Senior Associate - Regulatory Affairs What you will do Let's do this. Let's change the world. In ... Strong communication skills - both oral and written * Ability to understand and communicate ...
Senior Associate - Regulatory Affairs What you will do Let's do this. Let's change the world. In ... Strong communication skills - both oral and written * Ability to understand and communicate ...
Associate or Senior Associate, Regulatory Affairs
Denver, CO · On-site
$93K - $113K/yr
Position Overview The Associate or Senior Associate, Regulatory Affairs will report to the Director ... Develop and deliver written and/or oral internal presentations on relevant regulatory updates ...
Associate or Senior Associate, Regulatory Affairs
Denver, CO · On-site
$93K - $113K/yr
Position Overview The Associate or Senior Associate, Regulatory Affairs will report to the Director ... Develop and deliver written and/or oral internal presentations on relevant regulatory updates ...
Senior Associate, Regulatory Affairs
Lake Forest, IL · On-site
$97K - $139K/yr
Present scientific data effectively orally and in writing in logical and persuasive manner. * Provides daily regulatory support to new product development teams and commercial support with guidance.
Senior Associate, Regulatory Affairs
Lake Forest, IL · On-site
$97K - $139K/yr
Present scientific data effectively orally and in writing in logical and persuasive manner. * Provides daily regulatory support to new product development teams and commercial support with guidance.
Senior Associate, Regulatory Operations
Berkeley Heights, NJ · Remote
$115K - $135K/yr
Publishes US Regulatory Submissions to the Food and Drug Administration: NDAs, INDs, ANDAs ... Strong written and verbal communication skills. * Computer skills required: Microsoft Word, Adobe ...
Quick apply
Senior Associate, Regulatory Operations
Berkeley Heights, NJ · Remote
$115K - $135K/yr
Publishes US Regulatory Submissions to the Food and Drug Administration: NDAs, INDs, ANDAs ... Strong written and verbal communication skills. * Computer skills required: Microsoft Word, Adobe ...
$93K - $113K/yr
Position Overview The Associate or Senior Associate, Regulatory Affairs will report to the Director ... Develop and deliver written and/or oral internal presentations on relevant regulatory updates ...
$93K - $113K/yr
Position Overview The Associate or Senior Associate, Regulatory Affairs will report to the Director ... Develop and deliver written and/or oral internal presentations on relevant regulatory updates ...
Senior Associate, Regulatory Operations
$25.94 - $34.43/hr
Overview The Senior Associate, Regulatory Operations is a project-level lead who is responsible for ... Clear, concise technical writing ability Preferred * Experience working on cross-functional teams
Senior Associate, Regulatory Operations
$25.94 - $34.43/hr
Overview The Senior Associate, Regulatory Operations is a project-level lead who is responsible for ... Clear, concise technical writing ability Preferred * Experience working on cross-functional teams
Trading Desk Associate Regulatory Analyst
Manhattan, NY · On-site
$125K/yr
Trading Desk Associate Regulatory Analyst (BH-400063) Location New York, United States Sector ... Strong verbal and written communication. * Proficiency in Microsoft Office Suite, particularly ...
New
Trading Desk Associate Regulatory Analyst
Manhattan, NY · On-site
$125K/yr
Trading Desk Associate Regulatory Analyst (BH-400063) Location New York, United States Sector ... Strong verbal and written communication. * Proficiency in Microsoft Office Suite, particularly ...
New
Trading Desk Associate Regulatory Analyst
Manhattan, NY · On-site
$87K - $125K/yr
Trading Desk Associate Regulatory Analyst Join our client's dynamic team supporting the forefront ... Strong verbal and written communication. * Proficiency in Microsoft Office Suite, particularly ...
Trading Desk Associate Regulatory Analyst
Manhattan, NY · On-site
$87K - $125K/yr
Trading Desk Associate Regulatory Analyst Join our client's dynamic team supporting the forefront ... Strong verbal and written communication. * Proficiency in Microsoft Office Suite, particularly ...
The Clinical Regulatory Writing Associate Director is expected to: * Independently manage clinical regulatory writing activities across a complex portfolio of work. * Author the most complex clinical ...
The Clinical Regulatory Writing Associate Director is expected to: * Independently manage clinical regulatory writing activities across a complex portfolio of work. * Author the most complex clinical ...
The Associate Regulatory Operations Director is responsible for overseeing submission activity for ... Participates in the writing of regulatory processes (SOPs, work instructions, and/or internal ...
The Associate Regulatory Operations Director is responsible for overseeing submission activity for ... Participates in the writing of regulatory processes (SOPs, work instructions, and/or internal ...
