All roles

Open role

Regulatory Affairs Associate

Remote · Netherlands Full-time

When our values align, there's no limit to what we can achieve. At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do. Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference. 2-4 yrs yrs in-depth knowledge of Indian regulatory guidelines for clinical trials, including NDCT Rules. Hands-on experience with SUGAM portal for Initial Clinical Trial Application (CTA/iCTA) submissions and amendments. Ability to liaise effectively with global sponsors and cross-functional teams. Prepare necessary documentation, presentations, and briefing materials for SEC meetings Strong understanding of global regulatory expectations and harmonization with Indian requirements. Acquired hands-on expertise in managing and completing clinical trial registrations on the Clinical Trials Registry-India (CTRI) portal. Updated with current Guidelines and Gazette Notifications to give suggestions/comments to respective Regulatory authorities and Govt. regulatory bodies. Working knowledge of India regulatory procedures including adaptability to strict Health Authority and Sponsor timelines for completing submissions Manage timelines for query responses and ensure on-time submission through SUGAM portal or other regulatory platforms. Clear oral and written communication skills Acceptability towards varied cultural mindsets to collaborate efficiently with client counterparts and other internal stakeholders as well Execute and maintain submission delivery plans, submission content plans, and proactively provide status updates to designated stakeholders. Strong communications skills and ability to guide and mentor team members. Ability to work in different time zones Ability to work independently Apply To This Job

More open positions

Sr Manager, Clinical Data Project Mgmt

Work from home Full-time role

Senior Clinical Data Associate job at Sumitomo Pharma in US National

Work from home Full-time role

HIM Clinical Data Analyst, Remote, Health Information Management, FT, 08:30A-5P

Work from home Full-time role

Experienced Data Analyst and Virtual Assistant – Remote Job Opportunities in Healthcare Data Management and Analysis

Work from home Full-time role

Principal Clinical Data Manager

Work from home Full-time role

Remote BCBA (Part-Time, California Only) – $50/hr

Work from home Full-time role

Remote Appointment Setter & Sales Closer — Remote (U.S. Hours)

Work from home Full-time role

US Consumer Marketing Director, Obesity and Related Conditions

Work from home Full-time role

Looking for Remote Adjunct - Criminal Justice Adjunct & Course Developer (Online Applicant Pool) in Bangor, ME

Work from home Full-time role

Virtual Data Entry Clerk - Typist / Full-time (Remote) at careerzynith

Work from home Full-time role

Inventory Buyer

Work from home Full-time role

Cardiovascular Disease Specialist – Seattle South

Work from home Full-time role

[Remote] Mechanical Engineer 2 (NSSS Component Design)

Work from home Full-time role

Online Adjunct Faculty – Criminal Justice

Work from home Full-time role

Sr Claim Examiner- WC

Work from home Full-time role

Business Professional - Program/Project Manager

Work from home Full-time role

Nurse Review Auditor (REMOTE)

Work from home Full-time role

Senior Loan Officer (Remote for CO)

Work from home Full-time role

Corporate Event Planner

Work from home Full-time role

Territory Business Manager - Infinia - Hyderabad HQ

Work from home Full-time role

Pharmacy Tech Support / Call Center Rep (Work from Home)

Work from home Full-time role