Senior Associate, Regulatory Writer
Senior Associate, Regulatory Writer
Amgen
Job description
Looking to start a career in writing? Check out this Senior Associate, Regulatory Writing position at Amgen located in Hyderabad.
Company Description
Amgen is focused on unlocking the power of biology to help people who are dealing with illnesses. The company finds, creates, makes and provides medicines for humans using tools like advanced human genetics. Amgen concentrates on areas where there is a need for better medical care, using its strong knowledge of making biologics to improve health results. Since 1980, Amgen has been a leader in biotechnology. Has become one of the top independent biotech companies in the world.
Job Summary
This job involves writing and editing regulatory documents, such as clinical study reports and investigator brochures. As a Senior Associate, you will take part in reviews of documents that involve teams and help manage the time frames for submitting documents to regulators. Your tasks will include writing protocols, informed consent forms and simple summaries. The role also requires working with project teams and other people who write regulatory documents.
Key Responsibilities
Edit simple regulatory documents, including protocols and investigator brochures.
Create documents on your own, such as informed consent forms and changes to documents.
Join team activities that require gathering input from authors and reviewers.
Help with the process of reviewing documents across teams, including sorting comments and attending meetings.
Assist in creating tables and figures inside the text for documents.
Keep track of the time frames for creating documents while making sure they follow the rules.
Work with project teams to keep up with progress and help with document reviews.
Use the required tools and technology for writing.
Go to meetings with teams to share and collect important project information.
Follow the rules, templates and writing style guides for writing at every step.
Educational Qualification
Doctorate with 2 years of experience.
Master's with 4 to 6 years, Bachelor's with 6 to 8 years, or a similar mix of education and experience.
Skills Required
Good understanding of the rules of writing and document standards.
Good knowledge of ICH and GCP rules that are related to submitting documents.
Strong writing & editing skills.
Ability to understand and explain data clearly.
Strong focus on details. Making sure all documents are consistent.
Good teamwork skills to work with teams.
Ready to learn and use writing tools and platforms.
Salary Structure
The pay for a Senior Associate in Regulatory Affairs or Writing at Amgen usually ranges from ₹14.5 Lakhs to ₹17.5 Lakhs every year in India.
Career Development
This job gives experience in writing global regulatory documents within a top biotech company. Amgen also helps with long term growth through guidance, training and chances to move into complex regulatory writing jobs.
How to Apply
Visit our job portal and search for the Senior Associate, Regulatory Writer role - Amgen.
Click on the job posting to read all the details, about the job.
Fill in your details. Upload your updated resume.
Send your application.
Education
Postgraduate Degree (Master's/PhD)
Key Skills
Market insights & trends
Salary Insights
The amount of money that gets paid can be different depending on how they have been working, where they live and what kind of job they are doing. Some places pay more than others. Most good jobs include extra money for doing a good job, health insurance and flexible hours. Companies pay high salary to make sure they can get the people they want.
Hiring Trends
The number of jobs for this profile is going up every year. Hospitals and other healthcare companies are looking for people who're good, at their job and can also figure out new problems. They want who can do the work and also think on their feet to deal with the challenges of working in healthcare today.