POSITION SUMMARY:
The Clinical Project Specialist is responsible for assisting with and/or completing projects related to the GC team and/or the clinical aspects of Natera products.
PRIMARY RESPONSIBILITIES:
- Assist in the development of patient consents, GC protocols, SOPs, GC note templates, patient education materials.
- Write or collaborate on abstracts or papers involving Natera tests.
- Deliver presentations/posters at scientific meetings and company promotional events as needed; represent company at trade shows and medical conferences (<10% travel).
- This role works with PHI on a regular basis both in paper and electronic form and has access to various technologies to access PHI (paper and electronic) in order to perform the job.
- Employee must complete training relating to HIPAA/PHI privacy, General Policies and Procedure Compliance training and security training as soon as possible but not later than the first 30 days of hire.
- Must maintain a current status on Natera training requirements.
- Perform other duties as assigned.
QUALIFICATIONS:
- Master’s degree (or equivalent) in Genetic Counseling or equivalent degree
- Board certified by the American Board of Genetic Counseling or the American Board of Medical Genetics
- Five or more years of clinical and/or laboratory GC experience
KNOWLEDGE, SKILLS, AND ABILITIES:
- In-depth technical understanding of Natera’s products
- Exceptional communication skills (oral and written) and attention to detail
- Demonstrated ability to work independently AND collaborate with team members
- Familiarity with Google and Microsoft suite of work products
- A desire to work for a dynamic and growing molecular genetics laboratory and manage growth for optimal success
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