What is a regulatory submission specialist?

As a regulatory submissions specialist, you create and maintain submission plans for regulatory operations processing. Your responsibilities are to develop departmental procedural documents, coordinate timelines for project plans, and to compile and prepare reports relating to cross-functionality of team members.

What is a submission specialist?

Job Description. Job Title: Regulatory Submission Specialist Job Summary: The Regulatory Submission Specialist is directly responsible for compiling, preparing, organizing, and filing regulatory related documents and reports of BioSpectra products, processes and systems.

What does a regulatory operations specialist do?

A regulatory affairs specialist is someone who works to help a company or organization meet all state, local, federal, international, and industrial regulations that apply to their products.

How much does a regulatory affairs specialist make in Canada?

Regulatory Affairs Specialist Salaries in Canada The national average salary for a Regulatory Affairs Specialist is $83,304 in Canada.

Is regulatory affairs a good career?

A career in Regulatory affairs is one of the versatile professions one can ever come across because it provides diversified employment opportunities that too at various levels. Even though Regulatory Affairs is one of the most interesting and rewarding careers but still it has its own challenges.

Is regulatory affairs job boring?

A career in regulatory affairs can be deceptively boring at the beginning. You need to push past this stage to get to the good stuff.

How do I become a regulatory specialist?

A detailed account of these basic steps follows.

  1. Step 1: Earn a bachelor’s degree (four years).
  2. Step 2: Get practical experience in the field (one to four years).
  3. Step 3: Complete advanced coursework in regulatory affairs (one to five years).
  4. Step 4: Obtain certification (several weeks or months).

What is a regulatory affairs Officer?

Regulatory affairs officers ensure the appropriate licensing, marketing and legal compliance of a range of pharmaceutical and medical products in order to control their safety and efficacy. As a regulatory affairs officer you’ll be the crucial link between your company, its products and regulatory authorities.

What is a regulatory affairs Associate?

The regulatory affairs associate is typically responsible for overseeing regulatory compliance and issues for their firm. This may include representing the regulatory branch of the company at meetings, overseeing technical documentation, and conveying the subject of that documentation to other staff.

Is regulatory affairs a boring job?

Is it hard to get into regulatory affairs?

Skilled regulatory affairs candidates are in high demand and vacancies for senior regulatory positions are easy to find, but many roles require experience and that can be hard to get.

How do I become a regulatory affairs specialist?

Most regulatory professionals have earned a bachelor’s degree, and more than half have an advanced degree, most often in a scientific or technical field. In addition, regulatory professionals usually have experience in other careers before transitioning into regulatory affairs.