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Medical Writing Asset Lead (Associate Director)

Brentford

Job Type

Job Function

Medical and Clinical

Location

Brentford

On-Site or Remote

Job Type

Salary

Competitive salary and benefits

About the Role

*Job description* *Site Name:* Warsaw, Canada - Ontario - Mississauga, India - Karnataka - Bengaluru, UK - London - Brentford *Posted Date:* Jan 15 2024 *Associate Director Medical Writing Asset Lead* Are you energized by a medical writing role that allows you to shape operational strategy and accelerate product approvals? If so, this Associate Director Medical Writing Asset Lead role could be an exciting opportunity to consider. As an Associate Director Medical Writing Asset Lead, you will implement operational strategy guided by the Therapeutic Area Head of Medical Writing, tracking milestones and deliverables to manage the performance of the Medical Writing team, ensuring consistency, regulatory compliance, and high quality of functional deliverables. You will apply experience, scientific and operational expertise, and leadership in a matrix organization to provide Medical Writing strategy to one or more therapeutic area assets, to design and deliver high-quality fit for purpose clinical documents including those for regulatory submissions, to plan for efficient and accelerated ways of working, and to contribute to key organizational process improvements. This is a highly visible medical writing role, that will provide YOU the opportunity to lead key activities to progress YOUR career. *Leadership and Expertise :* - Lead one or more drug and/or vaccine assets and serve as a medical writing point of contact for this/these assets. - Provide the medical writing strategy for the development of clinical programs and content of documents. - Lead matrix team to deliver high quality, fit-for-purpose clinical documents that accurately reflect associated data and are in line with GSK standards and global/regional/local regulatory requirements. - Clinical documents in scope include clinical study protocols, clinical study reports, briefing documents for regulatory authorities, responses to regulatory authority questions, clinical sections of the IMPD/IND for clinical trial applications, investigator brochures, annual reports, Common Technical Document Summaries and Clinical Overview. - Collaborate with in house, CROs and/or independent contractor medical writers to ensure on-time delivery of high-quality fit for purpose documents. Collaborate closely with Global Regulatory Affairs and other cross-functional groups to understand business needs and clinical data. - Demonstrate high performance standards for own work and encourage similar standards across the matrix team. - Ensure Medical Writing strategy is aligned with the portfolio strategy (e.g., prioritization, acceleration, meeting upper quartile performance). Provide guidance and facilitation to submission teams in development of submission plans. Recommend solutions for problems that affect timelines. - Drive, promote and implement key organizational process improvement initiatives. Proactively generate ideas for simplification and improvement taking advantage of opportunities that arise. Promote environment for others to generate ideas for improvement (e.g., continuously challenge the status quo) and champion novel business solutions in technology and ways of working. - Lead development of training materials for a range of clinical documents. Provide mentoring, coaching and/or training to individuals or teams to develop others and share learnings. - Promote leadership behaviors that support GSK values.Provide resourcing information to Medical Writing Therapeutic Area Head to contribute to budget forecast, escalate risks and opportunities to ensure optimal resource utilization and timely product approvals. *Matrix Teamwork and Function:* - Establish quality, efficiency, and effective teamwork across all clinical document teams. - Work closely with stakeholders to provide significant contribution to complex clinical submission documents, document strategy and on time, efficient document delivery. *Relationship, Influence and Communication:* - Lead and influence teams in a matrix environment. Promote team effectiveness across assigned projects. Build and maintain networks at project, departmental and inter-departmental levels. Ensure timely dissemination of information to appropriate levels to ensure transparency and shared learnings. - Ensure effective communication, including clear presentation of ideas and data to a group, which may include key stakeholders at senior level or external opinion leaders. - Influence and advocate for medical writers, team members and senior stakeholders to effectively contribute to and review documents. - Support a culture of open and honest conversations, smart risk taking, decision-making, and pushing the performance edge within Medical Writing and in cross-functional platforms. - Be pragmatic with strong negotiation skills (to propose creative solutions to new challenges) - Continually engage stakeholder departments, work with stakeholder departments to identify risks and opportunities, and socialize new initiatives (e.g., new templates and processes) *Planning, Organization and Team Coordination:* - Able to develop and implement study and above study document and resourcing strategies to meet project team objectives and