Open role
Biomarker Studies Asset Manager
- Aggregated by CV-Library
- Welwyn Garden City, Hertfordshire
- Contract
- Full Time
- £164,250 - £182,500 Per Day
Job Description
Join Our Team as a Contractor Biomarker Studies Asset Manager (BSAM)!
Are you ready to make a meaningful impact in the pharmaceutical industry? Our client is seeking a dynamic Biomarker Studies Asset Manager to lead the charge in biomarker operational study management. This is a fantastic opportunity to contribute to transformative drug development while working in a collaborative and innovative environment.
About the Role:
As a Biomarker Studies Asset Manager, you will play a crucial role in ensuring the successful planning and execution of biomarker strategies for clinical studies. Your expertise will drive efficiency and quality in biomarker operations, making a difference in the lives of patients worldwide.
Key Responsibilities:
Operational Management: Oversee end-to-end biomarker operations activities, ensuring quality data input and delivery for both clinical and investigational device studies.
Protocol Development: Contribute to the creation of protocols, informed consent forms (ICFs), and Biomarker Management Plans (BMP).
Vendor Management: Manage activities of central laboratories and specialty biomarker labs/vendors, focusing on project scope, budget, and timelines.
Cross-Functional Collaboration: Partner with various teams to coordinate biomarker data requirements and ensure timely delivery of results.
Technical Expertise: Provide insights into biomarker analyses, including sample collection, assay techniques, and imaging technologies.
Regulatory Compliance: Ensure adherence to ICH/GCP, SOPs, ISO standards, and other regulatory requirements.What You Bring:
Experience: Clinical research/operations role, with a focus on clinical/diagnostic development or pharmaceutical R&D.
Education: A university degree in life sciences or equivalent experience.
Project Management Skills: Strong experience in vendor and project management.
Regulatory Knowledge: Familiarity with drug development processes and relevant regulations.
Communication Skills: Excellent collaboration, communication, and presentation abilities.
Growth Mindset: A passion for learning and innovating in fast-paced, collaborative environments.Why Join Us?
Temporary Position: This is a 6-month contract that offers you the chance to make a significant impact.
Exciting Work Environment: Work alongside passionate professionals dedicated to transforming drug development.
Flexible Work Arrangement: Enjoy the autonomy of a contractor role while contributing to meaningful projects.If you're a self-starter with a keen eye for detail, a knack for problem-solving, and a desire to innovate, we want to hear from you! This is your chance to be part of something bigger - a mission to deliver transformative medicines by 2029.
We look forward to your application!
Adecco is a disability-confident employer. It is important to us that we run an inclusive and accessible recruitment process to support candidates of all backgrounds and all abilities to apply. Adecco is committed to building a supportive environment for you to explore the next steps in your career. If you require reasonable adjustments at any stage, please let us know and we will be happy to support you.
We use generative AI tools to support our candidate screening process. This helps us ensure a fair, consistent, and efficient experience for all applicants. Rest assured, all final decisions are made by our hiring team, and your application will be reviewed with care and attention
Are you ready to make a meaningful impact in the pharmaceutical industry? Our client is seeking a dynamic Biomarker Studies Asset Manager to lead the charge in biomarker operational study management. This is a fantastic opportunity to contribute to transformative drug development while working in a collaborative and innovative environment.
About the Role:
As a Biomarker Studies Asset Manager, you will play a crucial role in ensuring the successful planning and execution of biomarker strategies for clinical studies. Your expertise will drive efficiency and quality in biomarker operations, making a difference in the lives of patients worldwide.
Key Responsibilities:
Operational Management: Oversee end-to-end biomarker operations activities, ensuring quality data input and delivery for both clinical and investigational device studies.
Protocol Development: Contribute to the creation of protocols, informed consent forms (ICFs), and Biomarker Management Plans (BMP).
Vendor Management: Manage activities of central laboratories and specialty biomarker labs/vendors, focusing on project scope, budget, and timelines.
Cross-Functional Collaboration: Partner with various teams to coordinate biomarker data requirements and ensure timely delivery of results.
Technical Expertise: Provide insights into biomarker analyses, including sample collection, assay techniques, and imaging technologies.
Regulatory Compliance: Ensure adherence to ICH/GCP, SOPs, ISO standards, and other regulatory requirements.What You Bring:
Experience: Clinical research/operations role, with a focus on clinical/diagnostic development or pharmaceutical R&D.
Education: A university degree in life sciences or equivalent experience.
Project Management Skills: Strong experience in vendor and project management.
Regulatory Knowledge: Familiarity with drug development processes and relevant regulations.
Communication Skills: Excellent collaboration, communication, and presentation abilities.
Growth Mindset: A passion for learning and innovating in fast-paced, collaborative environments.Why Join Us?
Temporary Position: This is a 6-month contract that offers you the chance to make a significant impact.
Exciting Work Environment: Work alongside passionate professionals dedicated to transforming drug development.
Flexible Work Arrangement: Enjoy the autonomy of a contractor role while contributing to meaningful projects.If you're a self-starter with a keen eye for detail, a knack for problem-solving, and a desire to innovate, we want to hear from you! This is your chance to be part of something bigger - a mission to deliver transformative medicines by 2029.
We look forward to your application!
Adecco is a disability-confident employer. It is important to us that we run an inclusive and accessible recruitment process to support candidates of all backgrounds and all abilities to apply. Adecco is committed to building a supportive environment for you to explore the next steps in your career. If you require reasonable adjustments at any stage, please let us know and we will be happy to support you.
We use generative AI tools to support our candidate screening process. This helps us ensure a fair, consistent, and efficient experience for all applicants. Rest assured, all final decisions are made by our hiring team, and your application will be reviewed with care and attention