Clinical Study Manager, PainQx Company

Reports to VP, Research & Development

Key Tasks

• Oversee data acquisition and entry at multiple research sites following study protocols.
• Work with PainQx Database Manager and other PainQx development personnel as required to make sure that data is being efficiently transferred to PainQx and meets data integrity/quality expectations.
• Responsible for feedback to clinical sites on data quality and completion of electronic data capture forms (eCRFs).
• Assist in identifying qualified sites for study participation.
• Maintain strong working relationships and effective communication with collaborating institutional study teams.
• Track key study metrics using tracking tools. Provide timely updates to PainQx Management.
• Implement Data Verification Monitoring Plans as necessary (if not fully covered by Site personnel).
• Monitor compliance with SOPs and FDA regulations as necessary (if not fully covered by Site personnel).
• Other tasks and responsibilities as assigned.

Position Requirements

• BS/BA in Life Science or related discipline.
• 3+ year’s pharmaceutical or medical device clinical study experience.
• Experience in clinically applied multisite research studies.
• Previous EEG based clinical study experience a plus.
• Strong interpersonal skills with attention to detail a must.
• Demonstrated proficiency with word processing, spreadsheet, database, and presentation software (MS Office skills such as Outlook, Word, Excel, PowerPoint, SharePoint).
• Operate effectively in a multi-disciplinary, team-oriented culture.
• Willingness to continually embrace personal and professional development.
• Comfortable working in a fast-paced start up environment.
• Ability to periodically travel to clinical study sites.

Jobkey:
299
Program:
MassChallenge Boston 2017 Accelerator
Job Type:
A full-time permanent position
Application Email:
office@PainQx.com
Startup:
PainQx