Clinical Research Site Access Specialist
21 hours ago
**About Us**
At Emmes, we are transforming the future of clinical research by bringing the promise of new medical discovery closer within reach for patients. With over 47 years of experience, we have built industry-leading capabilities in cell and gene therapy, vaccines, infectious diseases, ophthalmology, rare diseases, and neuroscience.
We believe that the work we do will have a direct impact on public health initiatives, both globally and in our local communities. Our collaborative culture is at the intersection of being a performance-driven and people-focused company. We strive to build a team of talented professionals who share our motivations and passion for research.
**Job Summary**
The Clinical Research Site Access Specialist plays a key role in supporting the pre-award proposal and bid defense process. The specialist interrogates all relevant data sources and leverages analytics tools to define the optimal country/site/patient strategy for a clinical trial, including identification of key challenges and areas of opportunity.
**Responsibilities**
- In pre-award, develops and presents country/site/patient solutions by researching and analyzing data, writing proposal text, and participating in bid defenses.
- Works on realistic protocol prediction by analyzing patient profile, Standard of care, etc.
- Leads awarded feasibility offerings by confirming or revising the site and patient strategy and scope of work through discussions with the client and cross-functional team members, overseeing creation of the optimal site profile, creating site assessment surveys, reviewing data from sites, determining parameters for tiering sites, and providing PSV recommendations.
- Translates feasibility assessment data/results into visual presentations and/or written reports, as required, and delivers to internal/external stakeholders in the determined forum (e.g., client or team meeting).
- Performs other duties as assigned.
**Requirements**
- Bachelor's or Associate degree or local equivalent, in a life science, communication, and/or scientific discipline required.
- Master's degree in a life science, communication, and/or scientific discipline is strongly preferred.
- Must have 3 years' relevant experience in drug development with 1 year's experience in conducting at least one of the following: pre-award feasibility, post-award site identification/site selection/recruitment planning for global studies or have exceeded performance in the role of Global Feasibility Associate (minimum of 1 year) with strong experience in the functional role of feasibility (pre-award).
**What We Offer**
- A competitive salary range of $80,000 - $110,000 per annum.
- Flexible Approved Time Off.
- Tuition Reimbursement.
- 401k Retirement Plan.
- Work From Home Anywhere in the US.
- Maternal/Paternal Leave.
- Casual Dress Code & Work Environment.
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