Senior Clinical Engineering Manager at Jobot San Jose, CA 95134
This Jobot Job is hosted by:
Emily OlingerAre you a fit? Easy Apply now by clicking the Apply at employer's site button and sending us your resume.
Salary:
$140,000 - $200,000 per yearA bit about us:
We are an industry leader in computer vision and healthcare with an award winning flagship product.
Our team's goal is to digitally augment clinicians with software to improve diagnostic accuracy and improve patient safety
clinical outcomes.
We are looking for a Clinical Engineering Manager with experience in writing lab protocols and working in a wet lab with GLP/GCP, if this sounds like you, please keep reading and apply today! Location:
San Francisco Bay area (we are a VIRTUAL company! Occasional travel to operation center is required, travel to labs/clinical trials, operating rooms, and field work is required.
Level:
Senior ManagerWhy join us?Start up culture with great stock options100% EMPLOYER PAID Blue Shield PPO insurance
Disability insurance 401k 5 weeks of PTO, 2 flex days, and all major holidaysGREAT BONUS STRUCTUREJob DetailsThe Senior Manager of Clinical Engineering is a work from home role with field travel to our clinical trial locations and operating rooms (across the US) and to our operation center to pick up equipment (Menlo Park, CA).
You must be comfortable with being in the field with possible exposure to SARS-CoV-2 (will full PPE).
You will be working on a small team consisting of 2 Clinical experts and occasional temporary employees
vendors running trials.
Leadership experiene is required.
Extensive experience writing Lab Protocols and Clinical Trial Reports for the FDA.
Extensive experience working in a Wet Lab setting (we work with blood, viruses, human tissue, etc.
) following GLP/GCP.
Experience running a Clinical Trial with 3rd parties.
Must be hands on and work in the lab as needed.
Experience with the CAPA process (Corrective Action Preventative Action) and responses to the FDA.
Experience filing 510(k) FDA applications.
ISO 13485 (framework we use for developing medical products).
Bonus Points:
Background in Data Analytics or managing data in a lab settingPythonPh.
D.
or advanced degreeStart up experienceInterested in hearing more? Easy Apply now by clicking the Apply at employer's site button.
.
Estimated Salary: $20 to $28 per hour based on qualifications.
Emily OlingerAre you a fit? Easy Apply now by clicking the Apply at employer's site button and sending us your resume.
Salary:
$140,000 - $200,000 per yearA bit about us:
We are an industry leader in computer vision and healthcare with an award winning flagship product.
Our team's goal is to digitally augment clinicians with software to improve diagnostic accuracy and improve patient safety
clinical outcomes.
We are looking for a Clinical Engineering Manager with experience in writing lab protocols and working in a wet lab with GLP/GCP, if this sounds like you, please keep reading and apply today! Location:
San Francisco Bay area (we are a VIRTUAL company! Occasional travel to operation center is required, travel to labs/clinical trials, operating rooms, and field work is required.
Level:
Senior ManagerWhy join us?Start up culture with great stock options100% EMPLOYER PAID Blue Shield PPO insurance
Disability insurance 401k 5 weeks of PTO, 2 flex days, and all major holidaysGREAT BONUS STRUCTUREJob DetailsThe Senior Manager of Clinical Engineering is a work from home role with field travel to our clinical trial locations and operating rooms (across the US) and to our operation center to pick up equipment (Menlo Park, CA).
You must be comfortable with being in the field with possible exposure to SARS-CoV-2 (will full PPE).
You will be working on a small team consisting of 2 Clinical experts and occasional temporary employees
vendors running trials.
Leadership experiene is required.
Extensive experience writing Lab Protocols and Clinical Trial Reports for the FDA.
Extensive experience working in a Wet Lab setting (we work with blood, viruses, human tissue, etc.
) following GLP/GCP.
Experience running a Clinical Trial with 3rd parties.
Must be hands on and work in the lab as needed.
Experience with the CAPA process (Corrective Action Preventative Action) and responses to the FDA.
Experience filing 510(k) FDA applications.
ISO 13485 (framework we use for developing medical products).
Bonus Points:
Background in Data Analytics or managing data in a lab settingPythonPh.
D.
or advanced degreeStart up experienceInterested in hearing more? Easy Apply now by clicking the Apply at employer's site button.
.
Estimated Salary: $20 to $28 per hour based on qualifications.
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