Regulatory Affairs Associate

Who Are We?

Founded in 1997 and built upon 26+ years of dermatology-specific experience, we are the only full-service dermatology CRO that takes products from concept to approval. Voted one of San Diego’s Top Workplaces, we take pride in maintaining a company culture that values collaboration, diversity of background and thought, and dedicated talent. When you join Therapeutics, you are not a number or a cog in the wheel, you are valued for your unique and important contributions that you bring to our team and our clients.

Who Are You?

You are a dedicated individual who is passionate about your work and you want to join a team that believes a company is only as successful as its people. You lead with humility and know that your individual contribution is important to the team so you take pride in delivering great work. You believe anything worth doing, is worth doing right. You communicate clearly and have great attention to detail. You love to collaborate with the team but are able to think on your feet to problem-solve independently.

What is the Primary Objective of the Regulatory Affairs Associate?

Your Main Responsibilities and Duties Include:

• Plan, compile, publish and submit Regulatory documents for IND, NDA, BLA, IDE, and PMA applications, including Amendments, Supplements, and Meeting materials to the FDA.
• Review submission components for quality and completeness.
• Assure all electronic submissions are in compliance with regulatory requirements and ICH eCTD specifications.
• Maintain Regulatory submission and correspondence archive/records.
• Provide publishing support to the Medical Writing group, as requested.
• Provide regulatory support to other departments, as requested.
• Assist Regulatory Director in providing regulatory strategy, intelligence, and other regulatory support to product development teams.
• Serve as a point of contact for the FDA.    

To Succeed in this Position:

• You should have a scientific background (BS degree or equivalent knowledge and experience).
• At least two (2) years of experience in Regulatory Operations/electronic submissions.
• You should have technical knowledge in eCTD compliant submissions and experience with off-the-shelf publishing software.
• Good understanding of FDA’s submission requirements and drug/biologic/device development processes is required.
• You must have excellent written and oral communication skills, with the ability to manage multiple priorities.

The most likely starting base pay range for this position is $65,000 to $70,000 per year. Several factors, such as experience, tenure, skills, geographic location and business needs will determine an individual’s exact level of compensation. Consideration will be given to experience that exceeds the listed requirements.

We at Therapeutics, Inc. are committed to providing an environment of mutual respect where equal employment opportunities are available to all applicants and team members without regard to race, color, religion, marital status, age, national origin, ancestry, physical or mental disability, medical condition, pregnancy, genetic information, gender, sexual orientation, gender identity or expression, veteran status, or any other status protected under federal, state, or local law. If you are smart and good at what you do, we welcome you to apply!