Sr. RA Associate Consultant

Remote; San Francisco (CA); Remote; USD 90,000 - 130,000; Full time

Job summary

ClinChoice is a global full-service CRO seeking a Sr. Regulatory Affairs Associate – CONSULTANT for a 12-month contract with potential extension to join one of our client teams.

This client-facing role requires independence, high-trust communication with the client's counterparts, and the ability to work with regulatory project teams to manage TDs and submissions per EU MDR and related global requirements. You will draft, review, and QC regulatory documents, coordinate with cross-functional

Qualifications

• Bachelor’s degree in life sciences
• Minimum of 2 years of experience in Regulatory Affairs focused on EU MDR
• Knowledge of EU MDR, ISO13485, and FDA Medical Device regulations
• Proficiency in Microsoft Office
• Strong communication and organizational skills

Responsibilities

• Collaborate with regulatory project team to review, update, and create Technical Documents (TDs) per EU MDR and other global requirements
• Identify applicable regulatory requirements, harmonized standards, guidance documents, and submission expectations
• Draft, create or update TDs in collaboration with Platform RA SME
• QC TD documents for completeness, pagination, and revision status
• Coordinate with cross-functional teams to obtain necessary supporting documents
• Respond to inquiries from local affiliates and coordinate with management on regulatory questions

Skills

Regulatory Affairs

EU MDR knowledge

FDA Medical Devices knowledge

Microsoft Office

Education

Bachelor’s degree in life sciences

Tools

Adobe PDF

Job description

Are you interested in working directly for a single sponsor while having the security and additional career opportunities that working for a global CRO can bring? Our team says it’s the best of both worlds….

ClinChoice is searching for a Sr. Regulatory Affairs Associate – CONSULTANT for 12 months Contract with possibility of extension to join one of our clients.

ClinChoice is a global full-service CRO with a strong focus on quality, professional development, and supportive culture. As a client-facing role, we are looking for confident candidates with the ability to work independently whilst establishing a high-trust environment with the client’s counterparts.

About the Role

Job Title: Sr. Regulatory Affairs Associate – CONSULTANT

Responsibilities:

• Regulatory Affairs Associate will actively collaborate with the Company’s regulatory project team to review, update, and create Technical Documents (TDs) in accordance with EU MDR and other applicable regulatory requirements. The high-level activities may include but are not limited to:

  • Establish and maintain an understanding of EU MDR and other global medical device regulatory requirements

  • Identify applicable regulatory requirements, harmonized standards, guidance documents, and submission expectations

  • Draft, create or update TDs in collaboration with Platform RA SME.

  • Review, obtain, and combine TF/DD documents in PLM or similar regulatory sources into Adobe PDF files

  • Create and upload bookmarks/indexes of the Adobe PDF files into PLM via Change Orders.

  • Perform Quality Control checks in accordance with client procedures, training, and checklists, including verification of completeness, correct pagination, and absence of blank or missing pages

  • Perform Quality Control checks per Company’s procedure/training/checklist, e.g., verify all pages are present, no blank pages, etc., Verify TD documents are approved and contain the most recent revision(s)

• Work with the cross functional teams and Company’s local affiliates to obtain necessary supporting documents

• Respond to inquiries from the Company’s local affiliates and proactively notify and coordinate with cross-functional teams including management any health authority–related questions or requests

• Represent Regulatory Affairs on project teams and report regulatory requirements in the frequency, format, and sequence as required

• Attend meetings and communicate with the project team as appropriate

• Routinely communicate with regulatory management team regarding project status and deliverables

• Support other regulatory activities as assigned

Minimum Requirements:

• Bachelor’s degree (life sciences preferred)

• Minimum of 2 years of working experience in Regulatory Affairs focused on EU MDR

• Knowledge of EU MDR, ISO13485, and FDA Medical Device regulations is mandatory

• Working proficiency in Microsoft Office (e.g., Word, Excel, PowerPoint)

• Self-starter with ability to work in team environment and projects of diverse scope where analysis of a situation or data requires evaluation of various factors with minimal supervision

• Strong organizational skills including attention to detail, good planning and communication skills are required

• Strong written and verbal English communication skills required.

Who will you be working for?

About ClinChoice

ClinChoice is a global full-service CRO specializing in clinical development and functional solutions for pharmaceutical, biotechnology, medical device, and consumer health companies. We have over 28 years of proven high-quality delivery and results across all our services, with over 4,000 professionals in more than 20 countries across the Americas, Europe, and Asia-Pacific.

Our Company Ethos

Our mission drives our culture: to contribute to a healthier and safer world by accelerating the development and commercialization of innovative drugs and devices. Our employees are the most valuable company asset and they are the fulcrum around which all ClinChoice activities are built and close management and training is the core instrument to develop and maintain highly-qualified personnel. The continuous training keeps the resources qualified in terms of competence and expertise and gives all personnel the clear tools needed to manage both internal and client processes with the same methodology. The success of these core values is evidenced by our below industry average turnover rates.

ClinChoice is an equal opportunity employer. We have based our success on attracting, developing, and promoting talent guided by diversity and inclusivity. Our employees come from very diverse backgrounds: gender, race, beliefs, and ethnicities. We recognize this is our strength and celebrate it.

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