Clinical Content Developer Lead

Full-time
North Miami, Philadelphia, Virtual
Posted 6 months ago

The Clinical Content Lead has a strong understanding of organization’s clinical content including patient care planning and patient and clinician facing products.  Works with clinical subject matter experts to develop product content and maintain accuracy of existing content.  Works with clinical expert consultants and content development team members to manage changes in clinical content.   Supports client services regarding content development and upgrades to effectively train users. Completes the content configuration documentation and oversees the product development process including configuration, quality assurance, testing and release.   Engages with staff from the research team regarding research project content development process.

Location:  Work from home office; Travel to onsite meetings, professional meetings and client sites (avg 1-2 trip monthly)

Reports To: Director, Clinical Product Development

Essential Responsibilities/Duties/Functions/Tasks:

  • Review editorial, scientific and clinical content of oncology literature for accuracy and relevance (including but not limited to: eLearning programs, scientific reviews, clinical journals, oncology practice guidelines, apps, digital journals)
  • Develop content needs assessments and develop clinical content based on principles of adult learning
  • Manage internally and externally written content to ensure that it meets Carevive System’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 and content quality
  • Assist in commissioning and contracting thought leader authors and editors, as needed
  • Participate in training and ongoing mentoring of junior team members
  • Participate in client clinical meetings, clinical team onboarding and adoption of content across specialty areas.

Qualifications (Education & Experience):

  • Masters-prepared nurse or higher clinical degree
  • Two or more years of clinical oncology experience required
  • Experience with AMA style referencing, ability to adapt to house style/format
  • Experience conducting/analyzing sources of clinical evidence to compile practice recommendations supported in high level evidence;  excellent analytic skills
  • Organized with the ability to prioritize and organize work, meet tight deadlines, adapt to shifting deadlines, and successfully function within a team environment
  • Strong communicator with superior writing and developmental editing skills
  • Proficiency with MS Word, PowerPoint, and Adobe Acrobat Pro required; knowledge of Adobe
  • Ability to successfully and efficiently interact with colleagues and external stakeholders at all levels: writers, editorial and support staff, clients/sponsors, and key members of the scientific/medical community

Job Features

Job CategoryProduct Management
Job Id369

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