Rosibel Martinez

• Participated in initiation visits and investigator meetings, implementing trials in accordance with study timelines
• Gathered, processed and shipped lab specimens
• Collected data and followed research protocols, operations manuals and case report form requirements
• Coordinated clinical trials focused on disorders such as Diabetes Cholesterol Hypertension Rheumatoid Arthritis Osteoarthritis Flu Contraceptive Lupus Kidney Disease ] and Anemia
• Followed informed consent processes and maintained records
• Worked with principal investigator and sponsors to facilitate daily trial activities and ensure compliance with research protocols
• Screened patient records, databases and physician referrals to identify prospective candidates for research studies
• Maintained compliance with protocols covering patient care and clinical trial operations
• Interviewed patients to obtain medical information, weight and height measurements and vital signs

Participated in initiation visits and investigator meetings, implementing trials in accordance with study timelines
Gathered, processed and shipped lab specimens
Collected data and followed research protocols, operations manuals and case report form requirements
Coordinated clinical trials focused on disorders such as Diabetes Cholesterol Hypertension Rheumatoid Arthritis Osteoarthritis Flu Contraceptive Lupus Kidney Disease ] and Anemia
Followed informed consent processes and maintained records
Worked with principal investigator and sponsors to facilitate daily trial activities and ensure compliance with research protocols
Screened patient records, databases and physician referrals to identify prospective candidates for research studies
Maintained compliance with protocols covering patient care and clinical trial operations
Interviewed patients to obtain medical information, weight and height measurements and vital signs

Participated in initiation visits and investigator meetings, implementing trials in accordance with study timelines
Gathered, processed and shipped lab specimens
Collected data and followed research protocols, operations manuals and case report form requirements
Coordinated clinical trials focused on disorders such as Diabetes Cholesterol Hypertension Rheumatoid Arthritis Osteoarthritis Flu Contraceptive Lupus Kidney Disease ] and Anemia
Followed informed consent processes and maintained records
Worked with principal investigator and sponsors to facilitate daily trial activities and ensure compliance with research protocols
Screened patient records, databases and physician referrals to identify prospective candidates for research studies
Maintained compliance with protocols covering patient care and clinical trial operations
Interviewed patients to obtain medical information, weight and height measurements and vital signs