anticipated deliverables. - Able to develop a resourcing plan to enable efficient and accelerated delivery of documents and submissions. - Flexibility to adjust plans when project timings change. *Process Improvement and Compliance:* - Support process improvement, training, quality and compliance through ideas, proactive action, and engagement in the matrix team. *Additional Job Responsibilities:* - Identify risks to strategic, ethical or compliance objectives (e.g., article 46 compliance or delivery of a critical-path documents needed to deliver our pipeline) and put in place appropriate mitigation strategies. - Measure and monitor efficiency, quality (incl. consistency) and scientific integrity of writing. - Ensure good writing practices and fluid communication within study teams. - Ensure appropriate leadership/ownership of writers on the clinical project teams to enable the optimal planning and delivery of documents (esp. for producing critical documents). - Drive thorough submission planning and delivery with application of agile, efficient and accelerated processes as needed. - Resource management *Why you?* *Basic Qualifications:* We are looking for professionals with these required skills to achieve our goals: - PhD, PharmD, MPH, MSc, or other post-graduate degree. - Proven track record in writing clinical documents in scope. - 6+ years’ experience in clinical regulatory writing in the pharmaceutical industry - 6+ years’ experience in project management, planning, communication, and matrix leadership - 6+ years’ experience working with International Council for Harmonization (ICH)/Good Clinical Practice (GCP) Guidelines *Preferred Qualifications:* If you have the following characteristics, it would be a plus: - Highly effective communication skills and capability to present ideas and data clearly to a group, including key stakeholders at senior level. - Demonstrated track record of quality decision making and creative problem resolution that impacts program/project direction. - Experience analyzing complex scientific & operational information and implementing effective solutions. - Experience in Risk Management and Management Monitoring - Effective ability to prioritize tasks and deliver on deadlines. - Proven track record of successfully managing simple to medium complex programs. *At GSK we offer a wide range of additional benefits: * - Career at one of the leading global healthcare companies. - Contract of employment. - Car or car allowance - Attractive reward package (annual bonus & awards for outstanding performance, recognition awards for additional achievements and engagement, holiday benefit). - Extensive support of work life balance (flexible working solutions, min. 2 days/week working form the office, short Friday’s option, health & well-being activities). - Life insurance and pension plan. - Private medical package with additional preventive healthcare services for employees and their eligible. - Sports cards (Multisport). - Possibilities of development within the role and company’s structure. - Personalized learning approach (internal trainings, mentoring, access to online training’ platforms: Keep Growing Campus, LinkedIn Learning, Business Skills, Harvard Manage Mentor, Skillsoft and external training). - Supportive community and integration events. - Modern office with creative rooms, fresh fruits every day. #LI-GSK #LI-HYBRID *Why Us?* 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 organization where people can thrive. Getting ahead means preventing disease as well as treating it, and we aim to positively impact the health of 2.5 billion people by the end of 2030. Our success absolutely depends on our people. While getting ahead of disease together is about our ambition for patients and shareholders, it’s also about making GSK a place where people can thrive. We want GSK to be a workplace where everyone can feel a sense of belonging and thrive as set out in our Equal and Inclusive Treatment of Employees policy. We’re committed to being more proactive at all levels so that our workforce reflects the communities we work and hire in, and our GSK leadership reflects our GSK workforce. If you require an accommodation or other assistance to apply for a job at GSK, please contact the GSK Service Centre at 1-877-694-7547 (US Toll Free) or +1 801 567 5155 (outside US). GSK is an Equal Opportunity/Affirmative Action Employer. All qualified applicants will receive equal consideration for employment without regard to race, color, national origin, religion, sex, pregnancy, marital status, sexual orientation, gender identity/expression, age, disability, genetic information, military service, covered/protected veteran status or any other federal, state or local protected class. *Important notice to Employment businesses/ Agencies* GSK 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. Please note that if you are a US Licensed Healthcare Professional or Healthcare Professional as defined by the laws of the state issuing your license, GSK may be required to capture and report expenses GSK incurs, on your behalf, in the event you are afforded an interview for employment. This capture of applicable transfers of value is necessary to ensure GSK’s compliance to all federal and state US Transparency requirements. For more information, please visit GSK’s Transparency Reporting For the Record site.

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