Summary
Overview
Work History
Education
Skills
Websites
Accomplishments
Certification
soccer and medicine.
Timeline
Work Availability
Work Preference
Generic

FRANKLIN IBADIN

MD
Glen Burnie,MD

Summary

Analytical Clinical Research Associate with talents in project development and screening to document and report clinical study progress. Coordinates and facilitate research activities and submits protocols for regulatory approval. Serves as point-of-contact for clinical research professionals and coordinates lab samples to compile detailed data.

Overview

5
5

Clinical Research Associate

2
2

Clinical Care Coordinator

Work History

Clinical Care Coordinator

Essen Medical Associates P.C
08.2023 - Current
  • I conduct daily activities and duties by organizing and assessing all aspects of clinical delivery
  • I help coordinate patient care plans by liaising with different departments and ensuring compliance with official standards
  • I collect and input data and other related information in the system
  • I help coordinate follow-up appointments and referrals to patients specialists as needed.
  • Coordinated, monitored, assigned, and documented patient and clinical care activities.
  • Set up educational programs for clinical staff to enhance skills and knowledge.
  • Built strong relationships with patients and families for optimized care satisfaction.
  • Oversaw quality assurance programs to enhance performance and consistently achieve superior care standards.
  • Mentored new clinical staff members for proper onboarding and orientation processes.
  • Devised and implemented clinical protocols to ensure high-quality patient care.
  • Presented feedback on current and new procedures at weekly clinical meetings.
  • Organized systems for tracking patient records to improve ease of retrieval.
  • Led physicians, nurses and healthcare teams in providing punctual, professional care delivery.
  • Upheld quality assurance procedures to maintain patient safety and satisfaction.
  • Implemented new policies and educated staff on changes.
  • Created weekly schedules for nurses, taking into account sick days and vacation time.
  • Enabled timely service reimbursements by liaising with insurance companies.
  • Assessed clinical policies and procedures for compliance with changing regulations.
  • Created customized care plans, working with hospital staff and families to assess and meet individual needs.
  • Established and maintained effective communication with staff, physicians and community organizations to promote high quality patient care.
  • Liaised with other healthcare professionals to develop comprehensive patient care plans and provide highest quality of care.
  • Scheduled surgeries, managed pre-certifications and verified insurance coverage.
  • Developed and updated policies and procedures, maintaining compliance with guidelines relating to HIPAA, benefits administration and general liability.
  • Implemented successful healthcare program through professionalism, quality of care, medical teaching and patient satisfaction.
  • Ordered all pharmacy supplies and kept check on inventory levels.
  • Successfully negotiated client contract renewals to create increased revenue.
  • Monitored and inspected staff processes to eliminate hazards posed for both residents and staff while ensuring continuous compliance with regulations.
  • Discussed medical histories with patients in effort to provide most effective medical advice.
  • Conducted routine facility inspections, identifying areas needing improvement and eliminating hazards posed to staff and residents for continued compliance with associated regulations.
  • Communicated with patients, ensuring that medical information was kept private.
  • Defined testing protocols, quality assurance initiatives and clinic policies and procedures.
  • Collaborated with store manager to maintain daily operations.

