A Black Diamond Networks client is looking for a senior-level project manager with at least 10 years of experience managing clinical & regulatory projects/programs. This client is not looking for a clinical trial manager, instead the consultant will be working on managing timelines and providing high-level oversight as to what needs to be done next to drive the projects forward. The consultant's primary responsibility will be overseeing the writing of clinical documentation, as the client is still in the early stages in the clinical trials process. This will not be a hands on position, but one that's more concerned with overall strategy and driving the project through to completion. Candidates for this position must have a background in clinical and/or regulatory affairs, as the consultant will be helping out both sides. Regulatory filing/strategy experience is preferred. PMP or oncology experience is a huge plus. Bachelors Degree required.
Project and or program management experience.
Experience working within a clinical & regulatory setting.
At least 10+ years of relevant work experience.
Experience managing tight deadlines, while driving projects forward to completion.