Medical Writer 2

Medical Writer 2


Medical Writer 2

Details of the offer

IQVIA™ is the leading human data science company focused on helping healthcare clients find unparalleled insights and better solutions for patients. Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness the power of healthcare data, domain expertise, transformative technology, and advanced analytics to drive healthcare forward.

Minimum 5-7yrs of experience in medical writing with hands on investigator brochure, protocols, clinical study protocol.

Acts as Lead Medical Writer on more advanced writing projects and performs competently, with guidance from senior staff as required. Takes responsibility for preparation of assigned documents to a high standard, working in accordance with Quintiles SOPs and the customer's requirements. Identifies project needs, tracks project timelines and implements client requests with senior review.
Participates in both internal and external project team meetings and liaises directly with the customer on medical/technical writing issues, including setting of project timelines, as appropriate and with senior support as needed.
Facilitates appropriate internal review of assigned documents and takes responsibility for on-time delivery.
May perform QC review of documents or parts of documents prepared by more senior staff.
May deliver basic level training to small groups or individuals within Quintiles on the role of the medical/technical writing processes and specific client report templates, processes, and requests.
Takes responsibility for managing workload for assigned projects and tasks, in collaboration with senior staff.
Keeps abreast of current data, trends, medical and/or technical writing/regulatory knowledge, developments and advances in area of drug development/medical and/or technical writing.
Complies with Company SOPs and participates in the implementation of new SOPs.

Excellent standard of written English, and ability to communicate fluently and effectively in English, both in writing and verbally.
Familiarity with the structural and content requirements of clinical or method validation and study reports, protocols, and similar documents for internal and external clients.
Ability to integrate, interpret, and summarize data from a variety of sources in a clear and concise manner.
Competence in completing good first draft technical reports or clinical reports within a standard timeframe with limited guidance.
Good understanding of common statistical methods used in clinical trials or pharmaceutical work and/or interpretation of their results.
Ability to give a presentation to a project team and/or customer on project-specific topics, e.g. on lessons learned.
Ability to identify deficiencies, errors, and inconsistencies in a protocol or report.
Ability to effectively review a statistical analysis plan and to identify deficiencies, errors, and inconsistencies in statistical output as related to acceptance criteria according to SOPs.
Confidence in building relationship with customer and discussing medical/technical report writing issues with customers in person, via e-mail or on the telephone.
Can provide thorough, appropriate and sensitive feedback to peers upon request to review a document.
Ability to work on several projects at once while balancing multiple and overlapping timelines.


Ability to assess workload and suggest prioritization to senior staff.
Demonstrated abilities in collaboration with others and independent thought.
Knowledge of regulations relevant to medical writing/technical writing, such as Good Laboratory Practices (GLP) and

other relevant regulatory agencies (e.g., OECD, MHLW).
Careful attention to detail and accuracy.
Must be computer literate.
Ability to establish and maintain effective working relationships with coworkers, managers and clients.

Join Us

Making a positive impact on human health takes insight, curiosity, and intellectual courage. It takes brave minds, pushing the boundaries to transform healthcare. Regardless of your role, you will have the opportunity to play an important part in helping our clients drive healthcare forward and ultimately improve outcomes for patients.

Forge a career with greater purpose, make an impact, and never stop learning.

Job ID:R1129461

Source: Careesma



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