Company Description
Medable's mission is to get effective therapies to patients faster. We provide an end-to-end, cloud-based platform with a flexible suite of tools that allows patients, healthcare providers, clinical research organizations and pharmaceutical sponsors to work together as a team in clinical trials. Our solutions enable more efficient clinical research, more effective healthcare delivery, and more accurate precision and predictive medicine. Our target audiences are patients, providers, principal investigators, and innovators who work in healthcare and life sciences.
Our vision is to accelerate the path to human discovery and medical cures. We are passionate about driving innovation and empowering consumers. We are proactive, collaborative, self-motivated learners, committed, bold and tenacious. We are dedicated to making this world a healthier place.
Job Description
Coordinate the overall Solutions Design process ensuring that the clinical protocols are appropriately mapped to software solutions efficiently, accurately and within project scope
In-depth knowledge of Medable's software, technology, and processes to be able to guide a client to the best use of Medable's platform to meet their needs
Develop and communicate design best practices for specific therapeutic areas
Participate in providing input related to Sales to Service, Kick-Off, Solutions Overview, Specification Review, and Software Review meetings
Explain complex technical topics in an easy to understand way to non-technical audience
Establish project timelines
Effectively work on teams and collaborate across multiple divisions within the company
Collaborate with product team to scope additional product features and product roadmap
Develop supporting documentation to streamline software design and configuration
Become an expert on technical concepts and software programs
Gather and document sponsor requirements and specify design components to support those requirements
Qualifications
Bachelor's degree in Computer Science or a related field
Minimum of 3 years of experience in the execution of clinical trials or a combination of education and experience
Microsoft Word, PowerPoint, Excel
Additional Information
Ability to understand and interpret clinical trial documentation such as protocols, clinical data models and other eClinical data collection instruments
Demonstrated experience in interpretation of client requirements to prepare and document design specifications
Detail-oriented and results-driven
Adept at solving complicated technical problems and conversing with clients
Excellent troubleshooting and creative problem solving skills
Ability to clearly document and track progress across many competing priorities
Ability to effectively organize and manage multiple assignments with challenging timelines
Ability to adapt and adjust to changing priorities
Positive attitude and the ability to work well with others
Demonstrated initiative and motivation
Ability to multitask and prioritize tasks
Effective at working with teams
Software experience (EDC or clinical trial software preferred)
Proven experience in client relations and interactions with clients at all levels
Excellent presentation, communication (written and oral) and negotiation skills