The Associate Regulatory Operations Director is responsible for overseeing submission activity for ... Participates in the writing of regulatory processes (SOPs, work instructions, and/or internal ...
The Associate Regulatory Operations Director is responsible for overseeing submission activity for ... Participates in the writing of regulatory processes (SOPs, work instructions, and/or internal ...
Senior Associate, Regulatory Operations
Philadelphia, PA · On-site
$25.94 - $34.43/hr
Overview The Senior Associate, Regulatory Operations is a project-level lead who is responsible for ... Clear, concise technical writing ability Preferred * Experience working on cross-functional teams
Senior Associate, Regulatory Operations
Philadelphia, PA · On-site
$25.94 - $34.43/hr
Overview The Senior Associate, Regulatory Operations is a project-level lead who is responsible for ... Clear, concise technical writing ability Preferred * Experience working on cross-functional teams
The Associate Regulatory Operations Director is responsible for overseeing submission activity for ... Participates in the writing of regulatory processes (SOPs, work instructions, and/or internal ...
The Associate Regulatory Operations Director is responsible for overseeing submission activity for ... Participates in the writing of regulatory processes (SOPs, work instructions, and/or internal ...
Role Summary Rowan Digital Infrastructure is looking for a Senior Associate, Regulatory Affairs ... Strong written and verbal communication skills with experience preparing memos, briefings, or ...
Role Summary Rowan Digital Infrastructure is looking for a Senior Associate, Regulatory Affairs ... Strong written and verbal communication skills with experience preparing memos, briefings, or ...
Associate Regulatory Operations Director (Dossier Planner)
Alameda, CA · On-site
$157K - $222K/yr
Overview The Associate Regulatory Operations Director is responsible for overseeing submission ... Participate in the writing of regulatory processes (SOPs, work instructions, and/or internal ...
Associate Regulatory Operations Director (Dossier Planner)
Alameda, CA · On-site
$157K - $222K/yr
Overview The Associate Regulatory Operations Director is responsible for overseeing submission ... Participate in the writing of regulatory processes (SOPs, work instructions, and/or internal ...
Role Summary Rowan Digital Infrastructure is looking for a Senior Associate, Regulatory Affairs ... Strong written and verbal communication skills with experience preparing memos, briefings, or ...
Role Summary Rowan Digital Infrastructure is looking for a Senior Associate, Regulatory Affairs ... Strong written and verbal communication skills with experience preparing memos, briefings, or ...
The attorneys building it are writing precedent, not following it. This role sits inside that story ... You'll be embedded in the regulatory process: reviewing evidence, developing enforcement theories ...
Quick apply
The attorneys building it are writing precedent, not following it. This role sits inside that story ... You'll be embedded in the regulatory process: reviewing evidence, developing enforcement theories ...
We are now recruiting an Associate Director, Clinical Regulatory Writing (CReW). The Clinical Regulatory Writing team provides expert communications leadership to drug projects and authors ...
New
We are now recruiting an Associate Director, Clinical Regulatory Writing (CReW). The Clinical Regulatory Writing team provides expert communications leadership to drug projects and authors ...
New
Associate Director, Clinical Regulatory Writing (CReW)
Gaithersburg, MD · On-site
$1.3K/wk
We are now recruiting an Associate Director, Clinical Regulatory Writing (CReW). The Clinical Regulatory Writing team provides expert communications leadership to drug projects and authors ...
New
Associate Director, Clinical Regulatory Writing (CReW)
Gaithersburg, MD · On-site
$1.3K/wk
We are now recruiting an Associate Director, Clinical Regulatory Writing (CReW). The Clinical Regulatory Writing team provides expert communications leadership to drug projects and authors ...
New
Associate Director, Clinical Regulatory Writing (CReW)
Gaithersburg, MD · On-site
$1.3K/wk
We are now recruiting an Associate Director, Clinical Regulatory Writing (CReW). The Clinical Regulatory Writing team provides expert communications leadership to drug projects and authors ...
New
Associate Director, Clinical Regulatory Writing (CReW)
Gaithersburg, MD · On-site
$1.3K/wk
We are now recruiting an Associate Director, Clinical Regulatory Writing (CReW). The Clinical Regulatory Writing team provides expert communications leadership to drug projects and authors ...
New
Associate Regulatory Writer information
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$18.99 - $22.95
3% of jobs
$22.95 - $26.90
6% of jobs
$26.90 - $30.86
13% of jobs
$31.38 is the 25th percentile. Wages below this are outliers.
