CRC (Clinical Research Coordinator) Manager
Background
Trialspark is a software and technology company based in NYC that helps accelerate the discovery of new drugs and medical treatments by reimagining the clinical trial process. We are building a network of our own clinical trial sites and are looking to hire a lead to oversee a team of Clinical Research Coordinators.
Job Description
As an early stage employee, you'll be working in partnership with our Director of Clinical Operations and other members of our leadership team to provide mentorship and oversight to a group of Clinical Research Coordinators. We are looking for people who are interested in contributing ideas about ways we can integrate services, practices, software, and technology to make clinical trials a better experience for patients, coordinators, CROs and sponsors.
Core Responsibilities:
- Mentor and manage a team of CRCs of varying experience levels for your assigned region
- Provide regional oversight of assigned staff to ensure proper adherence to Trialspark policies and procedures
- Contribute to the delivery of CRC training and development programs
- Contribute to the design and delivery of team capacity management system
- Perform regular performance evaluation and identify opportunities for staff advancement and development
- Develop and monitor individualized retraining plans or performance improvement plans
Relevant Experience
- ACRP or SOCRA-certified
- Ideal candidate has 1-3 years of experience supervising the activities of Clinical Research Coordinators or Clinical Research Associates
- Candidates with an equivalent combination of high-level, collaborative project work, peer mentorship and training experience may also be considered
- You have experience running or monitoring industry-sponsored trials at clinical trial sites and have a good sense of what can go wrong at sites
- You are organized and diligent
- You are a nice, practical and forward-thinking person with great communication skills
- You are comfortable with technology (have worked with the major IVRS, EDC platforms)
- You are interested in thinking about how clinical trial processes can be improved using new workflows, software, or technologies.
You will receive consideration for employment without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability, age, or veteran status.