Bioequivalence Data Management Specialist

🏢 MARC
📍 6th of October City, EgyptFull-timeOn-site
📅 Posted: 3w ago🔄 Updated: 3w ago
CV%
✨ AI Summary
MARC for Medical Services and Scientific Research is seeking an experienced Bioequivalence Data Management Specialist to join their team. This role involves preparing Clinical Study Reports (CSRs), designing and generating Electronic Case Report Forms (eCRFs), and performing data reconciliation. The specialist will also be responsible for preparing study protocols, maintaining study documentation, and ensuring compliance with study protocols, SOPs, and GCP guidelines. A Bachelor's degree in pharmacy and at least 1 year of bioequivalence experience are required, along with strong organizational, teamwork, and communication skills.
Required Skills
Information Technology
Data Management
Other
clinical study reportselectronic case report formsstudy protocolsgood clinical practice (gcp)
Finance, Legal & Governance
Bank Reconciliation
Soft Skills & Professional Competencies
Attention to DetailCollaborationCommunication
Requirements
Bachelor’s degree in pharmacy.Minimum of 1 year of experience in the bioequivalence field.Good organizational skills with strong attention to detail.Ability to work effectively within a team environment and meet study timelines.Good written and verbal communication skills.
Description
MARC for Medical Services and Scientific Research is an integrative research center that aims to advance science by conducting research in interdisciplinary disease areas. Our goal is to conduct high-priority and ethical basic, preclinical and clinical research, bridging the gap between science and community to improve health and quality of life.MARC is looking to have an experienced candidate for Bioequivalence Data Management SpecialistKey responsibilities:Prepare Clinical Study Reports (CSRs) and related study documents.Design and generate Electronic Case Report Forms (eCRFs).Perform data reconciliation activities in accordance with study-specific procedures.Prepare study protocols and associated documentation.Maintain study documentation, data tracking logs, and study records.Ensure compliance with study protocols, company Standard Operating Procedures (SOPs), and Good Clinical Practice (GCP) guidelines.
✨ Premium Match Details
Deep-dive CV analysis, customized Cover Letters, and Interview prep!
📊 Match Analysis
Insights against your active CV
📊
Personalized Match Analysis
Upload your CV to see exact matching percentages, detailed skills mapping, and gap analysis for this role.
🎯 Overalli74%
⚡ Skillsi85%
View Breakdown
Ontology Match: 85.0
Matched:✓ Requirements Matching✓ Ontology Skills Mapping
📜 Eligibilityi49%
View Breakdown
Local: 19600%
🏗️ Career Fiti91%
View Breakdown
Seniority: 91.0
📋 Requirementsi67%
View Breakdown
Domain: 67.0
🔥 Motivationi78%
View Breakdown
Title Fit: 78.00