Are you interested in developing and commercializing safer and more effective supportive care agents and therapeutics? If so, the Regulatory Project Manger- CMC Technical Writing position might be for you.
As Regulatory Project Manger- CMC Technical Writing, you will ensure that GSK is executing regulatory strategies and supporting interactions with regulatory authorities appropriately.
This role will provide YOU the opportunity to lead key activities to progress YOUR career, these responsibilities include some of the following…
Develop and lead the execution of submission plans. Consult on and be accountable for the execution of timely and innovative regulatory strategies in support of global development and life cycle management of assigned projects
Collaborate with Global RA CMC lead and/or Regional RA CMC lead to provide regulatory support for assigned projects
Contribute to the evaluation of the impact of changes to the regulatory landscape
Collaborate with Regulatory Operations for the preparation of global clinical trial applications, marketing applications and post-approval supplements and variations
Contribute strategically to the development of and to the definition of the CMC content requirements for timely approval of regulatory filings throughout the product life cycle (IND, IMPD, BLA, MAA)
Plan and manage resource needs for authoring, review and approval of submission-ready documents for a projects
Ensure submissions are complete and accurate, and comply with applicable regulatory requirements and expectations
Review submission documents to ensure messaging and content is clear and consistent within and across documents
Work collaboratively with RA CMC colleagues and SMEs to interpret and summarize complex data into CMC documents intended for submissions to Global Health Authorities using templates and style guide.
We are looking for professionals with these required skills to achieve our goals:
BA/BS in scientific or technical discipline
At least 5+ years of biopharmaceutical regulatory experience
Experience preparing CMC sections of INDs, IMPDs, BLAs, MAAs, and supportive amendments and supplements (ICH Modules 2 and/or 3)
Project management experience
If you have the following characteristics, it would be a plus:
Thorough understanding of the drug development process for all phases of pharmaceutical development and applied comprehensive understanding of regulations and guidelines to enhance probability of regulatory success and regulatory compliance
Thorough understanding of FDA regulations and ICH guidance pertaining to pharmaceutical development of NME targets and marketed products
Exposure to regulatory requirements for biologic product development is highly desired
Proven ability to work with a high level of integrity, accuracy, and attention to detail
Strong problem-solving skills to evaluate technical information and identify appropriate regulatory actions with limited supervision
Self-motivated, assertive, and self-confident with the ability to act with a sense of urgency and passion
Strong organizational skills in order to maintain a high level of productivity, innovation, and a sense of urgency to ensure assignments are completed on-time and on-budget with a high level of quality
Ability to make timely and meaningful decisions and take corresponding actions
Willingness to work collaboratively by incorporating diverse perspectives and in order to strengthen decision-making
Proactively identifies and implements process improvements
Proven ability to manage multiple projects, identify and resolve regulatory issues
Ability to balance regulatory objectives with business objectives
Ability to influence the regulatory team in a positive way
Ability to take disparate inputs and drive them into one cohesive strategic regulatory decision
Excellent oral and written communication skills for effectively interfacing with all levels of management and departments within the company
Resourceful, creative, enthusiastic, and results-oriented
Strong interpersonal skills and the ability to effectively work with other departments and vendors
Positive and energetic attitude
Our values and expectations are at the heart of everything we do and form an important part of our culture. These include Patient focus, Transparency, Respect, Integrity along with Courage, Accountability, Development, and Teamwork. As GSK focuses on our values and expectations and a culture of innovation, performance, and trust, the successful candidate will demonstrate the following capabilities:
Operating at pace and agile decision-making – using evidence and applying judgement to balance pace, rigour and risk.
Committed to delivering high quality results, overcoming challenges, focusing on what matters, execution.
Continuously looking for opportunities to learn, build skills and share learning.
Sustaining energy and well-being.
Building strong relationships and collaboration, honest and open conversations.
Budgeting and cost-consciousness.
Internal Number: 255683
We are a science-led global healthcare company with a special purpose: to help people do more, feel better, live longer.
We have three global businesses that research, develop and manufacture innovative pharmaceutical medicines, vaccines and consumer healthcare products. Every day, we help improve the health of millions of people around the world.
Our goal is to be one of the world’s most innovative, best performing and trusted healthcare companies.
Our values and expectations are at the heart of everything we do - so that together we can deliver extraordinary impact for our patients and consumers and make GSK a brilliant place to work.
Our values are Patient focus, Transparency, Respect, Integrity.
Our expectations are Courage, Accountability, Development, Teamwork.