Senior Medical Writer Job Vacancy in Parexel Bengaluru, Karnataka – Latest Jobs in Bengaluru, Karnataka

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Company Name : Parexel
Location : Bengaluru, Karnataka
Position : Senior Medical Writer

Job Description : Parexel’s Regulatory Medical Writing Services works closely with our clients around the world to develop and launch new medicines and treatments that improve healthcare for millions of patients. We’re one of the largest providers of medical writing services worldwide, and have managed thousands of writing projects in more than 29 countries across North and South America, Europe, Asia, and Africa. As a result of continued customer satisfaction and business growth, this global team is expanding and offers many opportunities for career development.
In this role, you’ll prepare clinical documents for comprehensive clinical trials and programs. Using compliant Parexel and sponsor formats, styles and management systems, you’ll manage clinical document deliverables such as model informed consent forms, clinical study reports, pharmacovigilance documents and more. Our Medical Writers also participate in ongoing professional development programs to maintain current knowledge in the various areas. Explore opportunities within our core Clinical Development, Biotech, or Functional Service Provider (FSP) teams below.
Full Time
Travel: No
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Detail-Oriented
Deadline-Oriented
Communicator
Organized
Versatile
Tech-Savvy
Rewards
Global Impact
We are one truly global team working together to propel each client´s journey ahead faster.
Work-life Balance
We value work-life balance. We try and keep regular hours and an emphasis on life outside the office.
Career Development
Opportunity to learn and grow through a performance and development goal-setting program.
Home based
Love where you work, and work where you love.
Variety
Opportunity to work on a wide range of therapeutic areas, document types and clinical projects.
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, safety update/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.
Follow required standard operating procedures (SOPs), templates, guidelines,
regulations, client instructions and other processes, as applicable.
Perform literature searches/reviews as necessary to obtain
background information and training for development of documents.
Review statistical analysis plans and mock statistical output to
determine appropriateness of content at for clinical writing.
Ensure that all work is complete and of high quality prior to team distribution or
shipment to client.
o Confirm data consistency and integrity across the document.
o Prepare documents for publishing readiness, when applicable.
o Ensure document structure, content, and style adheres to FDA/EMA or other appropriate regulatory guidelines, and comply with departmental,
corporate or client SOPs and style guidelines, as applicable.
o Provide suggested alternative content when contributors provide content
that does not meet document needs.
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.
Act in the capacity of project manager/lead for medical writing projects, which
may entail serving as the primary client contact, negotiating deliverable
timelines, and resolving project-related issues. Project management of contractual and financial aspects may only be performed with the guidance of medical writing management.
Serve as the Medical Writing representative on assigned project teams and
demonstrate document leadership: communicate content requirements, coordinate and conduct interdepartmental team review of draft and final documents, schedule and lead/facilitate authoring team meetings to agree on expectations, evaluate progress on tasks, identify issues and facilitate resolutions, manage/drive the timeline, and advance document development to approval, according to Parexel or client guidelines/SOPs. Distribute final documents to project team and client.
Identify any potential project challenges to departmental line management
and project leader, including changes in project plan, timeline or out of scope
requests, and suggest possible resolution options.
Attend or lead project team meetings as required. Mediate conflict or
disagreement, as well as timeline delays, among team members by
negotiating, compromising, and facilitating open exchange of ideas
and opinions to come to a consensus.
Supervise collection of documentation by Medical Writing Support Coordinator,
Document Specialist, and/or Associate Medical Writer for assembly of project
files and client deliverables. Ensure appropriate filing of project documentation with assistance from the Medical Writing Support Coordinator.
Build and maintain collaborative relationships with teams/clients for
an efficient, productive, and professional working relationship.
Qualifications
Excellent interpersonal, verbal, and written communication skills.
Ability to consistently produce documents of high quality.Demonstrates attention to details and proactivity.Ability to understand all necessary steps in a project, plan ahead, and identify critical paths.
• A flexible attitude with respect to work assignments and new learning; readily adapts to changes. • Ability to efficiently manage time spent on tasks and proactively identify deficiency. Manage
multiple and varied tasks with enthusiasm and prioritize workload with attention to detail, e.g.,
organizational skills.
Competent working in a matrix environment and values the importance of teamwork. Possesses
team leadership skills and cross-cultural sensitivity.
Ability to negotiate on behalf of medical writing to ensure resources, timelines and
expectations are aligned.
Understands and satisfies client needs.Gains trust and establish a connection with the client beyond one’s project, to gain
repeat business and/or to widen existing scope and services.
Provides departmental expertise and perspectives to promote prospective business
opportunities; provide Parexel colleagues with pertinent information to formalize a sound business strategy.
Demonstrated understanding of clinical research, the drug development process, and industry
guidelines and regulations, e.g., ICH-GCP.
Extensive clinical/scientific writing skills.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.
If required to perform translation work and quality control of documents written in non-English
language, proficiency in relevant language is a prerequisite.
Bachelor’s degree in Life Sciences/Health Related Sciences or equivalent.

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