Senior Science/Medical Writer

2 weeks ago

United Kingdom Parexel Full time

Parexel is in the business of improving the world’s health. We do this by providing a suite of biopharmaceutical services that help clients across the globe transform scientific discoveries into new treatments. From clinical trials to regulatory, consulting, and market access, our therapeutic, technical, and functional ability is underpinned by a deep conviction in what we do.Patients First, Quality, Respect, Empowerment & Accountability.
We looking for a Senior Medical Writer's due to an ever expanding team. These roles can be fully home based in various European countries.
As the Principal Medical Writer you will research, create, and edit all documents associated withclinical research. You will operate as the project lead writer/submission coordinatorand primary client contact to manage contributions of multiple writers working on related documents. You will alsofacilitate process improvement and technical mentoring/training and supportMedical Writing Services management during the sales process by providing client liaison and proposalsinput.
Gather, review, analyze, and evaluate pertinent resources to prepare, develop, and finalize clinical documents for submission to regulatory authorities, including but not limited to: briefing documents, investigator brochures, study protocols, model informed consents, interim and final clinical study reports, common technical document (CTD) clinical overviews and summaries, safetyupdate/aggregate reports, and integrated summaries of safety and efficacy.
-Revise document drafts based on the review comments from team members to ensure inclusion of all relevant input.
Quality Control
- Ensure that all work is complete and of high quality prior to team distribution or shipment to client.
- Provide medical editing review of draft and final documents prepared by other writers before internal or external distribution. This includes both copyediting and content review.
Project Management
- Operate as the project lead writer/submission coordinator and primary client Management contact to manage contributions of multiple writers working on related documents. Manage scope of work, timeline and project goals, technical information, and input from clients throughout the project.
- Provide leadership and strategic planning/adjustments, delegation of responsibilities, and tasks to team members.
Respond appropriately to incidents of dissatisfaction, and feed back to Medical Writing Services management.
- Provide support as appropriate to Business Development/Client Solutions and Medical Writing Services management in their efforts to win new business. Identify and solicit new business leads for Medical Writing Services, attend business development meetings, and prepare and make sales presentations to clients, if called upon.
Training/Compliance
-Keep abreast of new advances in medical writing and regulatory issues.
- Develop and train Medical Writing Services staff to enhance writingquality, efficiency, and project management.
- Comply with departmental procedures and requirements, such ascompletion of project assignment and workload trackers on the applicablesoftware platform
- Analyze efficiency of work and discuss improvement ideas with Medical WritingServices management and colleagues.
Bachelor's degree in Life Sciences/Health Related Sciences or equivalent
A flexible attitude with respect to work assignments and new learning.
-Exhibits sound judgement: escalates issues to project teams or departmental management as appropriate. Ability to negotiate on behalf of medical writing to ensure resources, timelines and expectations are aligned.
-Establishes a connection with the client beyond one's project, to gain repeat business and/or to widen existing scope and services. Demonstrated understanding of clinical research, the drug development process, and industry guidelines and regulations, e.g., Extensive clinical/scientific writing skills acting as either a Senior Medical Writer or PrincipalMedical Writer
-Scientific background essential; writing experience includes multiple clinical documents: study reports, study protocols, or CTD documents or similar.
-Advanced word processing skills, including MS Office (expertise in Word); software and systems knowledge or ability to learn and adapt to various IT systems: document management systems, collaborative authoring (e.g., SharePoint), and file conversion and databases (Excel).
-Fluent in written and spoken English with appropriate attention to phraseology, grammar, and punctuation.
In return we will be able to offer you a structured career pathway and development within the role including awareness and understanding of the industry. Your hard work will be rewarded with a competitive salary, bonus and a benefits package including holiday, pension, bonus and other leading edge benefits that you would expect with a company of this type.
LI-REMOTE #J-18808-Ljbffr

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