Freelance Writing Jobs : Edmonton, Alberta

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14
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Cambridge, MA - Join bluebird bio’s enthusiastic and collaborative team by contributing to the overall success of our novel gene therapy approach. Reporting to our Vice President, Medical and Technical Writing, the primary deliverables for this role are clinical regulatory documents according to applicable regulations. It is envisioned that this person will play a leadership role in future key regulatory submissions to the FDA and EMA. About the role: Provide leadership in planning and completing key... to prepare protocols, clinical study reports, Investigator’s brochures, safety updates, and IND clinical sections in CTD format under strict timelines Participate in recruiting and mentoring of staff, and budget planning About you: PhD in a Life Science or equivalent At least 5 years in medical writing, including participating in submissions to the US FDA (NDA, BLA) and EMA (MAA), with supervisory experience Experienced in the preparation of protocols, study reports, investigator brochures...
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18
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CUNY Hunter College - New York City, NY - Writing Center Director (Provost Office) Job ID: 19897 Location: Hunter College Full/Part Time: Full-Time Regular/Temporary: Regular This position reports to the Assistant Vice President of Academic Initiatives. Responsibilities include, but are not limited to: Oversee the Writing Center staff, budget, physical space and technologies. Implement and oversee principled practice across various tutoring modalities. Design and implement assessment of service together with Center staff... and outside consultants. Interview, hire, on-board and develop tutoring staff in close collaboration with other members of the staff. Design and provide in-center, in-class and program specific workshops for courses across the curriculum. Coordinate Center funding sources and create/implement yearly budgets. Coordinate with various college offices to provide consultation and services. Co-coordinate (with a faculty member) the College’s Writing across the Curriculum (WAC) Program. As WAC Co-coordinator...
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16
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CURE International, Inc. - Michigan - opportunities within fixed guidelines, research country- and context-specific conditions and statistics, and assist in writing grant proposals. This internship is unpaid, and can be either part-time or full-time. The timeframe for the internship is Spring 2019 (approximately March 2019 - May 2019). CURE will support college credit, upon request. Responsibilities include: Complete prospect identification, research, proposal development and writing in conjunction with other CURE co-workers. Complete...CURE has an exceptional opportunity for a Grant Writing Intern (Spring 2019). This position represents a unique opportunity for students to gain practical work experience and increase their understanding of relevant issues related to their field of studies. The Grant Writing Intern will assist with the identification of appropriate grantors, and the execution and submission of grant requests. As part of a growing grants management office, the Grant Writing Intern will research funding...
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29
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Ardent Technologies, Inc. - Austin, TX - Role: Programmer with exp Writing complex programming code Location: Austin. TX Duration: 1+ years Client: Texas Office of the Attorney General (OAG 7 years Performs advanced systems analysis, development and design using technical knowledge of computer and information systems in web and mobile environments; design, develop, integrate, implement, and maintain multiple mobile/web application platforms, system modifications and backend application interfaces for data and services 7 years... and design 4 years Experience with the following: Responsive Web Design, Selenium WebDriver, Eclipse based IDEs, Rational ClearCase, Rational Software Architect or other Rational IDEs, WebSphere Portal, WebSphere Application Server, CSS, RESTful Web Services, Reactjs 1 year Texas Child Support Program 1 year Texas Child Support Enforcement System - provided by Dice Writing complex programming code, Performs unit testing, supports system testing...
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10
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San Francisco, CA - We are seeking an experienced Sr. Manager / Associate Director, Medical Writing to join Atara Bio. The successful candidate is responsible for clinical regulatory documents and other clinical content across the Atara Bio product pipeline. This position collaborates with a variety of functional areas to prepare and deliver documents and content in support of global regulatory filings and covering all phases of clinical development. Reports to Director, Medical Writing Remote location in... to other regulatory documents and publications. Drives the document development process from gathering materials and developing scientifically rigorous content to facilitating document review meetings and discussions and assuring adherence to electronic submission standards. Contributes to building the medical writing function through the development of internal processes, procedures, and templates. May prepare safety and scientific/technical documents and support clinical study transparency and disclosure...
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27
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Meet Recruitment - Boston, MA - Our client, a leading multinational Biopharmaceutical company, is currently seeking an Associate Director to head up their Medical Writing department. Headquartered in Boston, MA, this client provides a rewarding, hands on environment for their employees - even those at more senior management levels. This is the perfect opportunity to join a passionate, dedicated team whose mission is to change the lives of patients and families affected by rare diseases. Job Overview • Prepare, manage... documents or sections of documents written by internal and contract writers Skills Required • MS degree in life sciences; advanced degree in relevant clinical/regulatory field preferred 5+ yrs of medical writing experience combined with relevant pharmaceutical industry experience Regulatory knowledge and experience with regulatory submissions and global trials Experience developing, implementing, and measuring the impact of medical writing processes across multiple projects Proven excellence in...
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Boston, MA - Position Summary This position is accountable for the timely preparation of high quality, regulatory-compliant clinical document deliverables for Alexion. This position will support the medical writing (WM) activities for one or more clinical programs. This position will function with moderate supervision. The scope of this position includes the writing, document management, and development support for clinical study-related documentation including, but not limited to, clinical study..., styles, and processes. Clinical document types include clinical study protocols, clinical study reports, Investigator’s Brochures and updates, and other IND/CTA or global regulatory submission documents Supports development and implementation of strategy for writing and completion of high quality clinical documents Manages the writing and completion of documents and other assigned tasks within established timelines (editing and QC) and with highest quality in terms of scientific content...
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21
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Novartis - East Hanover, NJ - Head for Regulatory Writing in Innovative Medicines (Pharma and Oncology). 2. Manage quality, timeliness, efficiency and high scientific standards for written and electronically published regulatory documents produced by the group and for global teams, across geographical boundaries. 3. Oversight of all functional and operational activities for the development of documents for early and full development programs and commercial products within GDD. Ensure synergies between programs and divisions...
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25
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General Dynamics - Groton, CT - experience with submarine systems. Previous technical writing experience or technical work documents or formal work packages Skills Skills Candidates must have the ability to review and comprehend engineering drawings and technical data, as well as be familiar with shipbuilding specifications, technical manuals and other source documents related to test documentation. Familiarity with working with PC based systems and/or software required. Proficiency with Excel and Word is desired...
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25
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San Francisco, CA - This position will lead scientific, medical and regulatory writing activities for all development projects, ensuring full life-cycle support from clinical study protocols through regulatory submission and post-approval activities, and that documents are written in compliance with all regulations (ICH, GLPs, and GCPs). The professional will also perform the review, edit, and writing of documents and be responsible for the management, planning and direction of a team of medical writers. The... professional will provide mentoring and career development to the medical writing team; will ensure the timely presentation/dissemination of clinical data from investigational pipeline products according to budget, timelines, strategic publication plans, and tactical approaches; and ensures that strategically aligned scientific communication points are delivered and that statements and conclusions in publications (manuscripts, abstracts, posters, oral presentations, etc.) are accurate and supported...
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