We are currently seeking to expand our network of team members to lead and support client projects in a consulting capacity. Our projects are well suited for candidates who have pharmaceutical industry experience with a deep understanding of GCP. Candidates must have thorough knowledge of new regulatory requirements for proactive risk management, including sponsor obligations for oversight of service providers.
Candidates need a deep understanding of:
Our team members who fulfill consulting activities are experienced industry professionals who are able to perform gap analyses and design and implement solutions in an effective and fit-for-purpose way. Our team members utilize Avoca’s library of tools to propose solutions for clients to fill gaps. They are adept in managing internal teams to meet client needs. An ideal candidate will have substantial knowledge of clinical research, with expertise in relevant specialty areas such as quality systems, risk management, outsourcing models, effective oversight, clinical operations, and change management. They will have the ability to review and edit leading practices and documents to match ICH E6 (R2) and other regulatory requirements.
The ideal candidate must be self-driven with a sense of urgency and the ability to work effectively and independently in a virtual company environment. We find that successful team members are passionate about bringing solutions to the industry and have a desire to make a tangible difference for our clients. The ability to manage client expectations and look at issues through a business development lens is preferred.
Clinical Operations professionals work virtually; however, travel to client locations is required on an as-needed basis.
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