Job Summary

40 hour per week, remote Clinical Regulatory Writer with demonstrated experience writing clinical pharmacology and bioanalytical reports that go into Modules 2.7.1 and 2.7.2 (will not be writing the modules, just the reports that will go into the modules).

location: Wayne, Pennsylvania

job type: Contract

salary: $80 - 90 per hour

work hours: 9 to 5

education: Doctorate

Responsibilities

Regulatory Writers prepare high quality documentation for regulatory submissions in order to help streamline the regulatory documentation process for our clients.

In this role you will write clinical pharmacology and bioanalytical reports that go into Modules 2.7.1 and 2.7.2.

Qualifications

Required:

At least an MS degree.

Preferred

PhD Degree

skills: Pharmacology, CTD Structure

Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.

At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact [email protected].

Pay offered to a successful candidate will be based on several factors including the candidate's education, work experience, work location, specific job duties, certifications, etc. In addition, Randstad offers a comprehensive benefits package, including: medical, prescription, dental, vision, AD&D, and life insurance offerings, short-term disability, and a 401K plan (all benefits are based on eligibility).

This posting is open for thirty (30) days.

It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.