Manager, Translational Research Juventas Therapeutics
THIS JOB HAS EXPIRED
DEPARTMENT: Product Development
POSITION REPORTS TO: Vice President, Product Development
JOB TYPE: Full Time
GENERAL SUMMARY:
Juventas Therapeutics is a venture-backed, clinical-stage biotechnology company developing novel therapies for
treatment of a cardiovascular disease. The Manager, Translational Research will be responsible for overseeing all aspects of
developing novel therapeutic strategies through pre-clinical studies into human clinical trials. Preferred candidates will have
significant cardiovascular research experience preferably within the heart failure and/or regenerative medicine fields. The position
will require a strong technical background with demonstrated capabilities in designing and managing animal studies and
transitioning technologies from pre-clinical to clinical stages through submission of Investigational New Drug (IND) applications.
Adaptability and comfort working in a fast-moving, highly-dynamic start-up environment are a must.
Highly developed interpersonal written and oral communication skills, attention to detail, effective computer skills and
project management skills are required. The successful candidate will be highly organized and capable of working within a team to
assure assignments are completed on time. Key responsibilities will include managing all aspects of pre-clinical study design and
execution including IND preparation and submissions. In addition, candidates must have flexibility to take on new tasks as they
arise within the company. We are looking for self-motivated individuals interested in science and drug development as part of their
career development.
MINIMUM QUALIFICATIONS:
Education, Knowledge, Skills and Abilities
The successful candidate at a minimum should have a doctoral degree, preferably in cardiovascular research and/or
regenerative medicine. A master?s degree in engineering or life sciences with significant work experience may also be
appropriate. The proper candidate will have strong therapeutic product development experience preferably in the area of
transitioning technologies into early stage clinical trials. Strong technical writing skills are a must and experience working with
the FDA on therapeutic product approvals is preferred. The proper candidate will be a self-starter and willing to work in a
dynamic, high-paced start-up environment.
Required Length and Type of Experience
The successful candidate will have minimum of 3 years experience working at a biotechnology or pharmaceutical company
having developed products for clinical trials. Experience in gene therapy, biologics and/or cardiovascular product development a
plus. Must have experience in organizing, summarizing, and communicating scientific results through publication or engagement
with the FDA. Experience with negotiating or managing contracts with contract vendors is a plus.
PRINCIPLE DUTIES AND RESPONSIBILITIES:
1. Designing and managing all aspects of pre-clinical animal studies
2. Overseeing vendor and contractor relationships related to development of new products
3. Involvement in developing regulatory strategy to introduce new therapies to the clinic
4. Writing Investigational New Drug (IND) applications
5. Sourcing grant funding to develop emerging therapeutic opportunities
6. Other tasks as assigned
| Location: |
Cleveland, OH
United States
|
THIS JOB HAS EXPIRED