What are the responsibilities and job description for the FDA Associate Attorney position at Illapa Search?
About:
A very prestigious and successful global law firm is seeking an associate to join their Healthcare, Life Sciences, FDA & Regulatory Practice Group in Missouri. Their healthcare and life sciences practice group includes former professionals from FDA and DOJ, whom have been honoured by Chambers USA, Legal 500, and LMG Life Sciences.
With over 17 offices and 1,500 attorneys across the globe, this leading international law firm works with vital and renowned industries and clients, from regulatory matters to high-stakes litigation. They have been awarded and honoured by The American Lawyer, The Legal 500, The Best Lawyers in America, and Fortune, for titles such as ‘Best Company to Work For’ and ‘Best Workplace for Women’.
Experience:
- Candidates will have 2 years of regulatory experience advising life sciences and health care clients on a variety of healthcare regulatory issues, especially on FDA regulations and compliance.
- Relevant experience in aspects of health regulatory law applicable to the development and commercialization of FDA-regulate products, such as fraud and abuse, advertising and promotion, and/or clinical research, is beneficial.
- Experience negotiating commercial agreements is preferred, but not essential.
- Applicants must possess strong academic credentials, and excellent communication, interpersonal, and analytical skills.
- A technical background or Master’s in Public Health (or another related subject) is preferred, but not required.
Responsibilities:
- Analyzing, counseling and structuring arrangements between and among referral sources for compliance with fraud and abuse laws, including False Claims Acts, state and federal anti-kickback laws, and unprofessional conduct regulations.
- Advising and implementing compliance program infrastructures, like policies and procedures, to board of directors and compliance personnel.
- Advising on all aspects of advertising of drug and medical devices, marketing and promotional compliance, for example labelling and advertising claims review, social media and interactions with HCPs.
- Draft and negotiate a wide variety of agreements between manufacturers , healthcare and life science providers etc.
- Conducting regulatory due diligence reviews to identify and assess risks.
Benefits:
- Outstanding benefits package, including a wider range of health support and coverage, family leave, and alternative work schedules for familial aid.
- Leverage concierge, errand running, and Medicare.
- Fantastic opportunity for career growth and progression.
How to Apply:
Thank you for interest in this role. Please click on the ‘apply now’ and attach your resume to be considered for this position.
Job Type: Full-time
Schedule:
- Monday to Friday
Work Location: One location
Salary : $131,000 - $166,000
