Summary
Overview
Work History
Education
Skills
education history and training
licensure and certification
Timeline
Generic

BEATRICE MBOMEH

Rockwall,TX

Summary

Highly qualified and results driven health care professional with proven track record and success in building strong relationships with patients and clients. Energetic and goal-oriented with an impressive performance record and well-rounded background in optimizing internal performance. Currently seeking a position which will utilize all skills, abilities, and areas of expertise.

Overview

21
21
years of professional experience

Work History

Senior Clinical Research Associate

Thermo Fisher
12.2023 - Current
  • Conduct initiation, monitoring and closeout visits to verify study procedures, regulatory documents and data completion.
  • Improve clinical trial efficiency by streamlining data collection and management processes.
  • Enhance patient safety through meticulous monitoring of adverse events and protocol compliance.
  • Reduce study timelines by effectively managing multiple concurrent clinical trials across various therapeutic areas.
  • Strengthen collaboration with cross-functional teams, ensuring clear communication and alignment on project goals.
  • Perform study drug accountability and reconciliation via Interactive Response Technology and site drug repository.
  • Follow drug storage procedures to comply with protocols and SOP requirements.

Senior Clinical Research Associate

Worldwide Clinical Trials
08.2021 - 12.2023
  • Conducted initiation, monitoring and closeout visits to verify study procedures, regulatory documents and data completion.
  • Improved clinical trial efficiency by streamlining data collection and management processes allowing 100% data cut deadline milestone 2 cycles in a row.
  • Enhanced patient safety through meticulous monitoring of adverse events and protocol compliance decreasing protocol deviations by 40%.
  • Reduced study timelines by effectively managing multiple concurrent clinical trials across various therapeutic areas.
  • Strengthened collaboration with cross-functional teams, ensuring clear communication and alignment on project goals.
  • Performed study drug accountability and reconciliation via Interactive Response Technology and site drug repository.
  • Followed drug storage procedures to comply with protocols and SOP requirements.
  • Developed strong relationships with investigators and site staff, fostering a culture of trust and open communication throughout the study duration.
  • Streamlined vendor management processes for more efficient service delivery in support of clinical trial activities.
  • Provided expert guidance to junior team members, fostering a culture of continuous learning and professional growth.

Senior Clinical Research Associate I

IQVIA
09.2019 - 08.2021
  • Conducted initiation, monitoring and closeout visits to verify study procedures, regulatory documents and data completion.
  • Improved clinical trial efficiency by streamlining data collection and management processes.
  • Enhanced patient safety through meticulous monitoring of adverse events and protocol compliance.
  • Reduced study timelines by effectively managing multiple concurrent clinical trials across various therapeutic areas.
  • Strengthened collaboration with cross-functional teams, ensuring clear communication and alignment on project goals.
  • Played an instrumental role in driving enrollment success by collaborating closely with sites on recruitment strategies tailored to specific patient populations allowing recruitment goal to be met 3 months ahead of schedule.
  • Implemented electronic data capturing systems to adhere with clinical research guidelines.
  • Directed, guided and delegated tasks to teams and developed project schedules, resource requirements and timelines to maintain productivity on goals and objectives.
  • Performed study drug accountability and reconciliation via Interactive Response Technology and site drug repository.
  • Followed drug storage procedures to comply with protocols and SOP requirements.

Clinical Research Associate II

PPD
04.2017 - 06.2019
  • Conducted initiation, monitoring and closeout visits to verify study procedures, regulatory documents and data completion.
  • Improved patient enrollment by developing and implementing effective recruitment strategies.
  • Enhanced data quality by closely monitoring study progress and ensuring accurate data collection.
  • Streamlined clinical trial processes for increased efficiency, utilizing strong organizational skills.
  • Collaborated with cross-functional teams to successfully meet project timelines and deliverables.
  • Performed study drug accountability and reconciliation
  • Followed drug storage procedures to comply with protocols and SOP requirements.

