Ashton Tweed is recruiting for several exciting life sciences opportunities. The following jobs represent a selection of our open positions. Qualified candidates for all positions are invited to submit their resumes to info@ashtontweed.com.

If you are a company interested in hiring for these or any roles throughout the entire life sciences discovery through commercialization continuum, please email us at partners@ashtontweed.com or call 610-725-0290 to speak with one of our life sciences partners.

Chief Medical Officer
Company: Clinical stage pharmaceutical company located in suburban Philadelphia that develops and commercializes novel therapeutics.
Description: The role provides strategic and tactical oversight to clinical development programs and to all Medical Affairs activities throughout the US.

Chief Financial Officer
Company: Clinical stage pharmaceutical company located in suburban Philadelphia that develops and commercializes novel therapeutics.
Description: The role provides oversight and counsel on both financial matters and financial leadership in the areas of business planning, financial budgeting and forecasting, and all accounting functions.

Vice President of Medical Affairs (Interim to Permanent role)
Company: Specialty pharmaceutical company based in the greater Cincinnati, OH region that develops and commercializes drugs.
Description: The role reports to the CMO and provides strategic and tactical oversight, medical input, advice and key opinion leader interaction, concerning: project planning for clinical trials and development programs, protocol development and review, and medical review of ongoing trials.

Vice President of Regulatory Affairs
Company: Pediatric pharmaceutical company headquartered in suburban Philadelphia.
Description: Reporting to the CEO, the VP of Regulatory Affairs is responsible for the development and implementation of a Regulatory Affairs strategy to ensure compliance with all applicable regulatory requirements throughout the drug development process to facilitate the successful and timely approval of regulatory applications. Requires at least 10 years broad-based experience in leading and managing US Regulatory Affairs.

Vice President of Manufacturing
Company: Pediatric pharmaceutical company headquartered in suburban Philadelphia.
Description: Reporting to the CEO, the VP of Manufacturing is responsible for managing the supply chain team to ensure the uninterrupted supply of high quality products to patients for the purpose of current clinical trials at a reasonable cost.  The role will work with the CMO to develop scale up methods and processes in preparation for the commercial launch of the company’s new pharmaceutical preparation.

Marketing Director
Company: Australia-based pharmaceutical company entering the United States market with offices located in the suburban Philadelphia region.
Description: Reporting to the U.S. President the Marketing Director will facilitate the planning, developing, and executing of strategic plans for the U.S. market, including brand strategy, promotions, opinion leader development, positioning and messaging, new markets development, and sales and marketing integration in support of the U.S. business strategies.

Director, Regulatory Affairs and Operations
Company: Biopharmaceutical company located in central New Jersey.
Description: Reporting to the Executive Vice President, the Director, Regulatory Affairs and Operations is responsible for planning and coordinating regulatory submissions necessary to support clinical trials and product registration. The role will represent the company with domestic and international regulatory authorities and provide regulatory support for various departments, projects, and teams/committees.

Director, Business Development
Company: Global drug delivery company headquartered in suburban Philadelphia.
Description: The role identifies customers for co-development collaborations that utilize proprietary technologies, manages the team that works within the US group on outreach activities, and negotiates and closes technology and product out-licensing transactions.

Director of Medical Affairs
Company: Global Specialty pharmaceutical company headquartered in suburban Philadelphia.
Description: Responsible for supporting the sales and marketing organizations with development and review of medical education programs and materials. The role assists with salesforce training and support of all in-licensing opportunities.

Senior Clinical Quality Assurance Specialist
Company: Biopharmaceutical company in suburban Philadelphia.
Description: Responsible for conducting series of GCP audits of Phase I- III clinical research trials to assure compliance with all government regulations.

Project Manager (Interim to Permanent role)
Company: Pediatric pharmaceutical company headquartered in suburban Philadelphia.
Description: This role assists the CEO in managing and controlling all aspects of the company’s product development projects from development to commercialization. Requires excellent understanding of pharmaceutical manufacturing process, extensive experience in FDA regulations and in working with contract manufacturers and contract research organizations.

Clinical Project Manager
Company: Clinical stage pharmaceutical company located in suburban Philadelphia that develops and commercializes novel therapeutics.
Description: This role manages all phases of national and international clinical trials to ensure patient safety and data integrity, develops study documents and has active involvement in developing and refining Clinical Department processes.

Clinical Project Manager (Greater Philadelphia Region)
Company: The company, located in the greater Philadelphia region, develops and markets therapeutic drugs.
Description: This role manages all phases of national and international clinical trials to ensure patient safety and data integrity, develops study documents and has active involvement in developing and refining Clinical Department processes.

Clinical Operations Manager 
Company: Specialty pharmaceutical company headquartered in the UK with offices in the greater Philadelphia region.
Description: The role is responsible for the execution of the clinical development program from protocol design to the final clinical study report. Will also provide the overall cross-functional leadership to achieve project objectives on time and within the budget.

If your skills match the positions above or you would like additional information on our open positions, we invite you to send your resume to info@ashtontweed.com. Please forward this message to any interested colleagues.

Ashton Tweed
620 Lee Road, Suite 130
Wayne, PA 19087
Phone: 610-725-0290
info@ashtontweed.com