Sr Certified Research Associate

Southern Biotech
04.2018 - 09.2022
  • I have conducted several clinical researches and monitored trials undertaken in record time
  • I have advocated for the advancement of a critical strategic mapping aiming at promoting managerial portfolios
  • I am an observant and a curious collaborator willing to assist in any capacity
  • I am able to exhibit a robust planning and organizational skill set which can be of value to the company
  • I am very capable of covering a very wide range of travel, performing on-site monitoring visits/site selection
  • I have a vast knowledge of pharmaceutical trials, concepts, and terminologies and good practice in clinical developmental applications
  • I have been involved with developing project-specific monitoring plans through evaluating project risk and the FDA guidance
  • I have been involved with monitoring several multiple clinical trials managing and handling functional projects
  • I have helped manage and monitor general/specific sites, ensure compliance was met, and take care of potential risk challenges
  • I have conducted and overseen valuable insight and oversight for evaluation of site performance using accurate data compiled from data management centers as well as other DAID contractors
  • I have developed a clinical trial for 176 patients with chronic chest pain, which increased new patient enrollment by 80%
  • I have a vast knowledge of several therapeutic clinical trials, development, and negotiation
  • I have been involved with monitoring of trials on the phase 1, 2, 3 clinical trials and providing assistance with the review of clinical trial-related invoices.
  • Gathered, arranged, and corrected research data to create representative graphs and charts highlighting results for presentations.
  • Helped team meet regulatory requirements by coordinating documentation and filings.
  • Distilled large amounts of information and produced reports, spreadsheets and documents outlining key details.
  • Validated incoming data to check information accuracy and integrity while independently locating and correcting concerns.
  • Gathered and organized information for research purposes.
  • Performed research into study topics to increase knowledge and to provide valuable contributions.
  • Interpreted data analysis results to draw inferences and conclusions.
  • Developed research proposals, identified research objectives and created research plans.
  • Collaborated with leadership team to identify relevant questions and determine best methods of collection.
  • Developed data collection strategies and monitored data quality for optimal research results.
  • Analyzed and interpreted patterns and trends.
  • Synthesized data and wrote detailed reports to present research findings to stakeholders.
  • Determined areas of research to increase knowledge in particular field.
  • Sorted data into well-organized formats and transformed into figures.
  • Utilized statistical packages to analyze data and create visualizations.
  • Requested or acquired equipment or supplies necessary for projects.
  • Proposed innovative methods for capturing and analyzing customer data.
  • Participated in lab meetings and project presentations.
  • Assisted scientists by collecting and organizing laboratory data.
  • Cooperated with other technicians to develop and test new protocols.
  • Set and oversaw quality assurance guidelines for laboratory work.
  • Kept abreast of current industry, scientific and regulatory developments and issues.

Clinical Research Associate II

Emzor Pharmaceutical Industries Ltd
05.2014 - 03.2017
  • I possess a good clinical practice & some experience in international conferences on Harmonization/optimization of electronic TMF (eTMF)
  • Promoted awareness of project-specific quality and performance standards to support documentation, communication and understanding.
  • Reviewed participant eligibility and consent documentation to help researchers achieve accurate and meaningful results.
  • Collected, evaluated, and modeled collected data.
  • Monitored unit budget to meet financial objectives for spend rate and funding.
  • I have a good knowledge of computer usage in using Microsoft Word/PowerPoint and the ability to use devices when needed
  • I oversaw the execution & implementation of detailed project plans in line with the stakeholders and sponsors
  • I have worked within the confines of time to maximize time management and addressed the TMF compliances in relation to data integrity
  • I oversaw protocol evaluation and regulatory compliance allowing me to focus on its accuracy
  • I have strong analytical and possess skills in the application of critical thinking skills driving good decision-making
  • I displayed strong planning/organization skills, meeting up with the work deadlines promptly
  • I ensured maximum adequate drafting and real-time reports uploading to the OCSO share point access site
  • I provide operational support to Contracting Officers' Representatives for Isolation-supported contracts and deliver clinical trial monitoring services
  • I adhere to strict adherence and advice on clinical research operations
  • I was involved with other team workers in developing protocol-specific monitoring plans tailored to the trial phases' specific human subject protection and data integrity risks
  • I possess excellent interpersonal/communication skills allowing me to collaborate with stakeholders internally and externally
  • I possess an in-depth knowledge of biologic products with an understanding of quality assurance.
  • Reviewed clinical data, source documentation, case report forms and investigative site regulatory files to verify accuracy and completion.
  • Adhered to procedures, practices and regulatory requirements to maintain health, safety and environmental compliance.
  • Conducted initiation, monitoring and closeout visits to verify study procedures, regulatory documents and data completion.
  • Collaborated with clinical study site and sponsor to troubleshoot and provide solutions to study-related issues.
  • Reviewed data queries and listings and worked with study centers to resolve data discrepancies.
  • Implemented electronic data capturing systems to adhere with clinical research guidelines.
  • Supported development and delivery of department training to maximize success of clinical research.
  • Conducted clinical trial in accordance with protocol and recorded and monitored progress.
  • Interfaced with clinical investigators and site staff to foster ethical research consistent with research plans.
  • Liaised with clinical investigator to identify, assess and resolve site performance, quality and compliance issues.
  • Maintained site monitoring schedules to facilitate effective communication with members of clinical team.
  • Facilitated quality of clinical trials by establishing project schedules and monitoring support to encourage accuracy and efficiency.
  • Observed clinical studies and assessed health outcomes in groups of participants to support research plan.
  • Mentored team members by sharing suggestions and encouraging ideas to deliver successful studies.
  • Liaised with clinical project leader to effectively resolve study-related issues.
  • Monitored safety of human subjects and oversaw consent procedures to comply with local and federal regulations.
  • Conducted meetings with sponsor representatives to discuss clinical study developments.
  • Assisted in investigator selection and qualification process to provide capable investigators with adequate resources to properly conduct trials.
  • Followed informed consent processes and maintained records.
  • Maintained compliance with protocols covering patient care and clinical trial operations.
  • Gathered, processed, and shipped lab specimens.
  • Participated in initiation visits and investigator meetings, implementing trials in accordance with study timelines and budgets.
  • Collected data and followed research protocols, operations manuals, and case report form requirements.
  • Screened patient records, databases, and physician referrals to identify prospective candidates for research studies.
  • Provided clinicians with data to conduct clinical trials and determine methods to prevent, screen for, diagnose and treat disease.
  • Established drug trial methodologies and procedures to support business and clinical trial endeavors.
  • Organized and maintained research study regulatory documents in site binder to maintain accuracy and integrity.
  • Created and maintained database and records filing system to document data on specimen collection, processing and storage.
  • Worked with principal investigator and sponsors to facilitate daily trial activities and comply with research protocols.
  • Processed specimens for clinical trials, sample storage and assay to provide registry of samples for test development, validation and analysis.
  • Gathered and organized clinical trial documentation to meet rigorous standards for site approval.
  • Coordinated and scheduled protocol-related visits and required testing to demonstrate vigilance in patient safety, protocol compliance and data quality.
  • Followed drug storage procedures to comply with protocols and SOP requirements.
  • Oversaw project developments to provide quality deliverables while maintaining optimal efficiency.
  • Traveled to investigative sites to conduct site qualification, initiation, interim monitoring and close-out visits to maintain and enforce regulatory compliance.

