Senior Clinical Content Developer

Full-time
North Miami, Virtual
Posted 2 months ago

The Senior Clinical Content Developer supports the development and maintenance of the clinical content of Carevive’s Products. Using medical literature review and in collaboration with the Carevive Clinical Strategic Solutions experts, this role’s primary responsibility is to produce clinical content that represents best practice standards and will meet requirements for different users, applications and contexts.  The Senior Clinical Content Developer is also responsible for quality assurance (QA) of the content.

Reports To: VP, Clinical & Research Operations

Essential Responsibilities/Duties/Functions/Tasks:

  • Utilizing the principles of evidenced-based medicine (EBM), develop, and update clinical content through the appraisal and synthesis of information gathered from the medical literature, clinical experts and professional sources of practice guidelines (e. NCCN, AJCC, etc…)
  • Perform Quality Assurance review and testing of clinical content
  • Partner closely with the product team to determine clinical prioritization of projects and content development in collaboration with members of the content development team
  • Provide content review and appraisal of data integration processes in collaboration with configuration and integration team
  • Participate in content development meetings and weekly meetings of clinical and product development teams
  • Manage internally and externally written content to ensure that it meets Carevive’s quality standards and is in alignment with client expectations and medical/legal/regulatory requirements/processes
  • Ensure appropriate syntax, style, and content flow for different product types and target audiences (including various clinical providers, patients and caregivers) amend or rewrite content as needed
  • Provide timely, consistent and constructive feedback to writers and other contributors
  • Direct content through appropriate review, configuration and quality review/testing processes, to ensure on-time delivery of accurate content quality; ongoing collaboration with the configuration team to translate content to the platform.

Qualifications (Education & Experience):

  • Licensed Healthcare professional (e.g., RN, NP, PA, PT, OT, SLP, Psychologist, LICSW) with license in good standing required
  • Clinical oncology certification required
  • 7+ years clinical oncology experience required
  • Healthcare technology experience in a start-up environment preferred
  • Experience and understanding with agile product management is a plus
  • Research and Evidence Based Medicine (EBM) knowledge or experience highly desirable
  • Writing experience highly desirable
  • Experience with AMA style referencing, ability to adapt to house style/format
  • Ability to learn new technologies and concepts quickly
  • Ability to multi‐task and work on simultaneous projects
  • Proficiency in Microsoft Office Professional products, including but not limited to MS Word, Excel, Visio
  • Excellent verbal/written communication, interpersonal, and customer service skills
  • Ability to set and manage priorities judiciously
  • Excellent written and oral communication skills
  • Ability to articulate ideas to both technical and non-technical audiences
  • Superior analytical, evaluative, and problem-solving abilities
  • Must be results oriented; effective as both a team member and independent worker with attention to detail and ability to multi-task

Job Features

Job CategoryClinical, Research
Job Id425

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