Who we are:
Bevov is building a platform to connect BioPharma professionals with interesting opportunities within the BioPharma industry without having to search for them. We have the largest network of BioPharma companies who are looking to connect with the right candidate without having to go through the hurdles of multiple job applications and not getting to hear back from them. Our platform’s goal is to provide a positive candidate experience by companies showing interest in you instead of you applying to them, matching you with the right job with competitive and flexible compensation, and helping you through the interview process via our platform and SuperRecruiters.
Responsibilities
• Collaborating with VP, Clinical Operations to set targets for selected CROs, and ensuring the planning and execution of trial(s) in compliance with SOPs, CFR, ICH, and GCP guidelines as well as applicable local regulations and project goals.
• Reviewing and approving study-specific clinical plans, tools, and documents.
• In conjunction with VP, Clinical Operations, building the trial budget and overseeing the trial budget through forecasting and actuals.
• Reviewing and approving site selection in conjunction with relevant internal team members.
Oversight of study start-up, ongoing management, and close-out of all CROs and vendors. May act as main contact or support for assigned studies.
• Project Management of assigned vendors to ensure adherence to schedule management, communication management, and quality management.
• Providing Clinical Research Associates/Assistants with project-specific training.
• Ensuring proper tracking, management, and reporting of clinical trial progress, risks, and data cleaning activities.
• Arranging and overseeing site visits, as needed.
• Direct line management responsibilities for Clinical Research Associates/Assistants may be responsible for more senior employees as part of their career development.
Qualifications
• Bachelor’s degree in nursing or life sciences and 5+ years of work experience for pharmaceutical, biotech or CRO, or a similar company. In the absence of a bachelor’s degree, sufficient work experience in the relevant field to compensate will be considered.
• Willingness to learn – more interested in ‘getting it right than in ‘being right.
• Ability to flex and work in a dynamic environment
• Solid understanding of clinical trial activities
• Outstanding communication skills, both verbal and written.
• Proficient with Microsoft Office Word and Excel.
• Ability to work independently and prioritize duties.
• Understanding of Electronic Data Capture (EDC).
• Available to travel (expected travel % no more than 20%
