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Internship Regulatory Science Jobs (NOW HIRING)

Everman ISD

Science Teacher

Fort Worth, TX

$46K - $59K/yr

At least one year student teaching or approved internship Major Responsibilities and Duties ... regulations. 4.Plan and use appropriate instructional and learning strategies, activities ...

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How much do internship regulatory science jobs pay per month?

As of Jul 23, 2026, the average monthly pay for internship regulatory science in the United States is $6,439.50, according to ZipRecruiter salary data. Most workers in this role earn between $4,416.67 and $7,666.67 per month, depending on experience, location, and employer.

Which is better, RA or QA?

For an Internship in Regulatory Science, QA (Quality Assurance) focuses on ensuring compliance with standards and procedures, while RA (Regulatory Affairs) involves preparing and submitting documentation to regulatory agencies. Both roles are important; QA emphasizes process validation and audits, whereas RA emphasizes regulatory strategy and documentation. The choice depends on whether you prefer quality control or regulatory compliance tasks.

What are the big 4 internships?

The 'Big 4' internships typically refer to internship programs offered by the four largest professional services firms: Deloitte, PricewaterhouseCoopers (PwC), Ernst & Young (EY), and KPMG. These firms offer internships in areas such as regulatory science, accounting, consulting, and audit, providing valuable experience and potential pathways to full-time roles in the industry.

What can you do with a regulatory science degree?

A regulatory science degree prepares individuals for roles in regulatory affairs, compliance, and quality assurance within the pharmaceutical, biotech, and healthcare industries. Graduates can work as regulatory specialists, compliance officers, or in drug development, often utilizing knowledge of regulations, policies, and tools like submission documentation and clinical trial processes.

What does a regulatory intern do?

A regulatory intern assists with preparing and reviewing documentation to ensure compliance with industry regulations and standards. They may support regulatory submissions, conduct research on regulatory requirements, and help maintain regulatory databases, often using tools like Microsoft Office and regulatory information systems. The role provides exposure to the regulatory approval process and industry-specific compliance practices.

What is the difference between Internship Regulatory Science vs Regulatory Affairs Associate?

AspectInternship Regulatory ScienceRegulatory Affairs Associate
CredentialsTypically students or recent graduates, some certifications optionalBachelor's degree, certifications like RAC beneficial
Work EnvironmentInternship setting, learning-focused, temporaryFull-time professional role, ongoing responsibilities
Industry UsageEntry-level, educational programs, trainingEstablished industry role, compliance and submission tasks

Internship Regulatory Science is an entry-level, learning-focused position for students or recent graduates, often temporary. Regulatory Affairs Associates are full-time professionals responsible for compliance and submissions, requiring more experience and credentials. Both roles are essential in the regulatory industry but differ mainly in experience level and responsibilities.

What cities are hiring for Internship Regulatory Science jobs? Cities with the most Internship Regulatory Science job openings:
What are the most commonly searched types of Regulatory Science jobs? The most popular types of Regulatory Science jobs are:
What states have the most Internship Regulatory Science jobs? States with the most job openings for Internship Regulatory Science jobs include:
Internship Regulatory Science jobs near you
Director, Regulatory Affairs

Director, Regulatory Affairs

Cytokinetics

South San Francisco, CA • On-site

$225K - $262K/yr

Full-time

This job post has expired today. Applications are no longer accepted.

