Marshagay Rodriques
The Bronx,NY
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.
Overview
7
7
years of professional experience
Work History
Clinical Research Manager
Weill Cornell Medical Center
08.2021 - Current
- Worked with principal investigator and sponsors to facilitate daily trial activities and comply with research protocols.
- Screened patient records, databases, and physician referrals to identify prospective candidates for research studies.
- Collected data and followed research protocols, operations manuals, and case report form requirements.
- Followed informed consent processes and maintained records.
- Maintained compliance with protocols covering patient care and clinical trial operations.
- Monitored unit budget to meet financial objectives for spend rate and funding.
- Skilled at working independently and collaboratively in a team environment.
- Strengthened communication skills through regular interactions with others.
- Proved successful working within tight deadlines and a fast-paced environment.
- Collected, evaluated, and modeled collected data.
- Gathered, processed, and shipped lab specimens.
- Participated in initiation visits and investigator meetings, implementing trials in accordance with study timelines and budgets.
Lead Clinical Research Coordinator
Memorial Sloan Kettering Cancer Center, Chemotherapy Unit
03.2016 - 03.2021
- Participated in initiation visits and investigator meetings, implementing trials in accordance with study timelines and budgets.
- Gathered, processed, and shipped lab specimens.
- Screened patient records, databases, and physician referrals to identify prospective candidates for research studies.
- Followed informed consent processes and maintained records.
- Collected data and followed research protocols, operations manuals, and case report form requirements.
- Worked with principal investigator and sponsors to facilitate daily trial activities and comply with research protocols.
- Maintained compliance with protocols covering patient care and clinical trial operations.
- Skilled at working independently and collaboratively in a team environment.
- Self-motivated, with a strong sense of personal responsibility.
- Proven ability to learn quickly and adapt to new situations.
- Worked well in a team setting, providing support and guidance.
- Worked effectively in fast-paced environments.
- Managed time efficiently in order to complete all tasks within deadlines.
- Demonstrated respect, friendliness and willingness to help wherever needed.
- Excellent communication skills, both verbal and written.
- Passionate about learning and committed to continual improvement.
- Strengthened communication skills through regular interactions with others.
Education
High School Diploma -
Miami Carol City Senior High School
Miami Gardens, FLAssociate of Science - Science Education
Bronx Community College of The City University of New York
The Bronx, NY06.2018
Skills
- Site Monitoring
- Patient Information
- Protocol Development
- Trial Procedure
- Administrative Support
- Budget Controls
- Site Investigations
- Systems Analysis
- Lab Testing
- Clinical Trials and Research
- Client Assessments
- Specimen Coordination
- Trial Oversight
- Procurement Management
- Good Clinical Practice
- Experimental Protocols
- Contract Development
- Research Sops Understanding
- Workflow Management
- Complex Problem-Solving
- Laboratory Results Management
- Regulatory Documentation
- Materials Purchasing
- Regulatory Auditing
- Dispensing Oversight
- Study Management
- Regulatory Reporting
- Treatment Plans
- Case Report Management
- Drug Storage Procedures
- Monitoring Plans
- Protocol Compliance
- Site Management
- Grant Submissions
- Clinical Interventions
- Adverse Event Documentation
- Lab Specimens and Collections
- Investigator Meetings
- Medidata Rave
- Report Documentation
- Clinical Data Collection
- Compliance Reviews
- Heart Failure
- Patient Record Database Management
- Site Visits
- Statistical Analysis
- HIPAA Guidelines
- Learning Strategies
- Clinical Documentation
- Trial Close
- Stipend Distribution
- Storage Oversight
- Clinical Programming
- Visitation Scheduling
- Client Support
- Active Learning
- Client Satisfaction
- Treatment Administration
- Documentation Research
- Study Coordination
- Prospective Studies
- Team Meetings
- Participation Reviews
- Specimen Storage
- Regulatory Requirements
- Enrollment Oversight
- Patient Flow
- Database Oversight
- Pharmaceutical Research
- Informed Consent
- Master File Management
- Research Activity Tracking
- Study Monitoring
- Data Collections
- Management of Personnel Resources
- Database Design and Management
- Records Management Systems
- Clinical Monitoring
- FDA Compliance
- Database Research
- Federal Regulations
- Social Perceptiveness
- Reading Comprehension
- Investigational New Drug (IND) Processes
- Quality Improvement Plans
- Reporting Oversight
- Potential Subject Evaluation
- Product Inventories
- Study Protocols
Work Availability
monday
tuesday
wednesday
thursday
friday
saturday
sunday
morning
afternoon
evening
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Quote
There is a powerful driving force inside every human being that, once unleashed, can make any vision, dream, or desire a reality.
Tony Robbins
Timeline
Clinical Research Manager
Weill Cornell Medical Center
08.2021 - Current
Lead Clinical Research Coordinator
Memorial Sloan Kettering Cancer Center, Chemotherapy Unit
03.2016 - 03.2021
High School Diploma -
Miami Carol City Senior High School
Associate of Science - Science Education
Bronx Community College of The City University of New York
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