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Senior Clinical Data Scientist- Emea Wide

hace 2 semanas

Barcelona, España Syneos Health Clinical A tiempo completo

**Description**

**Senior Clinical Data Scientist**

Come discover what our 25,000+ employees already know: work here matters everywhere. We’re a growing and evolving biopharmaceutical industry leader, which means you’ll have endless opportunities to work with experts around the world and build the career you’ve dreamed of.
As a part of the Syneos Health team, you’ll help us deliver results for a rewarding reason - we improve patients’ lives around the world. Because to us, a patient isn’t just a number, they’re our family, friends, and neighbors.

**Why Syneos Health**
- #SyneosHealthLife means we’re committed to our Total Self culture - where everyone can authentically be themselves. Our Total Self culture is what unites us globally, and we know every person’s unique contributions make a difference.
- We believe our success is a direct result of the people who are driving it - you We value your dedication to care for our customers and patients, so we want to focus on taking care of you. That’s why we offer a comprehensive benefits program encompassing your total health - physical, mental and financial.
- We are continuously building the company we all want to work for and our customers want to work with. Why? Because when we bring together diversity of thoughts, backgrounds, cultures, and perspectives - we’re able to create a place where everyone feels like they belong.

**Job responsibilities**
- Serves as Functional Lead for Clinical Data Science including primary contact for internal liaison between Clinical Data Science and Project Management, Clinical Monitoring, and other functional groups
- Acts as central steward of clinical data quality, monitors risks through the holistic review of clinical and operational data, using high level knowledge of the protocol, taking into account the specific therapeutic area aspects of the protocol related to the data collected and aligning with cross functional operational plans to drive comprehensive clinical data quality
- Ensures the required data elements and corresponding data quality oversight steps are identified to support the defined study analysis
- Works with assigned project teams to communicate, address, troubleshoot and resolve data related questions and recommends potential solutions; escalates issues which potentially impact patient safety and study analysis
- Coordinates cross functional data cleaning activities to ensure quality standards and timelines are met for clinical data deliverables Ensures the required data elements and corresponding data quality oversight steps are identified to support the defined project analysis
- Drives the development of the clinical data acquisition plan and corresponding data flow diagram with the study team, assess risks associated with protocol design, study set parameters that could impact the credibility and reliability of the trial results, aligns data flow with the study protocol to ensure data collected meets regulatory and study endpoint requirements.
- Drives the development of analytical tools, utilizes analytical platform/dashboard to detect potentially unreliable data that may impact the validity of the trial results Performs analytic reviews as defined in scope of work and data acquisition plan, identifies root cause to systematically resolve data issues
- Monitors and communicates project progress to the Sponsor and project team including use of project status reports and tracking tools/metrics
- according to contractual agreement and relevant Standard Operating Procedures (SOPs), guidelines, and regulations
- Review, maintain budget and identify out of scope for Clinical Sciences activities, raise to PM to be implemented in required change order
- Plans, manages, and requests Clinical Data Science resources for assigned projects
- Coordinates the work of the assigned Clinical Data Science team
- Develops and maintains project plans, specifications, and documentation in line with SOP requirements
- Maintains documentation on an ongoing basis and ensures that all TMF filing is up to date for necessary files
- Participates in, and presents at internal, Sponsor, third-party, and investigator meetings on behalf of clinical data science responsibilities
- Prepares input, and participates in proposal bid defense meetings and request for proposals on behalf of clinical data science responsibilities
- Plans for and creates necessary documentation to support internal and external audits; participates in such audits on behalf of clinical data sciences responsibilities
- Trains and mentors new or junior team members
- Maintains proficiency in Clinical Data Science systems and processes through regular training. May attend/represent the company at professional meetings/conferences
- Performs other work-related duties as assigned. Minimal travel may be required (up to 25%)

**Qualifications**

**What we’re looking for**
- BA/BS in the biological sciences, computer sciences, mathematics, o