Senior Medical information Writer (Director level)

Employvision Inc.; United States; Remote; USD 56,000 - 105,000; Full time

Job summary

A leading pharmaceutical company seeks a Senior Medical Information Writer to develop high-quality medical content. Responsibilities include creating FAQs, managing content development, and collaborating with clients to ensure compliance. Candidates must hold a relevant degree and have substantial experience in medical writing within the pharmaceutical industry. The role requires excellent communication skills and the ability to work under tight deadlines.

Qualifications

• Minimum 2 years experience in pharmaceutical industry or Medical Information.
• Proficient editing skills along with experience in technical writing.
• Strong understanding of regulatory requirements.

Responsibilities

• Develop medical content including FAQs, Scientific Response Documents, and educational materials.
• Drive the document development process and collaborate with clients.
• Manage quality issues and ensure compliance with industry standards.

Skills

Excellent communication skills

Scientific writing

Project management

Interpersonal skills

Analytical thinking

Education

Doctorate or Master of Science (MSc) in Life Sciences or healthcare

Tools

Microsoft Office

Adobe Acrobat

PubMed

EndNote

Job description

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Title: Medical Information Writer -Senior

Location: Remote in USA

Duration: 3 -6+ months

We are looking for medical writing help. Especially someone who has experience in medical information deliverables such as FAQs and standard response documents.

• Hours per week: 20 to 30 hours, with flexibility to work up to 40 hours if needed
• An important aspect of medical information is developing, managing, and providing impactful medical response documents. This position is responsible for medical content development-related client engagements.

This role requires medical information and medical content experience and knowledge, including excellent communication skills (both verbal and written),

Medical information and Content Development experience

ESSENTIAL DUTIES AND RESPONSIBILITIES:

Our employees are tasked with delivering excellent business results through the efforts of their teams. These results are achieved by:

• Plays an essential role supporting Global Medical Information / Medical Content
• Development Team on content development-related engagements for clients who require medical content development and management services.
• Writes and creates medical and scientific content related to Medical Affairs, Medical Information and Medical Communications including, but not limited to, Scientific Response Documents (SRD), Frequently Asked Question (FAQ) documents, Slide Sets, Abstracts, Posters, Education and Training materials, and others for potential clients.
• Drives the client document development process from gathering materials and developing scientifically rigorous content to facilitating document review and discussions at medical, legal, regulatory (MLR) review meetings.
• Works with company and/or client-provided document management technology platforms (i.e., Veeva PromoMats / MedComms, etc.) as content owner when appropriate, uploading documents, providing reference anchoring and annotations as required.
• May be called up to perform scientific data fact checking for documents in support of medical reviewers participating in MLR teams.
• Collaborates with Global Medical Information / Medical Content Development Team and contributes to discussions on strategy, tactical execution and communication approaches for assigned projects.
• Provides direction and works closely with other medical writers and medical content development team to deliver on client projects efficiently and effectively.
• Participates in key client meetings as assigned.
• Supports creating/updating the SOPs, checklists, templates, style guides, and guidance documents as necessary.
• Stays knowledgeable of industry best practices and supports leadership team in evaluating and implementing new technologies and procedures to improve operational efficiency and quality of materials developed.
• Works collaboratively with other medical writers and creative teams across.
• All other duties as assigned
• Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions of this position.

EXPECTATIONS OF THE JOB:

• Responsible to work collaboratively with company's medical information and medical affairs team and take direction and feedback from management and clients
• Responsible to ensure management and compliance with industry standards and codes of practice
• Able to work independently to develop high-quality, scientifically accurate, strategically aligned, ethical, and compliant medical content
• Responsible to proactively flag and manage any quality issues, and ensure timely corrective and preventive actions
• Travel This position may require business travel and will need to be able to travel up to approximately 10-15%.
• Hours: Able to work full time and be flexible with work scheduling as required by clients and management.
• The above list reflects the general details necessary to describe the expectations of the position and shall not be construed as the only expectations that may be assigned for the position.

An individual in this position must be able to successfully perform the expectations listed above.

MINIMUM KNOWLEDGE, SKILLS AND ABILITIES:

The requirements listed below are representative of the experience, education, knowledge, skill and/or abilities required.

Education:

Doctorate or Master of Science (MSc) degree in Life Sciences or healthcare or equivalent.

Experience and/or Training:

• A minimum of 2-year(s) experience in pharmaceutical industry or Medical Information / Medical
• Communications service provider. Experience developing global medical information materials, e.g., scientific response documents (SRDs), frequently asked questions (FAQs), custom response documents (CRDs), etc.
• Exceptional written, oral, interpersonal, and presentation skills including the ability to independently interpret and summarize complex results. Ability to establish credibility with a variety of audiences; especially with clients
• Ability to effectively interface with all levels of management and staff and to succeed in a matrix team setting while meeting or exceeding timelines.
• Proficient editing skills along with expertise in Microsoft Office, Acrobat and other applications.
• Experience conducting literature searches and working with tools such as PubMed, Ovid, Embase, etc.
• Experience working with reference management and citation software (e.g., EndNote, Mendeley, Citavi, etc.)
• Strong understanding of regulatory requirements and best practices in relationship to Medical Information, Medical Affairs and promotional and non-promotional materials review
• Excellent project management skills and proven track record of being results driven
• Ability to conceptualize, design and deliver best in class solutions.

PREFERRED QUALIFICATIONS:

Education: A Pharm.D. or Pharm.M or a Degree in Medicine or PhD is preferred. Relevant Bachelor’s Degree in a Life Science also considered.

Experience: Medical Information, Medical Communications, Medical Writing, Medical Affairs; experience developing medical content, especially Medical Information materials, for both new product launches and for updating and managing current materials; experience working across multiple therapeutic areas.

Communication Skills: Possesses the ability to develop and articulate ideas and information that generate understanding and creates a climate that motivates and encourages others to participate.

Analytical Thinking / Critical Thinking: Ability to analyze, digest, and interpret complex scientific information and data

Project Management:Ability to develop project plans and execute on the project plan, both works individually and working with client(s), other medical content development team members, and medical information contact center team and leadership team.

Results Driven:Proven track record of executing and delivering results.

Innovator: Transforms creative ideas into original solutions that positively impact client delight and company’s performance.

Highly Principled: Proves to be a professional of unquestionable integrity, credibility and character who demonstrates high moral and ethical behavior.

Client Management:Ability to manage, coordinate, and oversee relationship and projects with assigned client(s).

Seniority level

• Seniority level

  Mid-Senior level

Employment type

• Employment type

  Contract

Job function

• Job function

  Writing/Editing, Art/Creative, and Science

• Industries

  Pharmaceutical Manufacturing

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