Keep in touch with meI'm using Intch to connect with new people. Use this link to open chat with me via Intch app
Work Background
IQVIASenior Clinical Research Associate
Jun. 2024South Africa• Perform site selection, initiation, interim monitoring, close out etc.
* Assist site to build quality systems
* Sponsor Audit and Regulatory Inspection preparation and post CAPA development
IQVIAClinical Research Associate II
Nov. 2023 - Jun. 2024Ghana• Perform site selection, initiation, interim monitoring, close out etc.
* Assist site to build quality systems
* Sponsor Audit and Regulatory Inspection preparation and post CAPA development
IQVIAClinical Research Associate 2 - Novartis cFSP CRA
Mar. 2022 - Oct. 2023Accra, Greater Accra, Ghana• Perform site selection, initiation, interim monitoring, close out etc.
* Assist site to build quality systems
* Sponsor Audit and Regulatory Inspection preparation and post CAPA development
IQVIAClinical Research Associate 1
Aug. 2020 - Feb. 2022Accra, Greater Accra, Ghana• Perform site selection, initiation, interim monitoring, close out etc.
* Assist site to build quality systems
* Sponsor Audit and Regulatory Inspection preparation and post CAPA development
IQVIAAssociate CRA
Aug. 2019 - Jul. 2020Accra, Greater Accra, Ghana• Perform site selection, initiation, monitoring and close-out visits in accordance with contracted scope of work and good clinical practice.
• Provide monitoring visits and site management for a variety of protocols, sites and therapeutic areas.
• Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues.
• Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues to Clinical Team Lead (CTL) and/or line manager.
• Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment case report form (CRF) completion and submission, and data query generation and resolution.
• Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports and other required study documentation.
• May provide assistance to more or less experienced clinical staff.
KHRCResearch Fellow
- May. 2022
Intch is a Professional Networking App for the Future of WorkSee more people like Philip on Intch
300k+ people
130+ countries
AI matching
Get Intch if you'd like to
1086233 people
38
Graphic Designer @ Tanya Design
15
Marketing Director @ The Delaware State Fair, Inc.
17
Creative Lead @ Mischievous Creative Studio
206362 people
17
Product Designer @ SUPERSMAIL GmbH
15
UX & Strategy Designer
17
Creative Art Director/ Full-stack Marketing Manager @ Ninabelle Tukha Creative