Freelance Writing Jobs : Alpharetta, Georgia

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18
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Cambridge, MA - Summary: Residing in either our Boulder, CO or Cambridge, MA office, the Senior Medical Writer/Medical Writing Manager will work with internal cross-functional teams and contract research organizations (CROs) to draft and revise clinical study reports, NDA/MAA clinical summary documents, clinical protocols and investigator’s brochures to support regulatory filings in oncology indications. The Medical Writer will demonstrate flexibility and operate with a high degree of autonomy, working...
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Engility - China Lake, CA - of experience writing technical documents Secret Security Clearance or ability to obtain one The selected applicant will be subject to a government security investigation and must meet eligibility requirements for access to classified information. US Citizenship is required to meet this obligation PREFERRED QUALIFICATIONS: BA in related field 5 years of experience writing technical documents. Not ready to apply? for general consideration....
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MSD - Rahway, NJ - functional business plans of the clinical regulatory writing portfolio and contribute to the development of the group and the department’s objectives. - Manage priorities and assign internal and external medical writing resources, in alignment with business needs and staff developmental opportunities. - Provide scientific and operational guidance to medical writers, ensuring consistent application of standards and adherence to regulatory requirements and the timely completion of high quality... to department management through strategic input, continual process improvement, innovation, collaboration with internal and external stakeholders, and leadership for medical writing processes, standards, and initiatives. - Participate in budgeting, administration, and business objectives for their group. Qualifications Education: - Required: - Bachelor’s degree in life sciences or pharmacy with a minimum of 12 years of regulatory medical writing experience OR - Master’s degree...
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22
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Boston, MA - BRA/EDIC TITLE: WRITING AND INSTRUCTIONAL COACH STATUS: EXEMPT DEPARTMENT/DIVISION: WRITEBOSTON/ OFFICE OF WORKFORCE DEVELOPMENT SUMMARY OF RESPONSIBILITIES: Under the supervision and direction of the WriteBoston Director of Programming, carry out the mission and vision of WriteBoston through serving as a Writing/instructional coach at Madison Park High School and other WriteBoston middle/high schools and leading and developing professional development modules in collaboration... with the Director of Programming. WriteBoston offers training and coaching for teachers, coaches, and districts, along with writing opportunities for students, built on the premise that powerful writing and thinking are inseparable. WriteBoston provides high-quality professional development in writing instruction to middle and high school educators and administrators from district, charter, independent and technical-vocational schools in Massachusetts. GENERAL DUTIES AND RESPONSIBILITIES: The...
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27
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Mankato, MN - Responsibilities This position manages the writing, speech & language tutoring center at the Center for Academic Success (CAS), the primary source of academic support for students at Minnesota State University, Mankato. The Assistant Director assesses and develops writing, speech & language support for all students seeking academic support assistance. This position recruits, trains and evaluates peer tutors, maintains a high quality on-site and online tutoring program and provides direct... tutoring. The software to track, schedule & conduct both on-site and online tutoring is developed and maintained in conjunction with the Director and CAS staff. The Assistant Director collaborates with faculty, staff, administration and students to provide the delivery of writing support services, and helps to keep the CAS on the cutting edge of best practices and technology. This position provides academic advising to a select cohort of first year students. Required Qualifications Master's Degree...
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Collegeville, PA - --.and.gt;.and.nbsp; Title:.and.nbsp; Associate Director Clinical Writing.and.nbsp; Job ID:.and.nbsp; 1029810.and.nbsp; Location:.and.nbsp; United States-California-La Jolla; United States-Massachusetts-Cambridge; United States-New Jersey-Peapack; United States-Pennsylvania-Collegeville.and.nbsp; Full-Time.and.nbsp; Regular.and.nbsp; About Pfizer.and.nbsp; A career at Pfizer offers opportunity, ownership and impact.All over the world, Pfizer colleagues work together to positively impact health...
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10
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PRAHS - USA - : Overview: The Associate Director of Medical Writing oversees deliverables, supervises employees, and provides expertise in the area of regulatory writing, publications writing, and regulatory publishing. Responsibilities: Primary Responsibilities ? Ensures quality and timely production of departmental deliverables. ? Reviews project tasks and timelines and assigns team members. ? Leads project teams in the delivery of services to clients. ? Liaises with other functional managers... to ensure consistency of departmental approach within the company. Other Responsibilities: Interviews and selects team members according to sponsor needs. Takes a lead role in the development of department procedures and initiatives. Collaborates with other departments to identify, investigate, and implement new business opportunities. Coordinates writing activities with the project teams for document development. Provides strategic direction for regulatory writing, publication writing...
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Arlington, VA - . Position Description Seeking a Defense Contract Writing System subject matter expert who will assist in providing functional architecture input to Company Defense contract writing solution offering. Specific activities could include but are not limited to requirements analysis, functional specification creation, demonstration script writing and execution, test script and execution, training material development and delivery, and functional user support. Required Skills - Bachelor’s degree... -Minimum of 10 years’ experience with legacy Defense contract writing solutions (Standard Procurement System, CONWrite, PAADS, etc.) to include Federal Acquisition Regulation/Defense Federal Acquisition Regulation Supplement (FAR/DFARS) awareness. - Active Secret Security Clearance - Must be willing to travel 25% to Dayton, OH Desired Skills - Contract Writing System configuration....
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USA - A private nonprofit educational testing and assessment organization is searching for a person to fill their position for a Online Speaking and Writing Test Rater. Core Responsibilities of this position include: Evaluating essays Scoring responses holistically, evaluating the overall quality of thinking and writing against the Independent and Integrated Scoring Guides for Speaking and Writing Applicants must meet the following qualifications: B.A. or higher degree from an accredited...
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Lexington, MA - Position Summary This position is accountable for the timely delivery of high quality, regulatory-compliant clinical document deliverables for company. This position will lead the medical writing activities across a disease area or set of clinical programs. This position will also manage the medical writers at the Cheshire site. The scope of this position includes the management and oversight of clinical study protocols, Investigator’s Brochures, clinical study reports, and collaborate..., clinical contributions to briefing documents, health authority response documentation, pediatric investigational plans, and other IND/CTA or global regulatory submission documents, working cross-functionally and with minimal supervision Produces high-quality documents to meet aggressive timelines Ensures consistent messaging across all submission documents (nonclinical, clinical, and product labeling) Participates with Sr Dir Medical Writing to formulate writing strategies and standards...
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