Mercedes C. Morales Castro

• Coordinated clinical trial activities, ensuring compliance with regulatory guidelines and protocols.
• Assisted in patient recruitment and informed consent processes to enhance study participation.
• Managed data collection and documentation using electronic data capture systems for accuracy.
• Collaborated with multidisciplinary teams to facilitate communication between departments and stakeholders.
• Trained new team members on essential clinical research protocols and procedures, promoting a culture of continuous learning.
• Screened patient records, databases, and physician referrals to identify prospective candidates for research studies.
• Gathered, processed, and shipped lab specimens.
• Worked with principal investigator and sponsors to facilitate daily trial activities and comply with research protocols.
• Assessed patients'' eligibility criteria following strict adherence to inclusion/exclusion guidelines.
• Streamlined process for serious adverse event reporting, enhancing safety monitoring efforts.

• Coordinated clinical trial activities, ensuring compliance with regulatory standards and protocols.
• Developed and maintained study documentation, enhancing data accuracy and integrity.
• Managed patient recruitment strategies, optimizing enrollment timelines for clinical studies.
• Collaborated with cross-functional teams to streamline research processes and improve operational efficiency.
• Trained junior staff on best practices in clinical research methodologies and data management systems.
• Oversaw budget management for multiple clinical trials, ensuring optimal resource allocation and cost control.
• Facilitated communication between investigators, sponsors, and regulatory bodies to ensure project alignment and timely execution.
• Accelerated study completion by effectively managing clinical trial schedules and coordinating site visits.
• Maximized protocol compliance by providing comprehensive training to research staff and ensuring adherence to guidelines.
• 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.
• Worked with principal investigator and sponsors to facilitate daily trial activities and comply with research protocols.
• Gathered, processed, and shipped lab specimens.
• Screened patient records, databases, and physician referrals to identify prospective candidates for research studies.
• Ensured timely and accurate completion of case report forms (CRFs) and data entry across different electronic data capture (EDC) systems.

Clinical Research Coordinator

• Coordinated patient recruitment and retention strategies for clinical trials.
• Developed study materials and ensured adherence to Good Clinical Practice guidelines.
• Gathered, processed, and shipped lab specimens.
• Assessed patients'' eligibility criteria following strict adherence to inclusion/exclusion guidelines.
• Conducted the informed consent process and coordinated participant visits, and procedures.

Physician Liaison

• Cultivated relationships with healthcare providers to enhance referral networks.
• Provided support for clinical staff through regular communication and educational initiatives.
• Collaborated with marketing teams to develop effective outreach strategies for physician engagement.
• Served as a liaison between patients, families, and medical professionals, ensuring seamless coordination of care throughout treatment processes.

• Assisted the surgeon during minimally invasive Vascular procedures.
• Maintained sterile environments and adhered to safety protocols throughout surgical processes.
• Kept views unobstructed by retracting, sponging, and suctioning surgical sites.
• Collaborated with the surgical team to enhance workflow efficiency and patient care standards.
• Prepared and handled surgical instruments, ensuring availability and functionality for each procedure.
• Educated patients on pre-operative instructions, contributing to improved compliance and satisfaction rates.
• Mentored junior staff in surgical techniques and best practices, fostering a knowledgeable team environment.
• Increased patient satisfaction through compassionate pre-and post-operative communication and care.
• Assessed patients'' vitals before surgery to ensure stable condition throughout the procedure.

• Diagnosed and treated diverse medical conditions, ensuring optimal patient care standards.
• Collaborated with multidisciplinary teams to develop and implement comprehensive treatment plans.
• Conducted physical examinations and diagnostic tests to accurately diagnose patients'' medical conditions.
• Mentored junior physicians and medical interns, fostering professional development and clinical skills enhancement.
• Advocated for preventative care measures within the community to promote health awareness and education.
• Collaborated with specialists for comprehensive patient care, resulting in improved health outcomes.
• Provided ongoing support to patients with chronic illnesses by monitoring their progress and adjusting treatment plans as necessary.
• Participated in continuing education programs to stay current on the latest advancements in medical knowledge and technology.
• Educated patients on disease prevention and healthy lifestyle choices, contributing to overall community wellbeing.
• Prescribed or administered treatment, therapy and medication to treat or prevent illness, disease or injury.
• Conferred with specialists to obtain expertise on patient conditions and referred individuals in need of additional care.

Regional Project Manager for the Centers for Disease Control & Prevention (03/2012 - 11/2013)

• Monitored data collection processes for accuracy and adherence to protocols.
• Provided training and support to junior team members on project-related tasks.
• Enhanced patient recruitment for clinical studies by developing targeted marketing materials and outreach strategies.
• Ensured data integrity in clinical trials by implementing rigorous quality control measures and closely monitoring study progress.