Study Activation Coordinator
Passionate about precision medicine and advancing the healthcare industry?
Recent advancements in underlying technology have finally made it possible for AI to impact clinical care in a meaningful way. Tempus' proprietary platform connects an entire ecosystem of real-world evidence to deliver real-time, actionable insights to physicians, providing critical information about the right treatments for the right patients, at the right time.
Do you find the slow pace of drug development unacceptable? Are you ready to use cutting-edge technology to accelerate the completion of cancer clinical trials? Do you want to be a change agent for cancer patients? We are performing just-in-time (JIT) study activation much better and faster than ever before. We are looking for experienced clinical trials professionals who have innovative ideas and want to put them into action.
What You’ll Do
- Execute aggressive JIT study activation deadlines for pharma-sponsored oncology trials in the TIME Trial national network of cancer research sites.
- Employ your industry expertise, and emotional intelligence to integrate seamlessly with study activation teams with sponsors, CROs, vendors and sites.
- Work closely with internal teams to design and track documents and processes required for planning and execution of rapid activation.
- Demonstrate your foresight and critical thinking skills to identify critical pathways, proactively mitigate risk, troubleshoot problems and escalate to decision-makers when needed.
- Utilize your attention to detail to track and report key metrics
- Collaborate with bioinformatics, product development, data analytics, sales and business development to provide superior customer service for sites and sponsors
- Actively contribute to continual quality improvement by helping to develop development of innovative tactics, processes, tools, systems, and strategies to continually accelerate the completion of cancer clinical trials
- Wear multiple hats and support new roles, teams, projects and products as business needs evolve.
Qualifications:
- Bachelor's Degree
- Exceptional customer service skills and strong interpersonal and problem-solving skills
- Proven track record of setting and achieving high personal standards of performance
- Highly organized and systematic, superb attention to detail, and ability to complete tasks with a high degree of accuracy and an eye towards process improvement
- Flexible and adaptable; ability to work independently in a fast-paced environment
Preferred Qualifications
- Previous experience working with study activation from a site, sponsor or CRO perspective
- Familiarity with FDA regulations, GCP, drug development processes, clinical site, and trial operations.