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Worldwide Clinical Trials
Worldwide Clinical Trials
1 001 – 5 000 Darbuotojai
H1B vizos rėmėjasKonsultavimasLogistikaSveikatos priežiūra
Worldwide Clinical Trials yra pasaulinė sutartinių klinikinių tyrimų organizacija, padedanti farmacijos ir biotechnologijų įmonėms viso vaistų kūrimo ciklo metu. Daugiau nei 30 metų patirtį turinti įmonė teikia klinikinės stebėsenos, duomenų valdymo, pacientų įdarbinimo ir reguliavimo konsultavimo paslaugas tokiose terapinėse srityse kaip onkologija, kardiologija ir retosios ligos. Jos požiūris derina plačią klinikinių tyrimų kompetenciją su individualia pagalba ir sudėtingiems tyrimams pritaikytais sprendimais.
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Senior Clinical Database Programmer

Configure, test, and validate clinical databases while developing SAS programs for clinical data management. Support sponsors, study sites, and data management teams at Worldwide Clinical Trials.

INIndijaHibridinisVisas etatasVyresnysis specialistasPrivaloma Kalba: anglųPrograminės įrangos inžinierius

Aprašymas

  • Coordinate database configuration, maintenance, and validation across systems and applications.
  • Work with colleagues to assign tasks, set timelines, track progress, and flag open issues.
  • Train and mentor Clinical Database Programmers in database setup and SAS program development, testing, and execution.
  • Train and mentor Data Management staff in database and SAS program specifications.
  • Review project-specific data entry software specifications, including edit checks.
  • Review validation plans for edit checks and reconciliation checks.
  • Develop, test, and run SAS programs for data validation, reconciliation checks, listings, and transfers in clinical data management.
  • Configure internal and third-party database and eDC software for Data Management teams, sponsors, and sites.
  • Test databases and related applications against IT and Data Management standard operating procedures.
  • Run database upload programs and review error reports.
  • Work with third-party vendors to resolve software issues and implement changes.
  • Coordinate electronic data transfers with sponsors or their representatives.
  • Help Data Management create and maintain system procedures and documentation.
  • Support Quality Assurance activities and audit requirements.
  • Carry out other assigned duties.

Reikalavimai

  • Degree-level education or equivalent relevant experience.
  • At least five years of experience with data management systems and software.
  • Understanding of CDISC SDTM standards.
  • Experience programming in SAS.
  • Strong written and verbal communication skills.
  • A methodical, logical approach to solving problems.
  • Ability to learn new tasks quickly.
  • Careful attention to detail.
  • Ability to question the validity of data being entered or extracted.
  • A hardworking and efficient approach.
  • Strong teamwork skills.
  • Customer focus, dependable delivery, relationship building, communication and influencing skills, and openness to innovation and change.
  • Computer literacy and numeracy.
  • Willingness to adapt to different computer systems.

Privalumai

  • Equal employment opportunity.
  • A diverse and inclusive workplace.
  • Supportive, collaborative teams.
  • Training and mentoring opportunities.
  • Professional development through work on innovative clinical data management projects.

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