Work History
Overview
Education
Skills
Summary
Certification
RegisteredNurse
Jenine Dennis

Jenine Dennis

Clinical Research Coordinator
Krum,TX

Work History

Per Diem Remote Clinical Research Recruiter/remote

NeuroCare
Newton, MA
2024.04 - Current
  • Excellent communication skills, both verbal and written.
  • Worked flexible hours across night, weekend, and holiday shifts.
  • Managed time efficiently in order to complete all tasks within deadlines.
  • Organized and detail-oriented with a strong work ethic.
  • Strengthened communication skills through regular interactions with others.
  • Learned and adapted quickly to new technology and software applications.
  • Developed and maintained courteous and effective working relationships.
  • Demonstrated strong organizational and time management skills while managing multiple projects.

Clinical Research Coordinator ,remote, contract

Science 37
Culver City , CA
08.2023 - 01.2024
  • 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.
  • 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.
  • Coordinated and monitored clinical trial activities to support timely and accurate completion of studies.
  • Worked with principal investigator and sponsors to facilitate daily trial activities and comply with research protocols.
  • Trained new team members on essential clinical research protocols and procedures, promoting a culture of continuous learning.
  • Managed patient recruitment, informed consent process and data entry to support trial objectives.
  • Prepared and maintained regulatory documents for clinical trial submissions.
  • Reduced data entry errors by implementing stringent quality control measures throughout the study lifecycle.

Senior Clinical Research Coordinator

Dermatology Treatment and Research Center
Dallas, TX
01.2023 - 08.2023
  • Contributed to the successful completion of numerous studies by coordinating all aspects of trial initiation, execution, and close-out activities.
  • Collaborated with investigators to develop innovative clinical trial designs, optimizing data collection methods for better results.
  • Ensured compliance with regulatory requirements by conducting thorough audits of study documents and procedures.
  • Developed robust data management plans for efficient data capture, analysis, and reporting throughout the study lifecycle.
  • Optimized patient safety during clinical trials by diligently monitoring adverse events and promptly escalating concerns when necessary.
  • Enhanced data quality by closely monitoring study metrics and resolving discrepancies in a timely manner.
  • Served as a liaison between site personnel, investigators, and sponsors to ensure clear communication throughout the trial process.
  • Fostered a positive working environment for research staff through regular team-building activities and ongoing professional development opportunities.
  • Reduced protocol deviations by providing comprehensive training and support to research staff.
  • Facilitated clinical trial progression, effectively managing multiple projects simultaneously.
  • Improved patient recruitment by developing and implementing targeted outreach strategies.
  • Increased patient retention rates by establishing strong relationships with participants through effective communication and followup.
  • Followed clinical research protocols and conducted study visits in compliance with ICH/GCP and FDA regulations.
  • 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.
  • Screened patient records, databases, and physician referrals to identify prospective candidates for research studies.
  • Followed informed consent processes and maintained records.
  • Gathered, processed, and shipped lab specimens.
  • Managed patient recruitment, informed consent process and data entry to support trial objectives.
  • Participated in initiation visits and investigator meetings, implementing trials following study timelines and budgets.
  • Collected data and followed research protocols, operations manuals, and case report form requirements.
  • Monitored patient safety throughout clinical trials and reported any adverse events.
  • Maintained accurate and up-to-date case report forms and source documents for traceability.
  • Developed and maintained accurate and up-to-date case report forms and source documents.
  • Prepared and maintained regulatory documents for clinical trial submissions.
  • Complied with research protocols by providing ongoing quality control audits.
  • Reviewed referral information and kept track of intakes from various referral sources.
  • Collected, evaluated, and modeled collected data.

Senior Clinical Research Coordinator, remote

Vault Health
Coral Gables, FL
06.2022 - 10.2022
  • Developed robust data management plans for efficient data capture, analysis, and reporting throughout the study lifecycle.
  • Streamlined study processes for increased efficiency by collaborating with cross-functional teams on protocol development and implementation.
  • Collaborated with investigators to develop innovative clinical trial designs, optimizing data collection methods for better results.
  • Fostered a positive working environment for research staff through regular team-building activities and ongoing professional development opportunities.
  • Implemented quality control measures across all areas of the study process to ensure accurate, reliable data collection and analysis.
  • Reduced protocol deviations by providing comprehensive training and support to research staff.
  • Coordinated with other departments such as biostatistics and regulatory affairs to streamline processes and ensure successful project completion.
  • Served as a liaison between site personnel, investigators, and sponsors to ensure clear communication throughout the trial process.
  • Optimized patient safety during clinical trials by diligently monitoring adverse events and promptly escalating concerns when necessary.
  • Increased patient retention rates by establishing strong relationships with participants through effective communication and followup.
  • Contributed to improved patient outcomes by providing valuable input on the development of new clinical trial protocols and methodologies.

