Clinical Data Manager F/M

Since 2002, Median Technologies has been expanding the boundaries of the identification, interpretation, analysis and reporting of imaging data in the medical world. Our core activity is to develop advanced imaging software solutions and platforms for clinical drug development in oncology, diagnostic support, and cancer patient care. Our software solutions improve the management of cancer patients by helping to better identify pathologies, develop and select patient-specific therapies (precision medicine).

The company employs a highly-qualified team and leverages its scientific, technical, medical, and regulatory expertise to develop innovative medical imaging analysis software based on Artificial Intelligence, cloud computing and big data. We are driven by our core values that are essential to us. These values define who we are, what we do, the way we do it, and what we, as Median, aspire to:
• Leading innovation with purpose
• Committing to quality in all we do
• Supporting our customers in achieving their goals
• Always remembering to put the patient first

Today, we are a team of more than 220 people spread worldwide in the US, Europe and China. Our company is growing in a fulfilling international and multicultural environment.

In the context of our development, we are looking for a: Clinical Data Manager M/F

The Clinical Data Manager contributes to MEDIAN drug development clinical trials for which The Clinical Data Manager handles Data Management tasks to insure a high level of quality and accuracy of the data.

o   Responsible of the quality of the data that is transferred all along the study: control the integrity and

the accuracy of the data

o   Responsible of the applications of the data management standards and regulations

o   Implements & applies the defined Clinical Data management processes: define, implement and

perform the verifications and reconciliations on the collected images and clinical data

o   Responsible for the computation and verification of the statistical data files in the context of the clinical

trials’ readers monitoring and data reconciliation

o   Bachelor's degree in clinical data management, bioinformatics or biomedical engineer.

o   Previous experience in clinical trial activities or pharma data handling (minimum 1 years)

o   Knowledge & Skills: Biology, clinical trials, GCP

o   Fluent in English: English communication skills (oral / written) are mandatory.

o   Qualities : Professionalism, open-mindedness, adaptability, good communications skills

Legal

o   Job location: China (home based or shanghai office)

o   Contract: 3-years’ short term contract

o   Start: ASAP

o   Offered salary: will depend on candidate’s skills and experience.