REMOTE ROLE: Clinical Information Specialist - III (Senior) Job at The Fountain Group, Jersey City, NJ

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  • The Fountain Group
  • Jersey City, NJ

Job Description

PAY $66-75/hour W2. W2 Candidates only, C2C not possible with this client.
This is a remote role, no expectation of onsite work.
Part time role 10-15 hours per week.

Manager Notes
  • The external meetings this individual would need to attend are usually 7 or 8 EST in addition to meetings with Organon team in the mornings US time.
  • So ideally would like someone in EST Zone.
  • At least 5 years experience leading the design, strategy, and implementation of eCOA platforms in support of study endpoint data.
  • No specific eCOA platform is required.
  • Participate in study team meetings, provide expert input on eCOA/ePRO design, strategy, reporting, user testing, etc.
Original Job description:
  • Responsible for collaborating with internal and external stakeholders to ensure that the software solution captures the necessary data points for data extraction, visualization, and real-time integration, implementing optimal eCOA processes, and building and improving relationships with eCOA/ePRO providers.
  • Regularly meets with internal and external teams to discuss open and emerging business issues related to eCOA/ePRO projects and systems, makes recommendations for improvements, and leads on their implementation.
  • Provide expert input, ensuring that clinical protocols are appropriately mapped to solutions efficiently, accurately and within project scope.
  • Identifies, develops, implements, and reviews effectiveness of current and new eCOA processes, including for new services, in collaboration with others.
  • Perform and support the UAT of the eCOA/ePRO configurations with necessary documentation.
  • Collaborates in the investigation of study issues found beyond the start-up phase of the study, especially the CAPA process with cross-functional teams.
  • Reviews and analyzes current metrics to identify trends and suggest process improvements.
Qualifications:
  • Four-year college/university degree in computer science, engineering, life science, or healthcare related field with at least 5 years of experience working with clinical trials or in pharmaceutical industry.
  • Ability to understand and interpret clinical trial documentation such as protocols, questionnaires and other data collection instruments, and clinical data models.
  • Five or more years demonstrated experience leading and implementing eCOA projects across multiple platforms. (Experience in women health is a plus)
  • Advanced computing skills, including experience with TRADOS or other translation management tools (CAT, or Computer Aided Translation tools) and eCOA vendor working files (e.g., JSON, XML,)
  • Knowledge of regulatory standards/guidance for eCOA/ePRO
  • Demonstrated experience leading teams in a matrix working environment across projects.

Job Tags

Remote job, Part time, Day shift,

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