Education

MPH in Epidemiology -

Purdue-West Lafayette
02.2024

Bachelor's degree MBBS in Medicine -

Igbinedion University
02.2014

Skills

  • Research
  • Clinical Development
  • Patient Monitoring
  • Medical Terminology
  • FDA regulations
  • Supervisory Skills
  • Clinical Trials
  • Clinical Trial Management System (CTMS)
  • Good Clinical Practice (GCP)
  • Data Analysis
  • Clinical Research
  • Presentation Skills
  • Analysis Skills
  • Recruiting
  • GLP
  • Research & Development
  • Data Collection
  • CGMP
  • Databases
  • Data analytics (2 years)
  • Trial Master File (3 years)
  • Regulatory reporting and compliance (3 years)
  • Communication/Strong Interpersonal skills, fostering effective teamwork (4 years)

Accomplishments

  • Used Microsoft Excel to develop inventory tracking spreadsheets.
  • Supervised team of 4 staff members.

Certification

  • CCRP, 04/2023, 04/2033
  • CMT, 07/2022, 07/2024
  • RBT, 03/2020, 08/2023
  • CPR & First Aid, 02/2021, 06/2024

soccer and medicine.

I play soccer, i am an a soccer enthusiast, i got involved with soccer at a young age, i play soccer to keep my body healthy fit and strong, which i still do till this moment.

I am a fan of health, and been in this field for so long as a physician keeps me abreast and updated on my current position as a clinical care coordinator and seeing myself having to involve taking up responsibilities naturally.

Timeline

Clinical Care Coordinator

Essen Medical Associates P.C
08.2023 - Current

Sr Certified Research Associate

Southern Biotech
04.2018 - 09.2022

Clinical Research Associate II

Emzor Pharmaceutical Industries Ltd
05.2014 - 03.2017

MPH in Epidemiology -

Purdue-West Lafayette

Bachelor's degree MBBS in Medicine -

Igbinedion University

Work Availability

monday
tuesday
wednesday
thursday
friday
saturday
sunday
morning
afternoon
evening
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Work Preference

Work Type

Full Time

Work Location

HybridRemote

Important To Me

Career advancementWork-life balanceWork from home optionPersonal development programs

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FRANKLIN IBADINMD