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CVS Health Medical Writer in Boston, Massachusetts

Bring your heart to CVS Health. Every one of us at CVS Health shares a single, clear purpose: Bringing our heart to every moment of your health. This purpose guides our commitment to deliver enhanced human-centric health care for a rapidly changing world. Anchored in our brand — with heart at its center — our purpose sends a personal message that how we deliver our services is just as important as what we deliver. Our Heart At Work Behaviors™ support this purpose. We want everyone who works at CVS Health to feel empowered by the role they play in transforming our culture and accelerating our ability to innovate and deliver solutions to make health care more personal, convenient and affordable.

Position Summary

The Medical Affairs Clinical Evidence Medical Writer will play a pivotal role to support the execution of a strategic portfolio through the development of clinical evidence that demonstrates the effectiveness of our products, programs, and services. This position will work directly with the Executive Director of Clinical Evidence Development (CED) to design, develop, support, and manage cross-enterprise evidence generation from ideation through drafting and submission of clinical evidence deliverables (e.g., manuscripts, conference abstracts, and white papers).

This position will be a key member in research workstreams to prepare or assist in the preparation of study protocols from cross-functional teams, manage IRB submissions, critically analyze content for data validity and integrity, draft evidence deliverables (e.g., manuscripts, conference abstracts, white papers, decks, posters, podium presentations, visual abstracts), and support additional steps throughout the Medical Affairs governance process for clinical publications. Under the direction of Principal Investigators, the candidate will work with biostatisticians, clinicians, researchers, and other stakeholders to effectively and accurately communicate findings to a variety of audiences and be able to support its creative design. The candidate will ensure all evidence deliverables are generated in accordance with internal best practices, regulatory guidelines, and clinical research and medical writing standards. This position will also support the maintenance of a clinical evidence repository.

This position will work closely with CVS cross-enterprise partners from Analytics & Behavior Change, Product Teams (e.g., Digital, Virtual Care, etc), Health Equity Office, Medical Management, and other stakeholders to execute clinical evidence deliverables as part of an enterprise-wide evidence development strategy to impact clinical / scientific communications internally and externally.

Required Qualifications

  • 5+ years of experience as a Medical Writer.

  • Relevant work experience writing deliverables in healthcare and/or clinical research and supporting project management of cross-functional teams with large research portfolios with concurrent studies

  • Prepare, edit, and finalize protocols, synposes, regulatory documents and related clinical documents such as abstracts, posters, presentations, and manuscripts

  • Participate in scientific communication planning, including development of strategic medical communication plans and timeline development

  • Partner with colleagues to engage early with the study team including participation in the review of mock and/or blinded tables, figures, and listings, and narrative planning for relevant documents

  • Schedule and conduct document-related meetings including the preparation of pre-meeting agenda, key data points for discussion, and post-meeting minutes

  • Manage the document review process ensuring conflicting and/or ambiguous comments are clarified and appropriately addressed

  • Ensure appropriate documented quality control (QC) checks are performed on medical writing deliverables, responds to findings, and recommends quality process improvements

  • Demonstrated experience with research protocols and regulatory bodies, Institutional Review Board requirements, and Good Clinical Practices

  • Demonstrated experience in clinical research execution to interpret study results and collaborate with stakeholders in the development of clinical evidence development content

  • Demonstrated success publishing in scientific/clinical conference proceedings and major scientific journals

  • Bachelor’s degree in medical-related, life sciences, or relevant field

Preferred Qualifications

  • Master’s degree or higher in medical-related, life sciences, or relevant field

  • Experience with real-world data sources, study design, and evidence generation

  • Demonstrated ability to provide analytical review of clinical content management to ensure data integrity and validity

  • Relevant experience to support the development, maintenance, and querying of a clinical evidence repository

  • Excellent oral / written communication skills following the prioritization, identification, critical appraisal, and development of clinical evidence

  • Strict attention to detail

  • Oustanding time management skills; demonstrated ability to establish priorities, manage shifting priorities, and handle numerous time-sensitive projects with multiple deadlines

  • Demonstrated experience working independently and as part of a team

  • Excellent interpersonal relationship skills including negotiating and relationship management skills with the ability to drive achievement of objectives

  • Certified Society of Clinical Research Associate or Association of Clinical Research Professionals certification

  • Good Clinical Practice certification

  • Responsible Conduct of Research certification

  • Human Subjects Research certification

  • Research Study Design certification

  • Experience with Knowledge Management (e.g., EndNote, Electronic Databases) systems

Education

  • Bachelor’s degree in medical-related, life sciences, or relevant field (required)

  • Master’s degree or higher in medical-related, life sciences, or relevant field (preferred)

Pay Range

The typical pay range for this role is:

$60,300.00 - $132,600.00

This pay range represents the base hourly rate or base annual full-time salary for all positions in the job grade within which this position falls. The actual base salary offer will depend on a variety of factors including experience, education, geography and other relevant factors. This position is eligible for a CVS Health bonus, commission or short-term incentive program in addition to the base pay range listed above. In addition to your compensation, enjoy the rewards of an organization that puts our heart into caring for our colleagues and our communities. The Company offers a full range of medical, dental, and vision benefits. Eligible employees may enroll in the Company’s 401(k) retirement savings plan, and an Employee Stock Purchase Plan is also available for eligible employees. The Company provides a fully-paid term life insurance plan to eligible employees, and short-term and long term disability benefits. CVS Health also offers numerous well-being programs, education assistance, free development courses, a CVS store discount, and discount programs with participating partners. As for time off, Company employees enjoy Paid Time Off (“PTO”) or vacation pay, as well as paid holidays throughout the calendar year. Number of paid holidays, sick time and other time off are provided consistent with relevant state law and Company policies. For more detailed information on available benefits, please visit jobs.CVSHealth.com/benefits

We anticipate the application window for this opening will close on: 03/31/2024

CVS Health requires certain colleagues to be fully vaccinated against COVID-19 (including any booster shots if required), where allowable under the law, unless they are approved for a reasonable accommodation based on disability, medical condition, religious belief, or other legally recognized reasons that prevents them from being vaccinated.

You are required to have received at least one COVID-19 shot prior to your first day of employment and to provide proof of your vaccination status or apply for a reasonable accommodation within the first 10 days of your employment. Please note that in some states and roles, you may be required to provide proof of full vaccination or an approved reasonable accommodation before you can begin to actively work.

CVS Health is committed to recruiting, hiring, developing, advancing, and retaining individuals with disabilities. As such, we strive to provide equal access to the benefits and privileges of employment, including the provision of a reasonable accommodation to perform essential job functions. CVS Health can provide a request for a reasonable accommodation, including a qualified interpreter, written information in other formats, translation or other services through ColleagueRelations@CVSHealth.com If you have a speech or hearing disability, please call 7-1-1 to utilize Telecommunications Relay Services (TRS). We will make every effort to respond to your request within 48 business hours and do everything we can to work towards a solution.

We are an equal opportunity and affirmative action employer. We do not discriminate in recruiting, hiring, promotion, or any other personnel action based on race, ethnicity, color, national origin, sex/gender, sexual orientation, gender identity or expression, religion, age, disability, protected veteran status, or any other characteristic protected by applicable federal, state, or local law.

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