Job Description

Years of Experience: 9 to 12 yearsSkill Set / Exposure: PV background, DSUR, PBRER, Addendum to CO, PADER/PAER and Risk Management Plans.:

• The Principal Medical Writer is an individual expert contributor capable of independently executing complex writing assignments involving a thorough understanding of safety documents (e.g., aggregate reports and Risk Management Plans [RMPs]) and interpretation of safety data.
• They must demonstrate the ability to independently manage the production of safety deliverables, including those involving complex data analyses or important safety issues.
• This role requires extensive safety document expertise and will support continuous improvement and the implementation of best practices and adoption of new tools and technology.

Key Responsibilities:

• Independently lead preparation of complex clinical and post-market safety documents, including but not limited to Development Safety Update Reports (DSURs), Periodic Safety Update Reports/Periodic Benefit-Risk Evaluation Reports (PSURs/PBRERs), Addendums to Clinical Overviews (ACOs), US Periodic Adverse Drug Experience Reports/Periodic Adverse Experience Reports (PADERs/PAERs), RMPs and responses to regulatory authority questions.
• Provide oversight to co-authors or team of writers as applicable and be accountable for the quality of their work/contributions.
• Lead cross-functional teams in document preparation including but not limited to development of content strategy, coordination of content contributions, organization of review schedules, and project timelines.
• Work in a matrix team to ensure delivery of high-quality, fit-for-purpose documents that reflect accurate interpretation of associated safety, clinical, and statistical data, and are in line with GSK standards and global, regional, and/or local regulatory requirements.
• Understand the interdependencies of various contributing functions (e.g., safety, regulatory, clinical, epidemiology, statistics, and programming).
• Anticipate and evaluate complex situations and problems, resolving them by leveraging scientific and operational knowledge in collaboration with stakeholders.
• Assess trends and patterns in text and statistical data and effectively organize content and messages in safety documents.
• Use approaches to expedite document preparation, including authoring and reviewing tools, as well as other automation/technology platforms.
• Serve as a mentor for less experienced writers.
• Develop and deliver training on medical writing topics.
• Lead initiatives to improve medical writing processes.
• Contribute to vendor oversight as needed.

Education Requirements:

• Masters degree or equivalent in a scientific discipline.
• A degree in Medicine/Dentistry/Physiotherapy/Experimental Medicine, which involves patient exposure in a hospital-based environment, would be an advantage.

Job Related Experience:

• Minimum of 7 years of advanced safety writing experience in the pharmaceutical domain including summarization and interpretation of complex data and preparation of complex documents.

In depth working knowledge of:

• Relevant regulatory guidance (e.g., ICH, GVP, FDA, EMA) pertaining to clinical trial conduct, pharmacovigilance, and document-specific requirements.
• Core cross-functional clinical research roles and procedures, and how they relate to document strategy and operational preparation.
• Experience in multiple therapeutic areas to have confidence to dive into these areas without lead time.
• Advanced understanding of and ability to apply the statistical, regulatory, and medical communication concepts needed to independently write complex safety documents.

Other Job-Related Skills:

• Advanced safety writing skills with expertise in most safety document types.
• Highly collaborative, capable of leading crossxe2x80x90functional team members, negotiating solutions, and advising them on document structure and content as needed.
• Skilled in navigating multicultural settings, ensuring effective collaboration with diverse customers and clients, such as health authorities and patients, while adeptly collaborating with remote teams.
• Able to independently lead multiple projects simultaneously and deliver multiple high-quality documents on schedule.
• Advanced computer skills and general computer literacy.
• Excellent English language proficiency, both verbal and written.

Inclusion at GSK:

• As an employer committed to Inclusion, we encourage you to reach out if you need any adjustments during the recruitment process.
• Please contact our Recruitment Team at IN.recruitment-adjustments@gsk.com to discuss your needs.

Why GSK?Uniting science, technology and talent to get ahead of disease together.GSK is a global biopharma company with a special purpose to unite science, technology and talent to get ahead of disease together so we can positively impact the health of billions of people and deliver stronger, more sustainable shareholder returns as an organisation where people can thrive. We prevent and treat disease with vaccines, specialty and general medicines. We focus on the science of the immune system and the use of new platform and data technologies, investing in four core therapeutic areas (infectious diseases, HIV, respiratory/ immunology and oncology).Our success absolutely depends on our people. While getting ahead of disease together is about our ambition for patients and shareholders, its also about making GSK a place where people can thrive. We want GSK to be a place where people feel inspired, encouraged and challenged to be the best they can be. A place where they can be themselves feeling welcome, valued, and included. Where they can keep growing and look after their wellbeing. So, if you share our ambition, join us at this exciting moment in our journey to get Ahead Together.Important notice to Employment businesses/ AgenciesGSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK's commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site.It has come to our attention that the names of GlaxoSmithKline or GSK or our group companies are being used in connection with bogus job advertisements or through unsolicited emails asking candidates to make some payments for recruitment opportunities and interview. Please be advised that such advertisements and emails are not connected with the GlaxoSmithKline group in any way.GlaxoSmithKline does not charge any fee whatsoever for recruitment process. Please do not make payments to any individuals / entities in connection with recruitment with any GlaxoSmithKline (or GSK) group company at any worldwide location. Even if they claim that the money is refundable.If you come across unsolicited email from email addresses not ending in gsk.com or job advertisements which state that you should contact an email address that does not end in gsk.com, you should disregard the same and inform us by emailing askus@gsk.com, so that we can confirm to you if the job is genuine.

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