$30.86 - $34.81
20% of jobs
The median wage is $36.35 / hr.
$34.81 - $38.77
19% of jobs
$38.77 - $42.72
9% of jobs
$44.70 is the 75th percentile. Wages above this are outliers.
$42.72 - $46.68
10% of jobs
$46.68 - $50.63
6% of jobs
$50.63 - $54.59
5% of jobs
$54.59 - $58.54
5% of jobs
$58.54 - $62.50
3% of jobs
$18
$39
$62
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Senior Associate Regulatory Affairs
Remote
Full-time
Medical, Dental, Vision, Life, Retirement
Posted 12 days ago
Job description
Regulatory
Job Description
Join Amgen's Mission of Serving Patients
At Amgen, if you feel like you're part of something bigger, it's because you are. Our shared mission-to serve patients living with serious illnesses-drives all that we do.
Since 1980, we've helped pioneer the world of biotech in our fight against the world's toughest diseases. With our focus on four therapeutic areas -Oncology, Inflammation, General Medicine, and Rare Disease- we reach millions of patients each year. Amgen is advancing a broad and deep pipeline of medicines to treat cancer, heart disease, inflammatory conditions, rare diseases, and obesity and obesity-related conditions. As a member of the Amgen team, you'll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives.
Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lay within them, you'll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career.
Senior Associate - Regulatory Affairs
What you will do
Let's do this. Let's change the world. In this vital role you will assist the US Regulatory Leads and the Global Regulatory Team (GRT) in the Regulatory Affairs organization.
- To coordinate and execute US regulatory submissions under the direction of the US Regulatory Lead in compliance with corporate standards and regulatory requirements.
- To manage and execute the preparation, delivery, and electronic archiving of documentation for inclusion in US regulatory submissions
- To assist the Global Regulatory Lead to manage GRT interactions
Key responsibilities include:
- Assist US Regulatory Lead to support local regulatory activities (e.g. IND submissions and agency meetings)
- Provide and maintain CTA/MA documentation support (e.g. initial filings, amendments, and periodic reports) in collaboration with US Regulatory Lead
- Create and maintain product regulatory information and history documents through Amgen systems
- Appropriately archive regulatory documents and agency communications
- Collaborate with CRO's / partners to support site initiation
- Complete regulatory forms to support agency communications
- Participate in GRT to support execution of regulatory strategy
- Coordinate QC of regulatory documentation (e.g. briefing materials)
- Provide primary authorship to routine regulatory correspondence (e.g. annual reports, investigator packages)
- Assist in template development and maintenance
- Respond to specific requests from and communicate relevant issues to GRT
- Actively support regulatory compliance
We are all different, yet we all use our unique contributions to serve patients. The dynamic professional we seek is a self-starter with these qualifications.
Basic Qualifications:
Master's degree
Or
Bachelor's degree and 2 years of Regulatory Affairs experience
Or
Associate's degree and 6 years of Regulatory Affairs experience
Or
High school diploma / GED and 8 years of Regulatory Affairs experience
Preferred Qualifications:
- Strong communication skills - both oral and written
- Ability to understand and communicate scientific/clinical information
- Ability to collaborate with team members to tackle problems and develop a course of action
- Cultural awareness and sensitivity to achieve global results
- Planning and organizing abilities
- Able to prioritize and balance multiple activities
- Ability to deal with ambiguity
- Ability to influence others
As we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well-being. From our competitive benefits to our collaborative culture, we'll support your journey every step of the way.
The expected annual salary range for this role in the U.S. (excluding Puerto Rico) is posted. Actual salary will vary based on several factors including but not limited to, relevant skills, experience, and qualifications.
In addition to the base salary, Amgen offers a Total Rewards Plan, based on eligibility, comprising of health and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work/life balance, and career development opportunities that may include:
- A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts
- A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan
- Stock-based long-term incentives
- Award-winning time-off plans
- Flexible work models where possible. Refer to the Work Location Type in the job posting to see if this applies.
careers.amgen.com
In any materials you submit, you may redact or remove age-identifying information such as age, date of birth, or dates of school attendance or graduation. You will not be penalized for redacting or removing this information.
Application deadline
Amgen does not have an application deadline for this position; we will continue accepting applications until we receive a sufficient number or select a candidate for the position.
Sponsorship
Sponsorship for this role is not guaranteed.
As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other and live the Amgen values to continue advancing science to serve patients. Together, we compete in the fight against serious disease.
Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or any other basis protected by applicable law.
We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.
Salary Range
83,974.90USD -113,613.10 USD