InterSources
***PLEASE HAVE CANDIDATES COMPLETE THE WRITING EXAM AND INCLUDE RESPONSES AT TOP OF RESUME: FULL DOCUMENT ATTACHED FOR DOWNLOAD***
Role is fully REMOTE and the candidates can reside anywhere in the US, but working in CST/EST time zones is preferred
Our team is guided by the company's mission to build a healthier place for us all to live and age in, and we are passionate about solving the hardest problems in the US healthcare system. If you're looking for a rewarding career with the opportunity to work with a highly motivated and experienced cross-functional team, this is the role for you.
You will be responsible for clinical workflows used by 10,000 clinicians nationwide, with a specific focus on clinician experience, clinical documentation integrity, and the resulting member experience of the clinical encounters.
We are looking for someone with: •Three to five years of experience as a technical writer; Medical writing, Clinical editing, or clinical data integrity experience a definite plus •Demonstrated ability to translate complex technology and clinical language in a simple and engaging manner •A strong foundation in the principles and best practices of technical writing and content design •Ability to blend traditional technical writing skills with technical knowledge and logic to recommend and implement clinical workflow changes for a more efficient and clinically accurate workflow. •Expert research and interviewing skills with the ability to communicate effectively with technical & clinical SMEs •Excellent writing, editing, and proofreading skills with a strong ability to tailor to varied audiences. •Bachelor's degree with a concentration in Technical Writing, English, Computer Science, or another related field; Masters degree is a plus •Relevant writing samples required
This role will report to our Sr. Director, Program Integrity and Optimization within the product organization.
What will you do? •Collaborate with developers, product managers, UX designers, and other SMEs to create thorough and accurate implementation requirements •Work closely with a small development team & emerging content management system to implement clinical content & logic in support of our clinical workflows •Attend daily standups and sprint planning for clinical workflow projects to track development progress •Regularly communicate progress and expectations with stakeholders •Diligently create and maintain all technical and release documentation related to the clinical workflow; including change logs, release notes, FAQs, and reference materials for several audiences (internal, external, technical, non-technical) Country Code US Experience Level Level II (3-5 Years) Is Hardware Required? Yes
Role is fully REMOTE and the candidates can reside anywhere in the US, but working in CST/EST time zones is preferred
Our team is guided by the company's mission to build a healthier place for us all to live and age in, and we are passionate about solving the hardest problems in the US healthcare system. If you're looking for a rewarding career with the opportunity to work with a highly motivated and experienced cross-functional team, this is the role for you.
You will be responsible for clinical workflows used by 10,000 clinicians nationwide, with a specific focus on clinician experience, clinical documentation integrity, and the resulting member experience of the clinical encounters.
We are looking for someone with: •Three to five years of experience as a technical writer; Medical writing, Clinical editing, or clinical data integrity experience a definite plus •Demonstrated ability to translate complex technology and clinical language in a simple and engaging manner •A strong foundation in the principles and best practices of technical writing and content design •Ability to blend traditional technical writing skills with technical knowledge and logic to recommend and implement clinical workflow changes for a more efficient and clinically accurate workflow. •Expert research and interviewing skills with the ability to communicate effectively with technical & clinical SMEs •Excellent writing, editing, and proofreading skills with a strong ability to tailor to varied audiences. •Bachelor's degree with a concentration in Technical Writing, English, Computer Science, or another related field; Masters degree is a plus •Relevant writing samples required
This role will report to our Sr. Director, Program Integrity and Optimization within the product organization.
What will you do? •Collaborate with developers, product managers, UX designers, and other SMEs to create thorough and accurate implementation requirements •Work closely with a small development team & emerging content management system to implement clinical content & logic in support of our clinical workflows •Attend daily standups and sprint planning for clinical workflow projects to track development progress •Regularly communicate progress and expectations with stakeholders •Diligently create and maintain all technical and release documentation related to the clinical workflow; including change logs, release notes, FAQs, and reference materials for several audiences (internal, external, technical, non-technical) Country Code US Experience Level Level II (3-5 Years) Is Hardware Required? Yes