Career Opportunity Listings
Ashton Tweed is currently recruiting for a number of excellent opportunities in the life sciences. The following is a representative selection of our open positions. If you are a qualified candidate who is interested in applying for any of these listings, please submit your resume to info@ashtontweed.com and include the job title in the subject line of your email.
- Associate Director, Medical Writing
Description: Provides technical and editorial expertise and administrative guidance to medical writers within the Worldwide Clinical Research Department with regard to regulatory document preparation processes, standards, quality, and timeliness in support of drug development, product registrations, and product marketing. The incumbent creates, revises, and maintains document templates; manages and oversees document quality control; coordinates clinical quality assurance workflow; and edits and critically reviews regulatory documents. Depending on the structure of the group, the role may be mainly focused on the operational aspects of document preparation or on document review, editing, and writing.
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- Director, Clinical Affairs (Medical Device)
Description: The Director, Clinical Affairs is responsible for the management of all clinical affairs for the company’s products, as well as supporting marketing and other product management activities. The Director, Clinical Affairs works closely with other internal departments and external parties (such as distributors and industry collaborators) to meet the clinical, marketing, and product management goals for the company’s products.
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- U.S. Sales Director
Description: A biotech company that is a leader in genome customization is searching for a U.S. Sales Director to work directly with academic and industry customers, assess marketplace needs, identify leads, as well as promote and close sales. The company brings easy and ready-to-use research tools to the life sciences community to generate cells with desired characteristics and performance.
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- Interim Clinical Project Analyst
Description: This position is responsible for the clinical trial cost projections, as well as tracking versus those projections. If the capabilities align, additional general accounting activities will be required.
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- Tax Manager
Description: The qualified candidate will have 3 to 5 years of corporate tax management experience for federal and state taxes, a BS in accounting or related discipline, and the ability to speak Japanese fluently. A CPA is preferred. The qualified candidate will also demonstrate PC proficiency in MS Excel, Word, and PowerPoint, expert knowledge level of financial reporting of income taxes and tax-return preparation and filing, as well as a full understanding of GAAP. In addition, the Tax Manager must have the ability to communicate with senior management, the audit firm, and the Japanese parent company.
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- Manager/Senior Manager Medical Information
Description: The primary responsibility is to manage medical information and communication for assigned products marketed by our client by providing prompt, accurate, and scientifically and medically balanced responses to unsolicited medically related inquires from internal and external customers. The responsible individual will work closely with key members of internal departments, including legal, regulatory affairs, sales, and marketing, to provide medical support for development, implementation, maintenance, and enhancement of ongoing medically related activities associated with the client’s marketed product(s). All Standard Operating Procedures and related documents should be followed accordingly.
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- Director Biometrics
Description: Provides technical leadership and biostatistical support on the design and conduct of clinical studies. The Director Biometrics participates in the evaluation, interpretation, and reporting of study results and regulatory submissions to the FDA and other regulatory agencies. The successful candidate will perform statistical analyses and develop tracking systems for data quality assurance. This position will also manage biostatisticians and/or SAS programmers.
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- Life Sciences Patent Attorney (Boston-based firm)
Description: The qualified candidate will have worked more than 8 years in a patent law firm and have experience in biotechnology/life sciences. A PhD is critical, although a prolific person with many years of experience and significant book of business will be considered. The candidate must have a passion for building a patent law practice in the life sciences.
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- Project Manager
Description: Our client is looking for a Project Manager to act as a central point of contact for information and project flow across the organization. The company is a contract manufacturing organization providing development and manufacturing services to pharmaceutical, diagnostic, and biotech companies. The company supports the development and commercialization of drug, biopharmaceutical, and diagnostic products of its clients.
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