The Senior Director serves as the regulatory lead for relevant product program teams and will manage other members of the regulatory affairs organization. This includes supporting the VP of Regulatory Affairs in ensuring the development, implementation and alignment of regulatory strategy across programs.
- Work on extremely diverse and robust product pipeline
- Opportunity to work remotely for publicly traded organization
Responsible for long-range strategic planning and implementation for clinical and commercial manufacturing for the portfolio, development, and management of manufacturing, technical and engineering teams to drive the product-specific technology strategy, from development of clinical through commercial manufacturing.
- Build high performing team across Analytical Dev and Manufacturing
- Join a fast paced, growing Clinical Biopharmaceutical Company
The Head of Regulatory Affairs will oversee Regulatory Affairs and provide strategic input for CMC team activities for the development of submissions content and strategy for small molecule biologics products.
- Join a high growth, well-financed biotech organization focused on orphan drugs
- Opportunity to implement Regulatory CMC strategy for diverse program portfolio
Reporting to the CEO, this individual will play a key role in building and implementing a strategy for out-licensing of pre-clinical assets with Big Pharma partnerships. This individual will provide strategy on AI platform technologies as well as discovery collaboration with external companies. The VP of Strategy can be based anywhere on the East Coast.
- High-level role to build strategy for out-licensing efforts in Big Pharma.
- Global Machine Learning/AI biotech company which optimizes drug discovery.
The Director of Business Development, Bioanalysis will be responsible for generating sales for Bioanalysis throughout North America. This position will also contribute to the overall commercial sales strategies for sales of integrated preclinical and clinical development programs focused in North America.
- Join global CDMO leader with recently launched US Bioanalytical Services group
- Full time remote position with ownership over NA territory
Responsible for identifying, developing and executing business opportunities in the pharmaceutical, biotech industries on a global basis to strategically grow the business. Identify viable short and long term business opportunities in the CDMO space including CMC and GMP manufacturing and develop plans to convert opportunities into new business and revenue.
- Global CDMO in small molecule space seeking Sr. Director of Business Development
- Full time remote opportunity!
The VP of Regulatory Affairs will develop and execute the global regulatory strategy for our client's product pipeline and provide strategic leadership to oversee and direct all regulatory activities through early and late stage development.
- Exciting opportunity to build out Regulatory function at high-growth start up
- Own Regulatory aspects of programs approaching the clinic in both US and China
Responsible for efforts across pre-clinical and early development, including pre-clinical pharmacology, transnational science, toxicology and DMPK. Lead a senior, multi-disciplinary team to progress programs from discovery into early clinical development.
- Lead pre-clinical and early development activities
- Join an exciting pre-clinical company with a focus on immuno-oncology
The Director, Regulatory Affairs, CMC is responsible for the submission of INDs, NDAs, BLAs, as well as other regulatory submissions for CMC topics as required in collaboration with appropriate leadership.
- Join a growing biopharma company focused on Oncology
- Great opportunity to oversee a team changing the lives of cancer patients
The Director of Business Development, Bioanalysis will be responsible for generating sales for Bioanalysis throughout North America. This position will also contribute to the overall commercial sales strategies for sales of integrated preclinical and clinical development programs focused in North America.
- Join global CDMO leader with recently launched US Bioanalytical Services group
- Fully remote position with ownership over NA territory
The role requires significant experience and proven success with developing and executing regulatory strategies for complex drug development programs. The Senior Director serves as the regulatory lead for assigned product program teams and will manage other members of the regulatory affairs organization.
- Join a biotech company developing medicines for devastating diseases
- Exciting opportunity to serve as lead of Regulatory
The Director of Business Development, Bioanalysis will be responsible for generating sales for Bioanalysis throughout North America. This position will also contribute to the overall commercial sales strategies for sales of integrated preclinical and clinical development programs focused in North America.
- Join global CDMO leader with recently launched US Bioanalytical Services group
- Fully remote position with ownership over NA region
The Director of Business Development, Biologics will be responsible for both strategic and tactical selling of the Biologics production and manufacturing service portfolio utilizing highly consultative and technical sales strategies. Customers include biotech, pharma and large academic institutions.
- Global leader in drug R&D rapidly growing through expansion and investment
- Fully remote position with ownership over East Coast NA region
Serve as Quality function in this hands-on position overseeing, improving, and implementing the Quality Management System. Provide Quality related training. Coordinate internal and external quality audits. Internal subject matter specialist for regulatory strategy and implementation of filings and maintenance of approvals, trouble shooting, and regulatory authority interaction for product line.
- Leadership opportunity in terrific Medical Device Manufacturer
- Fully remote flexibility
The Quality Assurance Associate Director is responsible for directing a team of Quality professionals to develop and maintain a Quality culture on site.
- Exciting opportunity to build out Quality function at high growth facility
- Opportunity to partner with cutting edge Life Sciences Organizations
The Director of Business Development, Bioanalysis will be responsible for generating sales for Bioanalysis throughout North America. This position will also contribute to the overall commercial sales strategies for sales of integrated preclinical and clinical development programs focused in North America.
