Versatile clinical research professional knowledgeable about coordinating patient information, laboratory samples and compliance documents for diverse clinical trials. Highly organized and thorough with good planning and problem-solving abilities.
Overview
13
13
years of professional experience
1
1
Certification
Work History
Patient Recruitment Coordinator (Clinical Trials)
Alliance Clinical Network
01.2024 - Current
Maintained strict adherence to study protocols, contributing to high-quality trial Recruitment outcomes and meeting deadlines.
Maintained strong understanding of industry trends and regulatory updates, ensuring clinical trials remained compliant with evolving requirements.
Enhanced patient recruitment by developing and implementing targeted strategies.
Conducted rigorous pre-screening assessments of potential trial participants, ensuring eligibility criteria were met.
Maintained excellent communication with study participants, fostering positive rapport and improving retention rates.
Answered telephone calls to offer office information, answer questions, and direct calls to staff.
Collected and documented patient medical information such as height, weight, and diagnosis.
Qualifying and Scheduling potential study participants for prescreen visits.
Patient Access Representative
Staten Island University Hospital
12.2021 - 12.2023
Facilitated smooth admissions process for patients by pre-registering them, providing clear instructions, and answering their inquiries promptly.
Streamlined referral processes by establishing strong partnerships with healthcare providers, enabling more efficient transfers of patients between facilities.
Improved patient satisfaction by streamlining registration process and reducing wait times.
Secured patient information and confidential medical records in compliance with HIPAA privacy rule standards to protect patient's privacy.
Collected and entered patient demographic and insurance data into computer database to establish patient's medical record.
Utilized knowledge of electronic medical record systems and medical terminology to perform diverse data entry tasks.
Participated in continuous improvement initiatives, collaborating with team members to identify areas of opportunity and develop plans for enhancement.
Managed high volumes of inbound calls while addressing transfer requests, admissions, consults, discharges, prescriptions, and general inquiries professionally.
Adapted quickly to changing demands within the healthcare environment, demonstrating flexibility and a strong commitment to quality patient care.
Trained new team members on department procedures, policies, and software systems, ensuring consistent quality patient care delivery from all team members.
Clinical Research Coordinator
Benmoore Research Center
02.2014 - 04.2016
Managed informed consent process to clearly communicate risks, benefits, expectations, rights and responsibilities related to participation in clinical trials.
Increased participant retention rates through proactive follow-up efforts and regular engagement activities.
Assessed patients' eligibility criteria following strict adherence to inclusion/exclusion criteria.
Enhanced patient safety by meticulously monitoring and documenting adverse events during clinical trials.
Streamlined data collection processes for increased efficiency and accuracy in study results.
Facilitated clear communication between principal investigators, sponsors, and study participants for seamless trial execution
Contributed to the successful completion of clinical trials by proactively resolving issues, mitigating risks, and meeting deadlines in a fast-paced environment.
Oversaw the management of investigational product supplies, temperature excursion, and ensuring appropriate storage conditions were maintained at all times for optimal efficacy during trials.
Screened patient records, databases, and physician referrals to identify prospective candidates for research studies
Research and Development Intern
Neimeth Pharmaceuticals (Pfizer)
06.2011 - 06.2013
Assisted in R&D Projects through stages of product development and ensure compliance.
Collection of samples, specimens for testing, and documentation of results in accordance to SOPs and GCP.
Collaborated with cross-functional teams to ensure alignment on project objectives and deliverables.
Streamlined the R&D process for increased efficiency and reduced project completion time.
Produced reports of findings and gave presentations of results.
Streamlined testing processes for increased efficiency, utilizing automated equipment and advanced testing techniques.
Developed comprehensive reports detailing test results, findings, and recommendations for improvements when necessary.
Enhanced product quality by conducting thorough lab tests and analyses on raw materials and finished products.
Performed routine maintenance and calibration on testing equipment.
Performed Production line quality checks and reviews.
Education
Bachelor of Science - Biochemistry
Imo State University
Owerri
Skills
Proficient in Microsoft office suite
Proficient in Electronic medical record (EMR)
Data Entry
HIPAA Regulations
Attention to details
Study Protocols
Patient Care
Good Clinical Practices
Informed consent
Attention to Detail
Multitasking
Organizational Skills
Accomplishments
Clinical Research Accelerated Training/ Internship - American Carolina Clinical Research, Charlotte, NC May 2023
Certification
ICH GOOD CLINICAL PRACTICE (ICH/GCP)
TRANSPORTATION OF DANGEROUS GOODS (IATA)
Timeline
Patient Recruitment Coordinator (Clinical Trials)
Alliance Clinical Network
01.2024 - Current
Patient Access Representative
Staten Island University Hospital
12.2021 - 12.2023
Clinical Research Coordinator
Benmoore Research Center
02.2014 - 04.2016
Research and Development Intern
Neimeth Pharmaceuticals (Pfizer)
06.2011 - 06.2013
Bachelor of Science - Biochemistry
Imo State University
ICH GOOD CLINICAL PRACTICE (ICH/GCP)
TRANSPORTATION OF DANGEROUS GOODS (IATA)
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