Edward Mould

• Developed 20+ KOL relationships, improving engagement rates by 35%.
• Collaborated on 10 clinical trial protocols, enhancing alignment across cross-functional teams.
• Delivered 25+ presentations on research findings to healthcare providers.
• Assisted in preparing comprehensive reports for internal and external stakeholders, ensuring clarity and accuracy.
• Maintained detailed records of all interactions with customers and clients, supporting effective communication and follow-up.
• Developed and maintained effective relationships with internal and external stakeholders.
• Identified opportunities for improvement in processes and procedures related to liaison activities.

• Assisted in filling prescriptions accurately and efficiently for diverse patient needs.
• Collaborated with healthcare professionals to ensure optimal patient care delivery.
• Supported pharmacy operations by processing insurance claims and payments diligently.
• Advised customers on over-the-counter medications and health products confidently.
• Ensured compliance with safety protocols and best practices in medication handling.
• Counseled customers on the proper use of over-the-counter medications.
• Reviewed and verified patient information for accuracy and completeness prior to dispensing medication.

Performed all types of site visits during the life cycle of assigned clinical research projects
(PSSV, SIV, IMV and COV).
● Conducted assigned site initiation visits, to include training of site personnel on Sponsor
and regulatory requirements for study conduct
● Monitored investigative clinical sites through regular interim monitoring visits according to
sponsor clinical monitoring plans with visit windows.
● Ensured strict adherence to protocol and applicable regulatory requirements via 100%
source document verification of source data with vendor electronic data capture
systems/eCRFs.
● Continuously maintained Investigator Site Files by ensuring updated essential documents
including Institutional Review Board approvals are on file.
● Monitored subject informed consent with great attention to detail for proper procedure and
instituted correction actions on identification of discrepancies.
● Confirmed eligibility of screened subjects for eligibility inclusion/exclusion criteria to ensure
appropriate randomization and screen failed subjects as applicable.
● Reviewed Adverse Events, Serious Adverse Events, and SUSARS onsite to ensure proper
reporting to Sponsor within study timelines.
● Monitor subject follow-up from 3-year clinical trial.
● Coordinate laboratory samples and compile data.
● Collaborate with medical professionals to determine changes in subjects’ conditions.
● Performed site visits to verify the suitability and viability of the investigational site for the
conduct of clinical studies in accordance with the study plan and sponsor’s SOPs
● Trained site personnel during initiation visits and managed study conduct at the site to
ensure high-level site performance.
● Performed both onsite and remote source document verification to ensure the accuracy of
data entered into the CRF/eCRF.
● Identified and tracked protocol deviations/violations along with deficiencies during
monitoring visits, and provided additional training and/or initiated corrective action as
required
● Discussed relevant visit findings with Principal Investigators via face-to-face meeting and
scheduledV

• Monitored clinical trial protocols and compliance with regulatory requirements.
• Collaborated with research teams to ensure data collection accuracy.
• Assisted in preparing documentation for regulatory submissions and audits.

• Conduct detailed medication therapy management and monitoring for patients.
  ● Collaborate with healthcare team members to develop individualized patient care plans.
  ● Provide expert consultation on medication use and safety to healthcare providers.
  ● Educate patients and their families on medication therapy, side effects, and interactions.
  ● Participate in the development and implementation of clinical protocols and guidelines.
  ● Perform comprehensive medication reviews to optimize drug therapy.
  ● Assist in the coordination of discharge planning and follow-up care.
  ● Contribute to clinical research and quality improvement projects.
  ● Prepare and present continuing education sessions for healthcare professionals.