Job description

Cytokinetics is a specialty cardiovascular biopharmaceutical company, building on its over 25 years of pioneering scientific innovations in muscle biology, and advancing a pipeline of potential new medicines for patients suffering from diseases of cardiac muscle dysfunction.
Reporting to the Senior Director, Regulatory Affairs, the Director, Regulatory Affairs is responsible for leading regulatory support for assigned programs to ensure sound regulatory planning and tactical implementation of US and international development strategies.
Responsibilities:
  • Formulates regulatory strategies, with supervisor oversight, to support program objectives and oversees implementation of regulatory strategy and activities needed to secure approval of new drugs
  • Serves as a regulatory affairs lead on assigned clinical studies to support the development and execution of global regulatory strategies and provide regulatory advice to other functions
  • Identifies gaps in product development plans that may pose regulatory risks and identifies related solutions and mitigation plans
  • Builds and maintains collaborative relationships with cross-functional project teams, other departments, vendors, and external business partners to achieve program regulatory goals
  • Manages coordination, preparation, and timely submission of regulatory documents, filings, and responses to queries
  • Reviews global regulatory submissions for consistency and quality across regions
  • Maintains current knowledge of laws, regulations and guidelines (eg, FDA, EMA, ICH, CDE, PMDA), as needed to support global programs
  • Ensures conformance to commitments made with various regulatory agencies (eg, IND/CTA commitments, annual obligations) for assigned programs
  • Contributes to regulatory department initiatives, including the development and maintenance of internal regulatory processes, operating guidelines, templates, and best practices
  • Supervises employees, consultants/contractors, and/or interns in Regulatory Affairs
  • Mentors department personnel and optimizes employee performance by developing employees and promoting career growth

Qualifications:
  • 10+ years of drug development, including at least 7+ years of regulatory affairs experience in the Biotech/Pharmaceutical industry; experience in small molecule drug development is preferred; experience in the cardiovascular therapeutic area is a plus
  • Bachelor's degree is required, preferably in a scientific discipline; advanced degree (MD, PharmD, or PhD) is a plus
  • Excellent working knowledge of international regulatory requirements and environment applicable to the clinical development and post-marketing space, including an understanding of GXP
  • Demonstrated knowledge of the regulatory requirements in the design and conduct of clinical trials, including the preparation of regulatory submissions
  • Experience with eCTD requirements and electronic submissions
  • Experience with international regulatory submissions and processes (eg, Canada, greater China, Japan) is a strong plus
  • Demonstrated management expertise, including leadership and development of employees
  • Ability to work effectively across teams, functions and with external partners
  • Excellent oral and written communication skills
  • Excellent organizational and time management skills, attention to detail, and ability to independently drive deliverables to completion
  • Ability to work effectively in a fast-paced environment while managing multiple priorities
    #LI-HYBRID

Pay Range:
In the U.S., the hiring pay range for fully qualified candidates is $225,000 - $262,500 per year. The base pay actually offered will take into account internal equity and also may vary depending on the candidate's geographic region, job-related knowledge, skills, and experience among other factors.
Our employees come from different backgrounds, and we celebrate those differences. We are looking for the best candidates for our open roles, but do not expect applicants to meet every qualification in order to be considered. If you are excited about what you could accomplish at Cytokinetics and believe you can add value to our team, we would love to hear from you.
Please review our General Data Protection Regulation (GDPR) policy PRIOR to applying.
Our passion is anchored in robust scientific thinking, grounded in integrity and critical thinking. We keep the patient front and center in all we do - all actions and decisions are in service of the patient and their caregivers. We champion integrity, ethics, doing the right thing, and being our best selves.
Fraud Warning: How to Identify Impersonated Cytokinetics Job Postings and Offers
Recently, there have been fraudulent employment offers being sent to candidates on behalf of Cytokinetics. Please be advised that all legitimate offers from Cytokinetics will come directly from our official email domain (Cytokinetics.com) and will only be made after completing a formal interview process.
Here are some ways to check for authenticity:
  • We do not conduct job interviews through non-standard text messaging applications
  • We will never request personal information such as banking details until after an official offer has been accepted and verified
  • We will never request that you purchase equipment or other items when interviewing or hiring
  • If you are unsure about the authenticity of an offer, or if you receive any suspicious communication, please contact us directly at talentacquisition@cytokinetics.com

Please visit our website at: www.cytokinetics.com
Cytokinetics is an Equal Opportunity Employer

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