Medical Writer

ApotheCom

About The Position

ApotheCom, an Inizio Medical company, is a medical communications leader drawing on experience across pharmaceutical research, marketing, medical and regulatory writing, sales, publishing, digital media, and design. The Medical Writer uses scientific expertise to develop and deliver medical communications projects. The work includes reviewing and interpreting preclinical and clinical research, creating scientific materials according to project briefs, synthesizing clinical trial data for physician and consumer audiences, and keeping medical information accurate and current. The role works with international pharmaceutical clients and may involve interaction with scientists and physicians, client meetings, teleconferences, and scientific meetings. Travel is required as needed, including weekends. The position is open to candidates seeking a fully remote or hybrid opportunity based in the United States. ApotheCom describes its working environment as friendly and informal and offers career and personal development opportunities, flexible benefits, personal support, and learning and development opportunities. The company states that it is committed to equal opportunity, diversity, inclusion, and belonging.

Requirements

Advanced degree in life sciences, pharmacology, or medicine.
Previous medical writing experience within a medical communications agency or pharmaceutical environment.
Excellent written, verbal communication, and interpersonal skills.
Ability to thrive in a fast-paced environment, meet deadlines, and manage multiple projects.
Strong financial, administrative, and organizational skills, including the ability to multitask.
Keen attention to detail and ability to prioritize responsibilities and work both in a team-oriented environment and independently.
Advanced computer skills, knowledge of Internet searches, and proficiency with Microsoft Windows software, including Word, Excel (including maintaining complex spreadsheets), and PowerPoint.

Responsibilities

Review and interpret data from preclinical and clinical research articles to create scientific written materials in line with project briefs.
Work with international pharmaceutical clients and interact with scientists and physicians on therapeutic and scientific issues.
Remain current with medical developments and conduct literature searches to ensure accurate medical information for assigned projects.
Participate in client meetings and teleconferences and attend scientific meetings as required.
Synthesize clinical trial data and translate its relevance for physician and consumer audiences according to client requirements.
Travel as needed, including weekends.