Mga Trabaho sa ClinChoice sa Pilipinas

Safety officer responsible for performing regulatory monitoring and reporting safety issues to local health authorities. · ...

Safety officer responsible for performing regulatory monitoring and reporting. · ...

ClinChoice is a partner to the largest pharmaceutical innovators in the world. We provide expertise in clinical operations to help our partners advance healthcare. · ...

ClinChoice is a partner to the largest pharmaceutical innovators in the world. We provide expertise in clinical operations and help our partners advance healthcare by accelerating clinical trials with data-driven insights. · ...

Annotate Case Report Form following FDA/CDISC or sponsor guidelines. · Develop SDTM specifications and generate SDTM datasets using SAS; · Develop ADaM specifications and generate ADaM datasets using SAS based on Statistical Analysis Plan; ...

ClinChoice provides expertise in clinical operations to help partners advance healthcare by accelerating clinical trials with data-driven insights. · ...

This role involves performing intake/triage, data entry, and quality review for individual case safety reports from various sources. · ...

Annotate Case Report Form following FDA/CDISC or sponsor guidelines and develop SDTM specifications and generate SDTM datasets using SAS. · ...

We have forged future-defining partnerships with industry bodies and technology companies to develop cutting-edge solutions that deliver our expertise with quality and precision.ClinChoice is a partner to the largest pharmaceutical medical device and consumer care innovators in t ...

Job summary · Responsibilities include annotating Case Report Form following FDA/CDISC or sponsor guidelines and developing SDTM specifications. · QualificationsBachelor's/Master's degree in Statistics or related scientific disciplines with at least 4+ years of clinical programmi ...

As Senior Statistical Programmer develop SDTM specifications generate ADaM datasets using SAS create electronic submission packages to FDA. · Annotate Case Report Form following FDA/CDISC guidelines. · Develop SDTM specifications generate ADaM datasets using SAS. · Develop Tables ...

+Job summary · A senior statistical programmer will annotate case report forms following FDA/CDISC guidelines. · +Responsibilities:Annotate Case Report Form ) following FDA/CDISC or sponsor guidelines. · Develop SDTM specifications and generate SDTM datasets using SAS. · ...

We are seeking a skilled Senior Statistical Programmer to join our team! · Annotate Case Report Form following FDA/CDISC or sponsor guidelines. · Develop SDTM specifications and generate SDTM datasets using SAS. · Create electronic submission package to FDA, · e.g., , following F ...

ClinChoice is seeking a Medical Writer Associate to coordinate and compile data for PSUR reports while maintaining open communication with stakeholders. · Coordinate and compile relevant data to complete PSUR reports. · E nsure open communication with stakeholders throughout the ...

The role involves annotating case report forms following FDA/CDISC guidelines developing SDTM specifications generating ADaM datasets using SAS creating electronic submission packages following FDA guidelines with minimum supervision. · ...

ClinChoice is a partner to the largest pharmaceutical medical device and consumer care innovators in the world. · Provides medical expertise support and clarification of science as needed. · ...

We are seeking a Scientist Physician to provide medical expertise and support to our team. · ...

We are looking for a Medical Review Physician to perform medical review of non-serious & serious ICSRs with emphasis on seriousness, expectedness, causality & narrative etc. without missing on quality & compliance. · ...

Annotate Case Report Form following FDA/CDISC or sponsor guidelines.Develop SDTM specifications and generate SDTM datasets using SAS;Develop ADaM specifications and generate ADaM datasets using SAS based on Statistical Analysis Plan. · ...

Perform Intake/Triage, Data Entry, and Quality Review for individual case safety reports from a variety of sources including spontaneous literature regulatory and clinical trial cases. · ...