- Join global CDMO leader with recently launched US Bioanalytical Services group
- Fully remote position with ownership over NA territory
The Director of Business Development, Biologics will be responsible for both strategic and tactical selling of the Biologics production and manufacturing service portfolio utilizing highly consultative and technical sales strategies. Customers include biotech, pharma and large academic institutions.
- Global leader in drug R&D rapidly growing through expansion and investment
- Fully remote position with ownership full ownership of East Coast NA region
The Director of Business Development, Bioanalysis will be responsible for generating sales for Bioanalysis throughout North America. This position will also contribute to the overall commercial sales strategies for sales of integrated preclinical and clinical development programs focused in North America.
- Join global CDMO leader with recently launched US Bioanalytical Services group
- Fully remote position with ownership over NA territory
The Director of Business Development, Biologics will be responsible for both strategic and tactical selling of the Biologics production and manufacturing service portfolio utilizing highly consultative and technical sales strategies. Customers include biotech, pharma and large academic institutions.
- Global leader in drug R&D rapidly growing through expansion and investment
- Fully remote position with ownership over East Coast NA territory
The Associate Director, Regulatory Affairs will oversee regulatory activities for product programs and support and lead development of regulatory strategies. This role will execute program strategies and deliverables working in collaboration with relevant internal stakeholders.
- Opportunity to join a rapidly growing and publicly traded biotech organization
- Work on extremely diverse and robust product pipeline
You will form part of the HR leadership team, reporting to Global Head of HR. You will develop and execute the Americas people strategy to support business growth ambitions. You will define and implement a best-in-class strategy across all aspects of the employee life-cycle including; attraction and selection, diversity & inclusion, learning and development, engagement, performance management, compensation & benefits and retention.
- Global, market leading pharmaceutical organization
- Excellent opportunity to join a high performing business
The Director of Business Development, Bioanalysis will be responsible for generating sales for Bioanalysis throughout North America. This position will also contribute to the overall commercial sales strategies for sales of integrated preclinical and clinical development programs focused in North America.
- First Bioanalysis hire, ownership of the entire United States region.
- Join global CDMO leader; recently launched its US Bioanalytical Services group.
The Director of Business Development, Biologics will be responsible for both strategic and tactical selling of the Biologics production and manufacturing service portfolio utilizing highly consultative and technical sales strategies. Customers include biotech, pharma and large academic institutions.
- Head Biologics BD hire, looking to scale the business across the US region.
- Global leader in drug R&D rapidly growing through expansion and investment.
Our client is looking for a Global Strategic Workforce Planning Associate Director/ Director. This position is responsible for providing resourcing strategies on social media in order to get a fast and efficient resourcing.
- Very Remote Flexible Role!
- Client is world leader in using data, technology and advanced analytics!
Assist with the clinical development strategy, work with cross-functional multidisciplinary study teams on clinical trial strategy, design and execution. Serve as the Medical Lead and primary Medical Monitor for clinical trials that will be conducted with this compound.
- Assist in managing assets in company development portfolio
- Join a fast paced, growing Clinical Biopharmaceutical Company
This position will report to the VP of Clinical Operations and interact with the executive team. They will focus on building relationships with CROs and oversee the creation and implementation of standard operation procedures for clinical development.
- Opportunity to develop the Clinical Quality Function on the QA Team
- Join a clinical stage biotech company with wide pipelines
- Provide technical leadership in the design and development of next generation Cardiac 3D mapping and ablation SW platform and features.
- Build a global SW development team to develop and execute the overall Product Development plan
- A star project with focus on Electrophysiology Products (especially 3D Mapping)
- A strong international team with core know-how on 3D Mapping System
The Director - DMPK/ADME Lead will be responsible for overseeing ADME/DMPK strategies providing PK, in vitro/in vivo drug metabolism, drug disposition and PK/PD modeling and analysis for various projects. This role will establish oversee outsourcing, managing and reporting ADME/DMPK programs and studies.
- Join publicly traded clinical-stage biotech focused on neurological conditions
- Opportunity to implement and own ADME/DMPK function
This client is looking to hire a Director of Medicinal Chemistry or a Principal Scientist to lead and manage on-going and new Medicinal Chemistry Discovery projects. Much of the work is outsourced to CROs, which frees up the Director of Medicinal Chemistry to work remotely.
- Complex role to lead and manage on-going and new Discovery projects
- Full time remote position with ownership of the Medicinal Chemistry function
You'll be responsible with the BPMO for the successful implementation of a process-centric culture to improve quality & efficiency and to support delivery of changes and improvements to the business processes and procedures which underpin clinical trials. You'll also liaise and cooperate closely with BPMO in Process Quality and Learning (PQL).
- Dig deep into the biology of complex disease and uncover breakthroughs
- Push the boundaries of science and unleash your entrepreneurial spirit
