Senior Regulatory Affairs Specialist
Location: NetherlandsSIRE® is the market leader in Life Sciences recruitment. We believe the recruitment market needs to gear up in technology and continuous innovation. We like technology, in a Life Sciences market driven on science, we couldn’t stay behind; we drive Recruitment Science. Investing a majority of our turnover in technology enables us to use unique Resource Technologies. By using highly advanced algorithms, we enable our team of Resource & Data Strategists© to maintain the most advanced, detailed and complete Life Sciences network in Europe. This big data enables us to work Reverse Recruitment©: we first analyze the market in-depth before we go out to the market. Because we analyze the whole market, we can compare facts and data. This enables us to do Facts & Big Data Recruitment©, making sure we, or better yet, you find the right career!Our client is a professional Pharmaceutical organisation, based in Zuid-Holland Netherlands.
Authors/drives, as appropriate, sections of the CMC dossier and evaluates/ensures that final versions comply with regulatory requirements and fulfill regulatory agency expectations with some managerial guidance. The Senior Scientist supports the technical functions in the development of responses to health authority inquiries in support of clinical trials as well as marketing applications with some managerial guidance. Evaluates and ensures the completeness, accuracy, and compliance of data provided for all regulatory submissions with some managerial guidance. Ensures all Quality submissions are completed in a timely manner.
- Executes dossier strategy / product development plan with a high level of autonomy
- Direct responsibility for project budgets
- May lead dossier authoring activities for late stage projects for regulatory filings with some managerial support
- Identifies business improvement areas and, under some managerial supervision, drives implementation of improvements
- Develops process and business improvements within own functional organization, and aligns with other departments as needed
- With some guidance, interfaces directly with CMC/Tech team members, Regulatory, JSC, external service providers and internal PDMS customers such as GCO and TA.
- Interfaces mainly internal functional stakeholders, some external stakeholders
- Influences or persuades others to accept new ideas, approaches or concepts or gains alignment on divergent issues with some guidance
- Combines technical expertise with management skills. May manage a consultant
- Manages limited number of projects with standard, rather than accelerated priority, or with assistance of a Senior staff member, manages complex projects with potentially accelerated priority
- Challenges status quo and has ability to identify innovative approaches to improve products/processes
- Scope is primarily incremental innovation, within own dept / team.
- With guidance, resolves cross-functional issues
- Appropriately identifies and manages key stakeholders, and escalates when needed to obtain senior management support. With some guidance, takes day-to-day decisions on operational priorities for his/her team, and allocates resources accordingly
- Works mostly independently on a day to day basis, checks in with supervisor weekly
- Manages functional or project teams with up to 10 members
OR University degree with 6+ years relevant experience OR Equivalent by experience
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Rowin van der Zwaan.
Role Description
The Senior Scientist, Dossier Development, PDMS is responsible, with some managerial guidance, for developing the technical eCTD sections to support Regulatory CMC dossier applications. With some managerial guidance, coordinates and provides technical oversight for the generation of the CMC dossier of marketing and clinical trial submissions. Coordinates the timeline, virtual document, and generation of the Quality module. Assumes personal ownership and accountability for business results and solutions, working with some managerial supervision. Represents the department on multi-functional project development teams to support regulatory filings.Authors/drives, as appropriate, sections of the CMC dossier and evaluates/ensures that final versions comply with regulatory requirements and fulfill regulatory agency expectations with some managerial guidance. The Senior Scientist supports the technical functions in the development of responses to health authority inquiries in support of clinical trials as well as marketing applications with some managerial guidance. Evaluates and ensures the completeness, accuracy, and compliance of data provided for all regulatory submissions with some managerial guidance. Ensures all Quality submissions are completed in a timely manner.
Responsibilities
- Supports dossier strategy / product development plan creation at a compound level- Executes dossier strategy / product development plan with a high level of autonomy
- Direct responsibility for project budgets
- May lead dossier authoring activities for late stage projects for regulatory filings with some managerial support
- Identifies business improvement areas and, under some managerial supervision, drives implementation of improvements
- Develops process and business improvements within own functional organization, and aligns with other departments as needed
- With some guidance, interfaces directly with CMC/Tech team members, Regulatory, JSC, external service providers and internal PDMS customers such as GCO and TA.
- Interfaces mainly internal functional stakeholders, some external stakeholders
- Influences or persuades others to accept new ideas, approaches or concepts or gains alignment on divergent issues with some guidance
- Combines technical expertise with management skills. May manage a consultant
- Manages limited number of projects with standard, rather than accelerated priority, or with assistance of a Senior staff member, manages complex projects with potentially accelerated priority
- Challenges status quo and has ability to identify innovative approaches to improve products/processes
- Scope is primarily incremental innovation, within own dept / team.
- With guidance, resolves cross-functional issues
- Appropriately identifies and manages key stakeholders, and escalates when needed to obtain senior management support. With some guidance, takes day-to-day decisions on operational priorities for his/her team, and allocates resources accordingly
- Works mostly independently on a day to day basis, checks in with supervisor weekly
- Manages functional or project teams with up to 10 members
Requirements
PhD with Post-doc experience with 3+ years relevant experienceOR University degree with 6+ years relevant experience OR Equivalent by experience
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Rowin van der Zwaan.
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