An internet marketing company is in need of a Telecommute Legal Marketing Content Writer. Core Responsibilities of this position include: Developing informative, engaging, well-researched content for the clients’ websites.
Exceptional writing skills. Solid critical thinking and problem solving abilities. Entrepreneurial spirit and a passion for supporting and promoting partner relationships. Superior communication skills. Strong knowledge of Payment Processing industry.
Core Responsibilities Include: Lead and grow a team of writers and development editors serving the Higher Education market. Supervise/manage overall projects. Work closely with publishers to develop and create educational products. Qualifications Include:
Expertise in liaising with the EEOC, writing position statements, conducting internal investigations, and providing positive resolutions regarding claims, inquiries or complaints. High level of technical experience, working on multiple computer systems and platforms daily.
Managing a team of contributors in order to inspire greatness. Position Requirements Include: Knows his or her SEO inside and out. Deeply analytical to make data-driven decisions at all times. Understands how to write for a real human, and that quality content is king.
Thorough knowledge of ICH and local regulatory authority regulations regarding drug research and development. Read, write, and speak fluent English. Undergraduate degree or its international equivalent in clinical, science, or health-related field from an accredited institution.
Writing and developing ad concepts for online fundraising campaigns, Launching and monitoring campaigns across self-served media partners. Qualifications Include: 3 or more years of marketing, advertising, fundraising, or digital organizing/political experience.
Travel a minimum of 4 times per year, within the US, to medical/nursing society meetings. 5 years experience in health/non-profit sector. Proficient in Microsoft Office (Word, PowerPoint, Excel) Experience in developing, writing successful proposals – foundation and federal.
Demonstrable experience in writing or editing protocols, study reports and/or abstracts. Excellent knowledge of ICH/GCP/FDA/MHRA and other region and/or country specific regulations and guidelines.
Must be a licensed health care professional (i. e. registered nurse) or equivalent work experience required. Must read, write and speak fluent English and be fluent in host country language. Strong experience in clinical trial management as a CM. Experience in managing complex or global trials.