
Feasibility Site Specialist
We’re looking for an experienced Feasibility Site Specialist to join our team at PPD-Pharmaceutical Product Development. In this role, you’ll be responsible for evaluating potential sites for clinical studies and providing guidance to our clients on the selection of the most suitable sites for their clinical studies. We’re looking for someone with strong attention to detail and excellent problem-solving skills who is comfortable working independently and with teams in a fast-paced environment.To be successful in this role, you’ll need at least 5 years of experience in clinical research and/or site feasibility, as well as excellent communication and organizational skills. It’s also important that you have a strong understanding of the regulatory requirements for clinical research and experience working with electronic data capture systems. If you’re up for the challenge and meet these qualifications, we’d love to hear from you!
Responsibilities:
• Evaluate potential sites for clinical studies and provide guidance to clients on the selection of the most suitable sites for their clinical studies
• Conduct research and data analysis to identify potential sites that meet the client’s criteria and objectives
• Maintain accurate records of site evaluations and make recommendations to clients on the selection of sites
• Liaise with the clinical team to ensure that all regulatory requirements are met
• Monitor and assess the performance of sites throughout the clinical trial process
• Utilize electronic data capture systems to track data and ensure accuracy
• Maintain a high level of attention to detail and ensure accuracy of data
• Communicate effectively and collaborate with internal and external stakeholders
• Troubleshoot any issues or discrepancies that arise in the selection process
• Stay up-to-date with current regulations and industry trends related to site feasibility
Excellent Communication And Interpersonal Skills
Bachelor's Degree In Business Or Related Field
Experience In Clinical Trial Management
Knowledge Of Gcp/Ich Guidelines
Proven Ability To Assess Feasibility Of Clinical Sites To Support A Clinical Study
Ability To Prioritize And Manage Multiple Projects
Experience In Project And Budget Management
Ability To Work Independently And As Part Of A
Budgeting
Documentation
Research
Networking
Communication
Writing
Multitasking
Negotiation
Compliance
Technical
Collaboration
Analytical
Problem-Solving
Project-management
Report-Writing
Communication
Leadership
Problem Solving
Time management
Work ethic
Interpersonal Skills
creativity
Teamwork
Adaptability
organisation
According to JobzMall, the average salary range for a Feasibility Site Specialist is $50,000 - $95,000 per year. This salary range is highly dependent on factors such as the individual's experience, the size of the company, the location of the job, and the industry.
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PPD, Inc. is a global contract research organization providing comprehensive, integrated drug development, laboratory and lifecycle management services.

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