Clinical Research Associate

Quintiles
09.2015 - 04.2017
  • Conducted initiation, monitoring and closeout visits to verify study procedures, regulatory documents and data completion.
  • Improved patient enrollment by developing and implementing effective recruitment strategies.
  • Enhanced data quality by closely monitoring study progress and ensuring accurate data collection.
  • Streamlined clinical trial processes for increased efficiency, utilizing strong organizational skills.
  • Collaborated with cross-functional teams to successfully meet project timelines and deliverables.
  • Performed study drug accountability and reconciliation
  • Followed drug storage procedures to comply with protocols and SOP requirements.

Clinical Trials Assistant

Quintiles
03.2014 - 09.2015
  • Streamlined clinical trial documentation by efficiently organizing and maintaining accurate records.
  • Assisted in the successful completion of various clinical trials by providing timely support to research teams.
  • Ensured smooth trial progress with meticulous attention to detail in data entry and record-keeping tasks.
  • Coordinated patient visits, managing schedules for optimal efficiency and adherence to trial protocols.
  • Supported the preparation of Investigational New Drug applications, expediting review processes for new treatments.
  • Managed inventory of study supplies, minimizing delays due to shortages or expired materials.
  • Contributed to continuous improvement efforts by participating actively in training programs and staying up-to-date on industry best practices.
  • Answered telephone calls to offer office information, answer questions, and direct calls to staff.
  • Collaborated with medical and administrative personnel to maintain patient-focused, engaging and compassionate environment.

Certified Pharmacy Technician

OptumRx
05.2011 - 12.2013
  • Improved patient satisfaction by efficiently processing prescriptions and managing inventory in a timely manner.
  • Enhanced pharmacy workflow by assisting pharmacists with medication dispensing, labeling, and packaging.
  • Streamlined prescription processing with accurate data entry and verification of patient information.
  • Reduced medication errors by diligently cross-checking medications against patients'' profiles before dispensing.
  • Boosted customer loyalty by providing friendly, knowledgeable assistance on drug interactions and side effects.
  • Maximized pharmacy efficiency through effective communication with staff members and adherence to procedures.
  • Assisted in maintaining a clean and organized work environment, ensuring compliance with safety regulations.
  • Contributed to the reduction of prescription wait times by promptly addressing refill requests and insurance authorizations.
  • Expedited insurance claim resolutions by liaising with healthcare providers and insurance companies on patients'' behalf.
  • Promoted patient confidentiality by adhering to HIPAA regulations when handling personal information during transactions.
  • Assisted in training new team members on standard operating procedures to ensure consistent quality of service across the entire team.
  • Answered incoming phone calls and addressed questions from customers and healthcare providers.
  • Stocked, labeled, and inventoried medication to keep accurate records.
  • Counted and labeled prescriptions with correct item and quantity.
  • Entered and processed patients' prescriptions into internal system.
  • Performed wide range of pharmacy operations with strong commitment to accuracy, efficiency and service quality.

Direct Support Professional

Help at Home
12.2010 - 11.2012
  • Enhanced quality of life for individuals with disabilities by providing compassionate and consistent direct support.
  • Assisted clients in achieving personal goals through tailored care plans and daily skill-building activities.
  • Maintained a safe and inclusive environment by addressing behavioral challenges with patience and understanding.
  • Collaborated with interdisciplinary teams to develop comprehensive support strategies for each client''s unique needs.
  • Monitored medication administration, maintaining accurate records to ensure client safety and compliance with prescribed treatment plans.
  • Provided ongoing communication between clients, families, and other service providers to enhance overall care coordination efforts.
  • Adapted support approaches based on individual client preferences, fostering increased trust and rapport over time.
  • Administered medication as directed by physician.
  • Built and maintained rapport with clients and family members to facilitate trusting caregiver relationship.

