Planet Pharma
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https://www.propharmagroup.com
https://www.propharmagroup.com
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eCOA Technical Specialist
Posted: 02/06/2025
2025-02-06
2025-03-12
Employment Type:
Contract
Job Category: Project Management
Job Number: 617612
Is job remote?: Yes
Country: United States
Job Description
Target PR Range: 67-77/hr
*Depending on experience
Key Responsibilities include:
• Accountable for quality delivery and competencies within the eCOA service area
• Oversee study level system requirements meetings with eCOA vendors and internal stakeholders
• Assist in the design and development of study specific technical documents
• Support the internal team in managing project related timelines and associated activities
• Partner with data management (DM) to define the requirements for data transfers
• Work with external resources to manage the creation and execution of user acceptance tests
• Identify and track study-related technical issues to resolution
• Provide a supportive framework for continuous process and quality improvements
Basic Qualifications:
• Doctorate Degree OR
• Master's Degree and 3 years of Clinical experience OR
• Bachelor's Degree and 5 years of Clinical experience OR
• Associate degree and 10 years of Clinical experience OR
• High school diploma/GED and 12 years of Clinical experience
Preferred Qualifications:
• Bachelor’s Degree in life science, computer science, engineering, business or related discipline
• 4+ years of experience in clinical development
• Experience implementing clinical systems, such as CTMS, EDC, IVRS, ePRO or other related technology in the pharmaceutical/biotechnology industry
• Knowledgeable in Good Clinical Practices, and FDA regulations necessary
• Project management and technical expertise, attention to detail, and excellent documentation and communication skills
• PMP
• Previous vendor management experience
• Excellent time management and organization skills
• Have sound problem resolution, judgment, and decision-making abilities
• Be able to work well in a team-based environment with minimal supervision
*CO/NYC candidates might not be considered
*Depending on experience
Key Responsibilities include:
• Accountable for quality delivery and competencies within the eCOA service area
• Oversee study level system requirements meetings with eCOA vendors and internal stakeholders
• Assist in the design and development of study specific technical documents
• Support the internal team in managing project related timelines and associated activities
• Partner with data management (DM) to define the requirements for data transfers
• Work with external resources to manage the creation and execution of user acceptance tests
• Identify and track study-related technical issues to resolution
• Provide a supportive framework for continuous process and quality improvements
Basic Qualifications:
• Doctorate Degree OR
• Master's Degree and 3 years of Clinical experience OR
• Bachelor's Degree and 5 years of Clinical experience OR
• Associate degree and 10 years of Clinical experience OR
• High school diploma/GED and 12 years of Clinical experience
Preferred Qualifications:
• Bachelor’s Degree in life science, computer science, engineering, business or related discipline
• 4+ years of experience in clinical development
• Experience implementing clinical systems, such as CTMS, EDC, IVRS, ePRO or other related technology in the pharmaceutical/biotechnology industry
• Knowledgeable in Good Clinical Practices, and FDA regulations necessary
• Project management and technical expertise, attention to detail, and excellent documentation and communication skills
• PMP
• Previous vendor management experience
• Excellent time management and organization skills
• Have sound problem resolution, judgment, and decision-making abilities
• Be able to work well in a team-based environment with minimal supervision
*CO/NYC candidates might not be considered
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