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Associate Director, Statistical Programming
Grifols Worldwide Op Ltd —Dublin, County Dublin
The duties and responsibilities include, but are not limited to, the following: Drives standardization within the Biometry group, innovating to develop…
Associate Director, Translational Medicine
Grifols Worldwide Op Ltd —Dublin, County Dublin
Wellness and social initiatives, including activities such as padel and summer events. Depending on the area ofassignment,directly related experience or a…

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Associate Director, Translational Medicine

Grifols Worldwide Op Ltd -
Dublin, County Dublin

Apply Now

Job details

Full-time

Benefits

Private medical insurance

Qualifications

Biology
Biochemistry
Doctoral degree
Master's degree
Project management
Bachelor's degree
Communication skills

Full job description

Would you like to join an international team working to improve the future of healthcare? Do you want to enhance the lives of millions of people? Grifols is a global healthcare company that since 1909 has been working to improve the health and well-being of people around the world. We are leaders in plasma-derived medicines and transfusion medicine and develop, produce and market innovative medicines, solutions and services in more than 110 countries and regions.

At Grifols, we believe that diversity adds value to our business, our teams, and our culture. We are committed to equal employment opportunities that foster an inclusive environment.

POSITION SUMMARY:

The Associate Director of Translational Medicine bridges drug discovery (by application of preclinical studies) to clinical programs. The key roles of this position are to
define translational strategies, manage external partners and ensure scientific rigor for decision making in drug development. The Associate Director of Translational
Medicine focuses on biomarker discovery, assay development and clinical trial support by working closely with the discovery, pharmacology, clinical development and
regulatory teams to advance therapeutic programs.

What You Will Do:

Develop and implement scientific strategy of translational medicine studies, interpret data to support of program objectives.
Discover, validate, and implement biomarkers to assess drug response, understand mechanism of action, and biomarker measures for animal and patient studies
Prepare IND supporting documentation and participate in pre-IND meetings with regulatory authorities.
Defines and executes strategic plans for translational science projects that are aligned with regulatory expectations.
Manage external partners like Contract Research Organizations (CROs) to ensure high quality and timely study execution.
Initiate new areas of investigation and implement cutting-edge technologies that are scientifically meaningful, reliable and can be incorporated directly into both preclinical and clinical development programs
Present scientific findings internally and externally.
Designs investigative translational strategies in support of research, preclinical and clinical development as well as regulatory strategies
Leads the planning and implementation of experimental programs, with internal (Grifols) or external stakeholders, in support of asset readiness for clinical development phase
Directs and coordinates experimental programs, with internal (Grifols) or external stakeholders, in support of asset readiness for clinical development phase
Interprets, synthesizes and communicates preclinical and clinical biomarker study results to support key program decision making
Provides scientific, technological and strategic guidance to biomarker and/or bioanalytical programs accompanying clinical trials in collaboration with nonclinical and clinical teams
Contributes to the creation of study-level documents, including review/ preparation of non-clinical sections of key regulatory documents, such as protocols, Investigator’s Brochures,briefing meeting request & package and submission dossiers.
May participate in due diligence assessments of potential external assets and participate and ISR evaluations
May represent Grifols at external functions such as conferences
May manage a team of scientists and research associates
rives TM program evaluations within a multifunctional team and presents business opportunities the Senior Management.
Works closely with Quality Management & Assurance to ensure work conducted by qualified vendors
Assesses/implements departmental standardizations for new and improved practices and or consistent work practices, and SOPs
Serve as a subjectmatter expert providing scientific guidance and support to project teams
Provides translational teams leadership and develops teams with technical depth
Contributes to developing and executing work in support of corporate goals
Developing and managing vendor budgets

What You’ll Bring

Excellent knowledge of relevant diseases and biological processes
Excellent and demonstrated project management skills. Excellent oral and written communication skills.
Communicates complex technical and business information to technical and/or non-technical audiences as well as upper management.
Ability to interpret data, identify errors and provide corrective actions to procedures and processes to generate valid conclusions.
Expertise in setting and meeting deadlines, multitasking, as well as identifying, requesting and prioritizing team resources based on project needs.
Ability to anticipate future change and recommends strategies for optimizing processes and procedures that will mitigate long-term foreseeable problems
Demonstratable deep knowledge ofrelated field principles, tools, and/or databases
Adaptability to change in priorities
Consistently motivated, even under difficult situations
Excellent team player that creates an atmosphere for collaborative effort among the team
Ability to articulate strategic options and scenarios to inform operational delivery of the project(s), understanding how to focus on the delivery of goals and contributes strategic insights to prioritization and decision-making.
Makes solid decisions based on a combination ofanalysis, experience and professional judgement.
PhD orMSin Biology,Biochemistry, Immunology, Biological Engineering or related field.
5-8 years of related experience.
Depending on the area ofassignment,directly related experience or a combination of directly related education and experience and/or competencies may be considered in place of the stated requirements. Example: If a job level requires a Bachelor’s degree plus 4 years of experience, an equivalency could include 8 years of experience, an
Associate’s degree with 6 years of experience, or a Master’s degree with 2 years of experience.

Our Benefits Include:

A highly competitive salary package
Group pension scheme - Contribution rates are (3%/ 5%/ 7%) and company will match
Private medical insurance for the employee
Ongoing career development opportunities within a rapidly growing organisation
Strong focus on succession planning and internal promotion
Dedicated education and professional development allowance
Wellness and social initiatives, including activities such as padel and summer events
Mostly remote working model ( in Ireland) , supporting work–life balance

We understand that self-doubt can hold talented individuals back from applying for opportunities. We encourage everyone who meets the qualifications to apply – we're excited to hear from you

#LI-FD1

Location: Grange Castle International Business Park, Grange, Co. Dublin, D22 K2R3

Learn more about Grifols

Apply Now

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study director/project jobs

Associate Director, Translational Medicine

Associate Director, Statistical Programming

Senior Mechanical Engineer

Senior Associate - Tax (Customs Team)

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Senior Speech & Language Therapist in Older Persons

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