Sterling-Hoffman Executive Search
Home
Our Story
Domain Expertise
Clients
Career Opportunities
Community
Contact Us
Submit your resume
Interviewing Guidelines








    
Sign-up
for the Sterling-Hoffman Life Sciences Journal to get the latest industry news and job postings.
Sterling Life Sciences, Specialists in Pharmaceuticals, Healthcare and BioTech Recruitment
Career Opportunities

Back

To apply for multiple jobs at once, please select the check box beside the desired jobs on the main job category page.

 Job #03018 Email this job to a friend
About our client
Our client is a leading medical device company. They have a leadership position in their targeted markets and an established reputation as a leading innovator in the field. The company has premier investors and a strong pipeline. This is a great opportunity for the right candidate.
Position Location
Clinical Affairs Manager New Jersey
Salary
Highly competitive package, commensurate with experience
Responsibilities
1) Handle pre-market and post-market submissions including preparation of IDEs and corresponding PMAs
2) Ensure company compliance with FDA regulatory requirements for clinical studies
3) Manage clinical trials and supervise regulatory specialists
4) Create and submit pre-market submissions (IDEs, PMAs and related supplements/amendments)
5) Develop and implement procedures for the Clinical Department
6) Manage implementation of studies and ongoing study activities
7) Ensure proper monitoring of studies
8) Train employees on internal procedures
9) Ensure maintenance of data and record keeping
10) Support the company during inspections/audits by the FDA, notified bodies or other international regulatory bodies
11) Supervise employees directly and carry out supervisory tasks as per organization's policies and applicable laws
12) Interview, hire and train employees in India office
13) Plan, assign and direct work
14) Appraise performance as well as reward and discipline employees (as needed)
15) Address complaints and resolve problems
Requirements
1) Bachelor’s degree in Engineering, Biological/Life Sciences or Nursing (Master’s degree preferred)
2) 2 years of clinical/regulatory experience
3) Knowledge of medical devices or biologics and statistics preferred
4) In-depth knowledge of FDA and regulations (interpretation and monitoring)
5) Ability to understand and define problems, collect data, establish facts and draw valid conclusions
6) Ability to read, analyze and interpret common scientific and technical journals, financial reports as well as legal documents
7) Ability to respond to common inquiries or complaints from customers, regulatory agencies or members of the business community
8) Ability to effectively present information to top management and team members
9) Ability to apply mathematical operations to such tasks as frequency distribution, analysis of variance, correlation techniques and factor analysis
10) Excellent computer skills (MS Excel and Word)
11) Willingness to travel internationally (up to 30%)

Back
Home | Our Story | Domain Expertise | Clients | Career Opportunities | Community | Contact Us