Senior Data Scientist - Literature

Senior Data Scientist - Literature (m / f / d)-Information Science / Pharmaceutical / research / development / Pharmacovigilance / Medical / Drug / Biomedical / synthesize scientific data / Competitor Information Access Platform / DIALOG / English

Project :

For our pharmaceutical customer based in Basel, we are looking for a Senior Data Scientist - Literature (m / f / d)

Background :

The Senior Data Scientist - Literature in the Safety Analytics and Reporting (SAR) group of the Safety Risk Management function (PDS) supports Roche products and is responsible to provide literature searches for global literature monitoring purposes and retrieval of information from biomedical databases to answer medical inquiries on the safety of our medicinal products and devices. The group also provides other biomedical literature searches in Pharma Development (PD) (eg : for PD Medical Affairs to identify the efficacy of company's medicinal products for the following purposes : Periodic Safety Update Reports (PBRER)). The criticality of these deliverables (eg mandated from regulators) requires that standards, timelines, quality and needs from customers in Clinical Science, Safety Operations, Medical Affairs (PDMA), Regulatory and other functions are achieved. Results of the analyzes form a key component for a patient focused risk management. She / he supports projects and contributes to the Safety strategy through projects, services and involvement in strategic initiatives.

The perfect candidate

The ideal candidate possesses an MS or University degree in medicine, pharmacy, or natural sciences, paired with a minimum of two years of Information Science experience specifically within Pharmacovigilance and drug development. They must be a self-motivated team player with excellent analytical thinking, communication, and training skills, ensuring timely and compliant delivery of search results while proactively improving processes and fostering strong cross-functional relationships.

Tasks & Responsibilities :

• Performs ad-hoc literature searches in biomedical databases to identify adverse drug reactions and risks in association with company's medicinal products and devices.
• Develops, tests, documents and maintains literature search profiles to identify published case reports of adverse drug reactions in association with company's medicinal products.
• Develops, tests, documents and maintains search profiles to identify adverse drug reactions and risks in association with company's medicinal products for the following purposes : Development Safety Update Reports (DSURs), Periodic Benefit-Risk Evaluation Reports (PBRERs) and signal detection.
• Develops, tests, documents and maintains search profiles to identify incidents and risks in association with company's medical devices for the following purposes : Medical Device Incident Reports (MDIR) and signal detection.
• Performs efficacy searches in biomedical databases for PDMA to identify the efficacy of company's medicinal products for the following purposes : Periodic Safety Update Reports (PBRER).
• Maintains effective relationship with customers in PDS and beyond Interacts with customers to define the search criteria for literature searches.
• Checking the results of literature searches for plausibility.
• Ensure timely and correct delivery of search results.
• Performs literature searches in compliance with Standard Operating Procedures.
• Acts as core member in Safety Literature Group, active contribution to knowledge sharing.
• Creates training material for team members and stakeholders on retrieval and reporting related topics and delivers the training
• Proactively raise ideas and identify opportunities to enhance ways of working (including processes, methods, technologies etc.). and share best practices and lessons learned with peers.
• Establish, promote and maintain effective working relationships with other Roche stakeholders, departments and functions as required.
• Ensures any issues relating to literature searches are adequately addressed at the lowest level and escalated appropriately.

Must Haves :

Reference No . :

Role : Senior Data Scientist - Literature (m / f / d)

Industry : Pharma

Location : Basel

Workload : 100%

Start : ASAP(Latest start date : )

Duration : 9Months

Deadline :

If this position has sparked your interest, please send us your complete application via the link in this advertisement. If this position is not a good fit for your profile and you would like to receive information about other positions directly, you can also send us your application via this advertisement or to jobs[at]itcag[dot]com.

Contact us for more information about our company, our positions or our attractive payroll-only program :

About Us :

ITech Consult is an ISO 9001 : 2015 certified Swiss company with offices in Germany and Ireland. ITech Consult specializes in placing IT candidates for contract work. Founded inby IT professionals, we understand the importance of professional support in project searches and work.

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