Clinical Research Coordinator

National Allergy and Ent
North Charleston, SC
04.2014 - 06.2022
  • Followed clinical research protocols and conducted study visits in compliance with ICH/GCP and FDA regulations.
  • Collected, evaluated, and modeled collected data.
  • Developed strong relationships with trial sponsors, ensuring ongoing collaboration and future project opportunities.
  • Maintained compliance with regulatory guidelines through rigorous documentation and protocol adherence.
  • Contributed to the successful completion of clinical trials by proactively resolving issues, mitigating risks, and meeting deadlines in a fast-paced environment.
  • Followed informed consent processes and maintained records.
  • 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.
  • Reduced data entry errors by implementing stringent quality control measures throughout the study lifecycle.
  • Coordinated with cross-functional teams to ensure timely completion of clinical trial milestones.
  • Prepared and maintained regulatory documents for clinical trial submissions.
  • Prepared detailed informed consent documents to clearly communicate risks, benefits, expectations, rights and responsibilities related to participation in clinical trials.
  • Gathered, processed, and shipped lab specimens.
  • Enhanced patient safety by meticulously monitoring and documenting adverse events during clinical trials.
  • Oversaw the management of investigational product supplies, ensuring appropriate storage conditions were maintained at all times for optimal efficacy during trials.
  • Managed patient recruitment, informed consent process and data entry to support trial objectives.
  • Complied with research protocols by providing ongoing quality control audits.
  • Participated in initiation visits and investigator meetings, implementing trials following study timelines and budgets.
  • Trained new team members on essential clinical research protocols and procedures, promoting a culture of continuous learning.
  • Developed and maintained accurate and up-to-date case report forms and source documents.
  • Directed site initiation visits, establishing key partnerships with local healthcare providers to facilitate successful trial implementation.

Certified Medical Assistant

National Allergy & Asthma (ENT)
North Charleston, SC
04.2010 - 04.2014
  • Sanitized, restocked, and organized exam rooms and medical equipment.
  • Directed patients to exam rooms, fielded questions, and prepared for physician examinations.
  • Called and faxed pharmacies to submit prescriptions and refills.
  • Provided compassionate care for patients, addressing their concerns and ensuring a positive experience.
  • Documented vital signs and health history for patients in clinic and hospital environments.
  • Assisted physicians with various procedures, ensuring comfort and accuracy for optimal patient outcomes.
  • Collected and documented patient medical information such as blood pressure and weight.
  • Reduced wait times for patients by maintaining an organized schedule and swiftly preparing examination rooms.
  • Assisted with routine checks and diagnostic testing by collecting and processing specimens.
  • Kept medical supplies in sufficient stock by monitoring levels and submitting replenishment orders before depleted.
  • Enhanced clinic efficiency by thoroughly documenting patient information and updating electronic health records.
  • Taught patients about medications, procedures, and care plan instructions.
  • Prepared and administered medications to alleviate patient symptoms.
  • Increased patient safety by meticulously following infection control protocols and maintaining a sterile environment.
  • Consistently maintained up-to-date certifications, demonstrating dedication to professional development and quality patient care.
  • Educated patients on preventative care measures, effectively reducing the risk of future health complications.
  • Performed medical records management, including filing, organizing and scanning documents.
  • Prepared lab specimens for diagnostic evaluation.
  • Oriented and trained new staff on proper procedures and policies.
  • Measured patient spirometry.

Overview

14
14
years of professional experience
2
2
years of post-secondary education

Education

Associate of Applied Science - Medical Assistang

Miller-Motte Technical College, Charleston,SC
North Charleston, SC
04.2008 - 04.2010

Skills

  • Regulatory Requirements
  • Study Coordination
  • Medication Dispensing
  • Reading Comprehension
  • Investigator Meetings
  • Computerized Maintenance Management Systems
  • Documentation Requirements
  • Patient Safety
  • Lab Specimens and Collections
  • Case Report Management
  • Team Meetings
  • Documentation Management
  • Informed Consent
  • Participant Recruitment
  • Creative Thinking
  • Records Maintenance
  • Monitoring Visits
  • Research Sops Understanding
  • Scheduling Proficiency
  • Study Protocols
  • Investigator Coordination
  • Trial Oversight
  • Medical Histories and Vital Statistics
  • Data Analysis
  • Site Visits
  • Site Preparation
  • Facility Management
  • Enrollment Oversight
  • Adverse Event Documentation
  • Medidata Rave
  • Good Clinical Practice
  • Phlebotomy
  • Prospective Studies

Summary

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. Organized and dependable candidate successful at managing multiple priorities with a positive attitude. Willingness to take on added responsibilities to meet team goals. Detail-oriented team player with strong organizational skills. Ability to handle multiple projects simultaneously with a high degree of accuracy. My purpose is to seek and maintain full-time position that offers professional challenges utilizing interpersonal skills, excellent time management and problem-solving skills.

Certification

  • GCP Certificate, CITI -29 Aug-2023-2026
  • IATA issued 2023

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Jenine DennisClinical Research Coordinator