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The following curriculum of courses have been determined by WMDO experts to help you to reach your career objectives according to the position you have selected and are divided into sections which will allow you to follow the proposed training in an efficient and structured manner.

For this reason, we strongly recommend that you complete each section before moving along to the next.

You must be logged into your account in order to view your personal training progress in the results below.

Senior Clinical research associate

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Step 1

Course Title Click on a title to view course descriptionStatusDurationBasicPremiumPurchase
CPM: Objectives and Setup of a Medical Device Clinical TrialRecommended35 mins€ 160.00€ 120.00
CPM: The Clinical Trial master plan for Medical DevicesRecommended50 mins€ 200.00€ 150.00
CPM: Medical Device Clinical Trials - Budget and Timelines PlanningRecommended100 mins€ 400.00€ 300.00
CPM: Medical Device Clinical Trial Team ResourcesRecommended50 mins€ 200.00€ 150.00
CPM: Tracking and Reporting Rules for Medical Device Clinical TrialsRecommended25 mins€ 100.00€ 75.00
CPM: Project Guidelines for Medical Device Clinical TrialsRecommended30 mins€ 120.00€ 90.00
CPM: Managing Ongoing Medical Device Clinical TrialsRecommended20 mins€ 80.00€ 60.00
CPM: Compliance Management during Medical Device Clinical TrialsRecommended40 mins€ 160.00€ 120.00
CPM: Effective Communication Methods during Medical Device Clinical TrialsRecommended50 mins€ 200.00€ 150.00
CPM: Close Out and Clinical Report of a Medical Device Clinical TrialRecommended30 mins€ 120.00€ 90.00
ISO 14971: 2007 ReviewRecommended35 mins€ 107.00€ 80.00
Preparing Risk Management File & Which Techniques ApplyRecommended24 mins€ 73.00€ 55.00
Integrating Risk Management into Your Quality Management SystemRecommended35 mins€ 107.00€ 80.00
Effective Time ManagementRecommended176 mins€ 604.00€ 483.00
Powerful Presentation SkillsRecommended140 mins€ 267.00€ 200.00
Team BuildingRecommended100 mins€ 390.00€ 293.00
Clinical Events Committee (CEC) EstablishmentRecommended90 mins€ 360.00€ 270.00
Data Safety & Monitoring Board (DSMB) EstablishmentRecommended90 mins€ 360.00€ 270.00
Adverse Event ProcessesRecommended77 mins€ 198.00€ 148.00
European Safety Reporting Requirements during Pre-Market clinical InvestigationsRecommended50 mins€ 148.00€ 111.00
US Safety Reporting Requirements during Pre-Market Clinical TrialsRecommended20 mins€ 59.00€ 44.00