Jodian Palmer
Chase Medical Research, LLC
1
Certification
10
years of professional experience
Professional with experience in clinical research coordination, equipped to make significant impact in this field. Demonstrated 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 results-driven approach that ensures successful study outcomes.
Results-driven research professional prepared for challenges of overseeing clinical studies. Proven track record of managing complex projects and ensuring compliance with research protocols. Known for fostering team collaboration and adapting to evolving project needs, while excelling in data management and regulatory adherence.
Diligent Clinical Research Project Coordinator with comprehensive background in coordinating clinical research studies. Successfully managed multiple clinical trials from initiation to closeout, ensuring adherence to regulatory guidelines. Demonstrated ability to effectively communicate with cross-functional teams and maintain meticulous documentation.
Organized and dependable candidate successful at managing multiple priorities with a positive attitude. Willingness to take on added responsibilities to meet team goals.
Work History
Clinical Research Coordinator Assistant Supervisor
1 Year 10 Months- Company Overview: www.chasemr.com
- Followed clinical research protocols and conducted study visits in compliance with ICH/GCP and FDA regulations.
- 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.
- 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.
- Gathered, processed, and shipped lab specimens.
- Maintained accurate and up-to-date case report forms and source documents for traceability.
- Coordinated clinical trial activities, ensuring compliance with regulatory standards and protocols.
- Managed participant recruitment and retention strategies, enhancing study enrollment efficiency.
- Oversaw site visits and monitoring activities, ensuring adherence to Good Clinical Practice guidelines.
- Trained and mentored junior staff on clinical trial procedures and best practices.
- Led initiatives to optimize workflow efficiencies, reducing project timelines while maintaining quality standards.
- Followed informed consent processes and maintained records.
- Enhanced patient safety by meticulously monitoring and documenting adverse events during clinical trials.
- Collaborated with clinical staff and other healthcare professionals to support clinical trial data accuracy.
Lead Laboratory Assistant
2 Years 5 Months- Supervised daily laboratory operations, ensuring compliance with safety protocols and procedures.
- Trained and mentored junior laboratory staff on best practices and equipment usage.
- Developed and implemented standard operating procedures to improve workflow efficiency.
- Conducted quality control tests to maintain accuracy in experimental results and data integrity.
- Collaborated with cross-functional teams to support research initiatives and project goals.
- Analyzed data trends, providing insights that informed strategic decisions in experimental design.
- Coordinated with other departments within the organization for seamless collaboration on cross-functional projects or initiatives.
- Maintained laboratory equipment in optimal working condition through regular calibration, cleaning, and troubleshooting efforts.
- Enhanced laboratory efficiency by streamlining sample processing and implementing effective organizational systems.
Certified Phlebotomist
4 Years 9 Months- Performed venipuncture and capillary draws with precision and care, ensuring patient comfort.
- Maintained accurate records of specimen collection, adhering to hospital protocols and standards.
- Trained and mentored new staff on best practices in blood collection techniques and safety measures.
- Implemented quality control measures to enhance specimen integrity and reduce errors in processing.
- Protected patients by following infection control, sharps disposal, and biohazardous waste disposal procedures.
- Contributed to positive patient experiences through empathetic communication skills during blood draws and sample collections.
Education
Licensed Practical Nurse Program - LPN
Phlebotomy Certificate
General Studies
Skills
Good clinical practices
Clinical trial management
Clinical research ethics
Adverse event reporting
Data collection techniques
Phlebotomy
Specimen collections
Specimen handling
Certification
- iMedidata
- Veeva Vault
- Zelta
- CITI Collaborative Institutional Training Initiative
- HIPAA Training for Research
- Clinical Research IO (CRIO) Certification
- Society for Clinical Research Sites Certification
- IATA Certified in the Transportation of Dangerous Goods by Air
Timeline
Clinical Research Coordinator Assistant Supervisor
Chase Medical Research, LLC
09.2024 - CurrentRead More
Lead Laboratory Assistant
Hartford Hospital
04.2022 - 09.2024Read More
Certified Phlebotomist
St. Mary’s Hospital
10.2016 - 07.2021Read More
Academy of Medical Training
Phlebotomy Certificate
Read More
Lincoln Technical Institute
Licensed Practical Nurse Program from LPN
Read More
Albertus Magnus College
General Studies
Read More
Research
- Long-term effects of (study drug) on diabetic retinopathy in subjects with type 2 diabetes.
- The Effect of (study drug) on Major Adverse Cardiovascular Events in Patients with Type 2 Diabetes
- Safety and Immunogenicity Study of (study drug) Vaccine Candidate Against Lyme Borreliosis: A Randomized, Controlled, Observer-Blind Phase 2 Study in a Healthy Pediatric and Adult Study Population
- A Phase 3 Randomized, Observer-Blind, Study to Evaluate Safety, Tolerability, and Immunogenicity of (study drug) Vaccine Targeting Respiratory Syncytial Virus (RSV), When Given Alone or Coadministered.
- A randomized double-blind, placebo-controlled, multicenter trial assessing the impact of lipoprotein (a) lowering with (study drug) on major cardiovascular events in patients with established cardiovascular disease
- A randomized, double-blind, placebo-controlled, multicenter trial, assessing the impact of (study drug) on major adverse cardiovascular events in participants with established cardiovascular disease.
- A Post Approval Study to Evaluate the Safety of the Eversense Continuous Glucose Monitoring (CGM) System Used Non-adjunctively
- A Phase 3, Randomized, Double-Blind, Placebo-Controlled Study to Investigate the Effect of (study drug) on the Reduction of Morbidity and Mortality in Adults with Obesity
- A Phase 3, randomised, double-blind, parallel-group, event-driven, cardiovascular safety study with (study drug) administered subcutaneously compared with placebo in participants with overweight or obesity with established cardiovascular disease (CVD) or chronic kidney disease, and/or at least two weight-related complications or risk factors for CVD
- A Phase 3 Randomized, Placebo-Controlled Clinical Study to Evaluate the Efficacy and Safety of (study drug) in Reducing Major Adverse Cardiovascular Events in Participants at High Cardiovascular Risk.
Signature
Jodian Palmer