Sr. Data Scientist (Clinical Data Management) - Remote
Premier Research helps highly innovative biotech and specialty pharma companies transform life-changing ideas into reality, targeting unmet needs in analgesia, neuroscience, oncology, pediatrics, and rare diseases.
We’re looking for an exceptional Senior Data Scientist to bring your passion to our team. You will be encouraged to grow professionally and personally while enjoying cross-functional partnerships with genuinely supportive colleagues, regardless of location or seniority. Most importantly, you will be using your skills to bring tangible hope to critically ill patients around the world.
At Premier Research, we are science-minded and heart-centered. Join us.
As a Lead Data Scientist with Premier Research, you’ll have the opportunity to work closely with the Project Manager as the point of contact for all data management responsibilities on multiple studies, including serving as the program or portfolio manager for a key client.
What you’ll be doing:
- Oversee the preparation of data management plans, data entry guidelines, data management reports and other documents required for preparing and completing databases
- Review draft protocols and CRFs for potential data collection and representation, database structure or data entry problems, and provides feedback to the project team; review CRFs, data listings, and database to ensure all captured data follow the rules outlined by the protocol and data management plan; track data as they are processed through the study lifecycle
- Generate queries to appropriate internal or external personnel (investigational sites, vendors, Clinical Research Associates, client representatives) to resolve problematic data identified during every aspect of the data management process
- Review responses to queries for appropriateness, resolves any discrepancies and modifies the database accordingly
- Mentor Data Coordinators and junior Leads
- Support new business opportunities, including contribution to study budgets, proposals, and bid defense meetings
You’ll need this to be considered:
- Minimum of a Bachelor's Degree, preferably in Science, Engineering, or Math, or RN, RPh, or LPN certification preferred along with a minimum of 5 years of mastery in data management/science/analytics/informatics and at least 2 years leading studies
- Proven expertise in ICH/GCP and/or ISO14155 requirements; knowledge of site and institution specific contract requirements; clinical trials support or pharmaceutical industry experience; working knowledge of medical terminology and experience with clinical research; working knowledge of FDA Guidance Documents and clinical monitoring procedures; proficient in the development and review of Informed Consent Form templates
- Understanding and experience at least one Database Management System (e.g., Medidata Rave, DataLabs EDC, Oracle RDC or Inform, etc.); knowledge of web-based communication tools for conferences
- Known for being customer-focused in approach to work and communications with the ability to professionally Interact with site, clients, vendors and other functional areas; strong verbal and written communication and negotiation skills
- Maintains a positive, results-oriented work environment; excellent team player, collaborative and able to build an effective team.
- Excellent organizational and time-management skills, able to prioritize work to meet deadlines; ability to multitask and work effectively in a fast-paced environment with changing priorities; accountable, dependable and strongly committed.