Study Director
NAMSA, a Medical Research Organization, has created a unique strategy that starts with the end in mind. We take a medical device product all the way from concept to commercialization, with unmatched speed across the globe and with unparalleled capabilities through the entire product development process. By 2020 we plan to double the business as we did in the previous five years. Help us achieve our growth strategy and be a part of the company making an impact on improving and saving the lives of others
We are looking for a Study Director to join our Lab Services Division.
Responsibilities:
Serves as the Study Director for GLP studies and is the single point of control for straightforward multidisciplinary (In Vivo and In Vitro Biocompatibility, Chemistry, Microbiology) preclinical projects
Uncomplicated (routine) preclinical study design and protocol development
Establishes and ensures schedule, budget and quality commitments are met for the client
Manages (motivates, communicates) internal team members to ensure that client expectations are met
Understands investigational product(s) including high-level understanding of the Medical Device Development Process
Serves as the primary contact for the client, as assigned by management, and keeps the client informed of schedule and any unforeseen events or issues
Minimum
Qualifications:
Bachelor's degree in a scientific discipline with a minimum of 3 years of study director, laboratory or quality assurance experience
Project management experience preferred
AALAS certification recommended
We offer a competitive benefits package that includes:
Medical/Dental/Vision
Short/Long-Term Disability Coverage, Life Insurance
Health Savings and Flexible Spending Accounts
401k and Tuition Reimbursement opportunities
PTO and Paid Holidays
Wellness and Charitable Gift Matching Programs
. Apply now!Estimated Salary: $20 to $28 per hour based on qualifications.
We are looking for a Study Director to join our Lab Services Division.
Responsibilities:
Serves as the Study Director for GLP studies and is the single point of control for straightforward multidisciplinary (In Vivo and In Vitro Biocompatibility, Chemistry, Microbiology) preclinical projects
Uncomplicated (routine) preclinical study design and protocol development
Establishes and ensures schedule, budget and quality commitments are met for the client
Manages (motivates, communicates) internal team members to ensure that client expectations are met
Understands investigational product(s) including high-level understanding of the Medical Device Development Process
Serves as the primary contact for the client, as assigned by management, and keeps the client informed of schedule and any unforeseen events or issues
Minimum
Qualifications:
Bachelor's degree in a scientific discipline with a minimum of 3 years of study director, laboratory or quality assurance experience
Project management experience preferred
AALAS certification recommended
We offer a competitive benefits package that includes:
Medical/Dental/Vision
Short/Long-Term Disability Coverage, Life Insurance
Health Savings and Flexible Spending Accounts
401k and Tuition Reimbursement opportunities
PTO and Paid Holidays
Wellness and Charitable Gift Matching Programs
. Apply now!Estimated Salary: $20 to $28 per hour based on qualifications.
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