Biotech Jobs

 Responsibilities 

• Partners with sales representatives during the sales process, providing technical expertise and application support
• Works internally with New Product Development engineers to assist in planning and executing evaluation projects for technology development, application development, and process development associated with single-use systems.
• Provides information relating to market trends, business conditions, and competitive activities to management team and Research and Development (R&D)
• Acts as the customer interface and liaison to address scientific and technical issues with the Product Development Team.
• Provides training on products, systems, and methods to customers and internal staff.
• Assists Product Development Engineers in the characterization and evaluation of Charter products prior to commercialization.
• Together with the sales team, develops and maintains strong business relationships with current and prospective customers
• Works within the sales funnel utilizing CRM, prioritizing qualified targets, writing post-call reports, and updating customer contact information
• Follows up on samples and customer projects related to the sales process.
• Maintains technical competency in the cell therapy and bioprocessing industry, including product technologies, application techniques, and regulatory issues which impact customers.
• Performs all other job-related duties as assigned.

Requirements

 B.S. in Biochemistry, Biochemical Engineering, or equivalent discipline. Minimum 2 years’ experience in biotechnology/cell therapy process development. Experience in a CRO or CDMO is preferred. Excellent communication and organizational skills.

 Responsibilities

• Assists principal investigator and other health professionals in troubleshooting various problems related to the management of the clinical study. Assists in all aspects of the data collection process.
• Responsible for recruitment of patients for the clinical study including tracking the sources of patient referrals. Responsible for coordinating, scheduling, and supervising the study visit.
• Responsible for obtaining consent, medical history, and other data collection forms.
• Maintains appropriate patient records as necessary. This includes charting the condition of the patient and determining their continued eligibility in the study. Enters data from the participant’s data collection forms into the study website and resolve queries generated by the statistician.
• Obtains and interprets pertinent data from medical records as needed to understand past and present condition of the patients.
• Performs technical procedures on clinical subjects under the direction of the principal investigator or his/her designee.
• Administers cognitive/memory tests to the study participants.
• Notifies the participant and their physician (per participant request) of study results and/or alerts that may require follow-up.
• Performs day-to-day administrative and clerical duties such as designing brochures, stationary and data forms. Creates reports and graphs pertinent to the study including presentation of the results of the study.
• May supervise other personnel including volunteers as assigned.
• Assists in development of suitable codes and data collection forms for computerization.
• Consults and cooperates with all faculty, coordination centers, sponsors, and health professionals involved in the clinical study.
• Performs other related duties incidental to the work described herein.

Requirements

Bachelor’s degree in a related field of study or an equivalent combination of experience and education. Experience in a medical and/or research setting.