Senior Manager, Clinical & Regulatory Medical Writing Job at Lifelancer in Bosto

Job Title: Senior Manager, Clinical & Regulatory Medical Writing Job Location: United States Job Location Type: Remote Job Contract Type: Full-time Job Seniority Level: Mid-Senior level Introduction Our client, a leading mid-sized oncology pharmaceutical company in the United States, is seeking to recruit an experienced and hands-on medical writer to join their team remotely. As senior manager, you'll be an individual contributor overseeing contractors and vendors. Qualifications & Skills Lead authorship: The successful candidate will have extensive experience working as lead authors on Common Technical Document (CTD), Investigational New Drug Application (IND), Biologics License Applications (BLAs), New Drug Applications (NDAs). We are looking for someone with 6+ years' experience. Hands-On Experience: You should be able to demonstrate that your previous work has been mostly hands-on and not just supervisory or managerial responsibilities. Sector Knowledge: Experience within Pharma/Biotech/CROs. Educational Qualification: Ph.D./MD/MS degree holders preferred; however, education can vary based upon prior relevant industry skill set/experience. Salary Expectations Competitive salary package starting at $160,000 per annum. Join our innovative pharmaceutical company today if you meet these qualifications! EOE Statement Specialist Staffing Group is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or veteran status. #J-18808-Ljbffr