Pharmacy Technician

Rockhill LTC Pharmacy
07.2009 - 12.2010
  • Worked under the direct supervision of a licensed pharmacist; assisting with dispensing medication according to the prescription
  • Staged and generated manifest for cycle exchange, assist in bagging and boxing drugs according to the facility procedures
  • Assisted in processing returned drugs and recycle/dispose per procedure.
  • Assisted in preparing E-kits
  • Assisted in pre-packing frequently ordered medications, label, and store, as needed during low volume pharmacist.


Laboratory Technician

Cleveland Chiropractic College
08.2005 - 12.2008
  • Enhanced laboratory efficiency by implementing new testing procedures and protocols.
  • Streamlined sample processing for faster turnaround times, resulting in improved customer satisfaction.
  • Maintained a high level of accuracy in test results by following strict quality control procedures.
  • Assisted in the development of new laboratory methods, leading to increased testing capabilities.
  • Increased sample throughput by optimizing workflow and efficient use of resources.
  • Prepared detailed documentation for each experiment, facilitating effective communication of results to colleagues and stakeholders.
  • Reduced errors in data entry by meticulously reviewing and validating information before submission.
  • Supported regulatory compliance efforts through adherence to guidelines and thorough record-keeping practices.
  • Contributed to a safe working environment by consistently following established safety procedures and guidelines within the lab setting.

Certified Pharmacy Technician

Eckerd Drug
02.2003 - 08.2005
  • Assisted in preparation, distribution and storage of pharmaceuticals.
  • Maintained drug inventory levels by ordering necessary medications and supplies.
  • Communicated with prescribers to verify medication dosages, refill authorizations, and patient information.
  • Collected co-payments or full payments from customers.
  • Communicated directly with doctors offices via telephone, fax and email.
  • Maintained proper drug storage procedures, registries, and records for controlled drugs.
  • Helped pharmacist clear problematic prescriptions and address customer questions to keep pharmacy efficient.
  • Reviewed and verified customer information and insurance provider information.
  • Stocked, labeled, and inventoried medication to keep accurate records.
  • Consulted with insurance company representatives to complete claims processing, resolve concerns, and reconcile payments.
  • Answered incoming phone calls and addressed questions from customers and healthcare providers.
  • Streamlined pharmacy operations through effective organization of supplies, workspace layout optimization, and process improvements.

Education

Bachelor of Science - Human Biology

Cleveland Chiropractic College
Kansas City
2008

Skills

  • Medical terminology fluency
  • Conflict resolution abilities
  • Data management proficiency
  • Attention to detail
  • Problem-solving aptitude
  • Medication Dispensing
  • Records Maintenance
  • Quality Assurance
  • Organizational capabilities
  • Regulatory compliance knowledge
  • Adverse event reporting
  • Multitasking abilities
  • Social Support
  • Dietary Guidelines
  • Supporting Daily Living Needs
  • Meal Planning and Preparation
  • Activities of Daily Living (ADLs)
  • Medical Chart Documentation
  • Personal Hygiene Support

education history and training

B.S. in Human Biology, Cleveland Chiropractic College

licensure and certification

  • TX Registered Pharmacy Technician- license# 365526
  • Certified Pharmacy Technician, PTCB# 30257754

Timeline

Senior Clinical Research Associate

Thermo Fisher
12.2023 - Current

Senior Clinical Research Associate

Worldwide Clinical Trials
08.2021 - 12.2023

Senior Clinical Research Associate I

IQVIA
09.2019 - 08.2021

Clinical Research Associate II

PPD
04.2017 - 06.2019

Clinical Research Associate

Quintiles
09.2015 - 04.2017

Clinical Trials Assistant

Quintiles
03.2014 - 09.2015

Certified Pharmacy Technician

OptumRx
05.2011 - 12.2013

Direct Support Professional

Help at Home
12.2010 - 11.2012

Pharmacy Technician

Rockhill LTC Pharmacy
07.2009 - 12.2010

Laboratory Technician

Cleveland Chiropractic College
08.2005 - 12.2008

Certified Pharmacy Technician

Eckerd Drug
02.2003 - 08.2005

Bachelor of Science - Human Biology

Cleveland Chiropractic College
BEATRICE MBOMEH