Implemented process improvements to streamline operations and enhance overall efficiency of studies.
- Led site visits to ensure adherence to Good Clinical Practice (GCP) guidelines during trials.
- 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.
- Enhanced patient safety by meticulously monitoring and documenting adverse events during clinical trials.
- Followed informed consent processes and maintained records.
- Collaborated with clinical staff and other healthcare professionals to support clinical trial data accuracy.
- Worked with principal investigator and sponsors to facilitate daily trial activities and comply with research protocols.
- Managed patient recruitment, informed consent process and data entry to support trial objectives.
- Prepared and maintained regulatory documents for clinical trial submissions.
- Oversaw the management of investigational product supplies, ensuring appropriate storage conditions were maintained at all times for optimal efficacy during trials.
- Participated in initiation visits and investigator meetings, implementing trials following study timelines and budgets.
- 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.
- 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.
- Facilitated communication between research teams, investigators, and external stakeholders for seamless project execution.
Pharmacy Technician
12 Years 3 Months- Assist patients by greeting them via phone or in person with their healthcare needs and concerns
- Assisted healthcare providers with incoming faxes and medication requests to ensure timely access to needed treatments
- Actively and consistently maintaining pharmacy inventory to determine the stock level inventory such as what medication and supplies are needed
- Actively and consistently maintain pharmacy inventory to determine the stock level inventory such as what medication and supplies are needed
- Prepares medications for delivery to patients and departments
- Adhere to policies and protocols when it comes to patient confidentiality
- Assist healthcare providers with inquiries such as incoming faxes and requests for medications
- Resolved insurance disputes and provided patients with financial assistance options to facilitate access to medications
- Identified medication requirements needing special storage, including hazardous and refrigerated medications.
- Identifying medication requirements that need special attention or special storage needs such as hazardous medications or refrigerated medications
- Adhering to policies and protocols when it comes to patient confidentiality
- Maintaining a sanitary work environment by sterilizing all work stations and patient areas
- Assist calling other healthcare facilities and/or doctor offices for prescription refill authorizations
Education
Cosmetology School - Cosmetology
Associate of Science - Pharmacy
Skills
HIPAA
Reporting and Electronic Data Entry
Policies and Protocols
Effective Communication
Collaboration and Teamwork
Customer Service
Good clinical practice
Data analysis
Investigational product management
Clinical trial management
Phlebotomy
Specimen collection & handling
Case report management
CLINICAL RESEARCH EXPERIENCE
- CONTRACEPTION
- Myovant/ Sumitomo MVT-601-050: A Phase 3, Single-Arm, Open-Label Study to Evaluate the Safety and Contraceptive Efficacy of Relugolix Combination Therapy in Women with Uterine Fibroids or Endometriosis Who Are 18 to 50 Years of Age and at Risk for Pregnancy “SERENE”
- Excelits CF113-303: A Phase 3, Multi-Center, Non-Comparative Study to Evaluate the Contraceptive Efficacy, Safety, and Tolerability of LPRI-CF113 Administered Orally for 13 Medication Cycles
- DYSPAREUNIA
- Novum 71836003 A Randomized, Double-Blind, Placebo-Controlled, Parallel-Design, Multiple-Site Study to Evaluate the Therapeutic Equivalence of Estradiol Vaginal Inserts 4 mcg (Teva Pharmaceuticals, Inc.) with IMVEXXY (estradiol vaginal inserts) (TherapeuticsMD, Inc.) in the Treatment of Dyspareunia in Women with Vulvar and Vaginal Atrophy.
- BONE DENSITY/ CONTRACEPTION
- Myovant/ Sumitomo MVT-601A-006: A Phase 3B, Single-Arm, Open-Label Study to Evaluate Bone Mineral Density with Long-Term Use of Relugolix Combination Tablet in Premenopausal Women with Heavy Menstrual Bleeding Associated with Uterine Fibroids or Moderate to Severe Pain Associated with Endometriosis “MOXIE”
- VMS/ HOT FLASHES
- Astellas VMS-2693-MA-3457 Astellas Pharma Global Development, Inc. / “A Phase IV, Longitudinal, Observational Study Examining Real World Outcomes of Non-Hormonal Pharmacotherapies Among Individuals Treated for Bothersome Vasomotor Symptoms”
- URINARY TRACT INFECTION
- Iterum IT001-310 A prospective, Phase 3, randomized, multi-center, double-blind study of the efficacy, tolerability, and safety of oral sulopenem etzadroxil/probenecid versus oral amoxicillin/clavulanate for treatment of uncomplicated urinary tract infections (uUTI) in adult women.
Timeline
Clinical Research Coordinator
Eastern Clinical Research
11.2023 - CurrentRead More
Pharmacy Technician
Walmart
08.2011 - 11.2023Read More
Blue Cliff College
Cosmetology School from Cosmetology
Read More
Louisiana Technical College
Associate of Science from Pharmacy
Read More