Medical Information Specialist / Medical Writer. Job in Ridgefield LilyLifestyle

Ridgefield, CT

Contract Duration: 12 months

Rate: Negotiable

Salary: NA, $1.00

Responsibilities

Excellent employment opportunity for a Medical Information Specialist/Medical Writer in the Ridgefield, CT area.

Creating and updating scientific resources (e.g. FAQs and standard response documents) to ensure complete, accurate, balanced and referenced materials to respond to medical information inquiries from healthcare professionals and patients

Reviewing and updating existing medical information documents to ensure consistency across products and with the global medical information style guidance

Performing ad hoc literature searches

Contributing to the ad hoc development of customized responses to respond to specific HCP inquiries

Contributing to the development and maintenance of managed care formulary dossiers

Creating and updating slide decks while tailoring the content to the needs of diverse audiences (e.g. Call Center personnel, field-based representatives, etc.)

Performing peer review and fact check for Therapeutic ManagersSupport the completion of miscellaneous team tasks/deliverables which may include but is not limited to:

Developing new processes to support rollout of the new Global Medical Information system

Updating department Job Aids

Uploading content into the Medical Information database

Experience

PharmD ( preferred ) or other clinically oriented healthcare-related degree (e.g. BSPharm/RPh, NP, PA, PhD, or MD) from an accredited school or college earned prior to the start date at company.

1-2 year medical/drug information experience or medical writing (pharmaceutical industry experience is preferred but not required)

Experience in cardiology, metabolism, or respiratory is strongly preferred. Immunology and oncology experience is desired but not required.

Strong proficiency in providing accurate scientific/medical writing for a variety of scientific resources (e.g. FAQ, standard response documents, AMCP formulary dossier, slide decks) with a strong attention to detail

Ability to understand and summarize clinical data

Proficiency in navigating internal documents such as clinical trial protocols and clinical trial reports

Ability to perform MEDLINE and EMBASE literature searches

Excellent verbal and written communication skills

Strong computer skills, including Outlook, Word, PowerPoint, and Excel

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