Clinical Data Specialist I

Job Title: Clinical Data Specialist I
Location: This position is based in our Campbell, California offices. This position is hybrid and full time.

Why Imperative Care?
Do you want to make a real impact on patients? Imperative Care is changing the way stroke is treated. As part of our team, you’d be developing breakthroughs that will revolutionize the future of stroke care. Every day, the technologies that we develop at Imperative Care directly impact human lives. Our focus is on the needs of the patient, and they come first in everything we do.

What You’ll Do
This entry level professional is responsible for supporting activities associated with the data management process throughout a clinical trial. This includes participation in the development and building of electronic Case Report Forms (eCRFs), eCRF Completion Guidelines (CCGs) and Data Management Plans (DMPs) that reflect the requirements of study protocols in partnership with Clinical. The role will assist with additional data management activities (e.g., User Acceptance Testing (UAT), data review and external vendor reconciliation).

• Assist in set-up, build, and test of electronic data capture system and clinical trial management system
• Assist in determining database specifications per study requirements and support in implementation
• Take part in development of clinical data management plans and other related documents
• Understand study protocol, review related study documents, data collection forms and SOPs
• Generate data extracts for data review and reporting
• Participate in other data management activities, such as query management, user access management
• Performs database User Acceptance Testing, including scripting writing and execution
• Verifies site compliance with electronic data capture requirements and with oversight verifies required clinical data entered in the case report form (CRF) is accurate and complete.
• Support senior team members with tasks of routine difficulty, where close guidance or supervision is received Actively promote and support the Quality Management System, Quality Objectives, and Quality Policy.

What You’ll Bring

• Bachelor’s degree in a science related discipline and less than 2 years of professional experience; or equivalent combination of education and work experience in the medical device or related regulated industry

• Some working knowledge in EDC, CTMS and eTMF systems
• Understanding of GCP, GCDMP, CFR regulations in an IDE setting preferred
• Demonstrate good time management skills
• Attention to detail
• Excellent communications skills (both written and verbal) required
• Ability to work independently or in team setting required
• Ability to travel 10-30% for the role

Employee Benefits include a stake in our collective success with stock options, competitive salaries, a 401k plan, health benefits, generous PTO, and a parental leave program.

Join Us! Apply Today.

Salary Range: $73,000 - 77,000 annually 
Please note that the salary information is a general guideline only. Imperative Care considers factors such as scope and responsibilities of the position, candidate's work experience, education/training, key skills, and internal equity, as well as location, market and business considerations when extending an offer.