mokolojoy
About Me
I am an adept Clinical Data Manager with 3 years of experience, aspiring to transition into Product Management. Throughout my career, I’ve successfully contributed to the initiation, execution, and oversight of clinical trial studies across 3 startups. My proficiency lies in project planning, project leadership, and effective collaboration within cross-functional teams. I am skilled in utilizing diverse tools to enhance trial database integrity, analyze trends, and address discrepancies.
My internship at SideHustle equipped me with practical expertise in product requirement documentation, user research, and market analysis, which are essential attributes for a successful Product Manager. I am eager to apply my diverse expertise as a data and product manager to new industries beyond healthcare. My goal as a Product Manager is to drive innovation by creating customer-centric products that yield substantial revenue.
Education
Babcock University
Graduated with a First Class Degree CGPA: 4.73/ 5.0
Bowen University
Graduated with a Second Class (Upper Division) CGPA: 4.03/ 5.0
Work & Experience
Freelance Facilitator/Clinical Data Manager
NK Clinicals
● Mentored and trained team members in all aspects of clinical data management, resulting in a notable 90% increase in employee efficiency during daily operations. ● Undertakes ad-hoc, high-level tasks and delivers supervisory support to junior team members, fostering a collaborative and efficient work environment.
Lead Clinical Data Manager
Zilla Clinicals
● Spearheaded company growth initiatives by actively contributing to operational strategies aimed at increasing revenue and expanding the company's presence. ● Established a training and mentorship program for interns and external trainees, resulting in a remarkable 55% boost in company revenue. ● Successfully oversaw and coordinated numerous clinical trial projects and deliverables, while acting as the primary liaison for cross-functional team collaboration. ● Managed direct reports, ensuring the achievement of key performance indicators (KPIs) and maintaining a high standard for project execution, maintenance, and completion. ● Drafted specifications for database build and collaborated closely with developers to execute the features outlined in the specification documents. ● Performed User Acceptance Testing (UAT) of study databases, encompassing validation of data entry interfaces, edit checks, and other functionalities during database build and post-production migration. ● Conducted Vendor Reconciliation of Serious Adverse Events (SAEs), Central Laboratory Data, ECGs, and Imaging data using Microsoft Excel to ensure accuracy. ● Authored essential clinical data management documents, including electronic Case Report Forms (eCRF), Data Management Plan (DMP), eCRF Completion Guidelines (CCG), Data Validation Specification (DVS), and Data Transfer Specifications (DTS) using Microsoft Word. ● Reviewed clinical trial data on an ongoing basis to ensure quality data and performed query management for the resolution of identified discrepancies. ● Monitored and visualized study data for the identification of issues and trends using Medidata 360 reports, Tableau, PowerBI, and created custom reports using IBM Cognos, J-Review and Business Objects
Senior Clinical Data Specialist I
Clinfocus Inc
● Led cross-functional teams in end-to-end clinical data management activities, from project launch to database lock. ● Trained junior team members for increased efficiency and collaboration. ● Developed SOPs aligning data management with business priorities and compliance. ● Proactively anticipated issues and addressed data challenges with metrics-driven solutions. ● Managed user access to ensure data security and integrity across various Clinical Data Management Systems. ● Created timelines using MS Project and SmartSheet for key project milestones. ● Conducted third-party vendor data reconciliation (Serious Adverse Events, Pharmacokinetics, Pharmacodynamics, Central Laboratory, and Imaging data). ● Performed User Acceptance Testing (UAT) for databases during and after Go-Live. ● Designed CDISC-aligned Case Report Forms, enhancing data collection efficacy. ● Created and updated essential data management documents and maintained study metrics reports. ● Reviewed and managed study data, queries, and reports in various EDC Systems, including Medidata Rave, Medrio, Oracle Clinical One, IBM Clinicals, DataTrak, Calyx/DataLab.
Product Management Intern
SideHustle
• Collaborated with design and engineering teams to ensure the successful implementation and timely delivery of product features and functionalities. • Conducted user surveys and competitive analysis to inform product development decisions. • Developed user personas, stories, scenarios, and acceptance criteria to guide the product development process. • Utilized Jira and Whimsical to create product roadmaps for sprint planning, monitored the progress of cross-functional teams through daily standup meetings, and conducted sprint reviews at the end of each sprint to evaluate accomplishments and gather feedback. • Created comprehensive product requirements document that outlined the product overview, problem statement, competitive analysis report, success metrics, user flow, and other product information. • Created wireframes using Miro, Figma and FigJam to visually illustrate and communicate product ideas.
