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Syneos Health

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3.9

based on 556 Reviews

1 Syneos Health Regulatory Consultant Job

Senior Regulatory Consultant

inVentiv International Pharma Services Pvt. Ltd

3.9

based on 556 Reviews

5-10 years

₹ 8 - 14L/yr (AmbitionBox estimate)

Kolkata, Mumbai, New Delhi + 4 more

1 vacancy

Senior Regulatory Consultant

Syneos Health

posted 23d ago

Job Role Insights

Flexible timing

Key skills for the job

Pharmacy Customer Service Hospital Administration NDA Medical Writing Recruitment

+ 3 more

Job Description

Senior Regulatory Consultant (EU Market experience)

Job responsibilities

For non-complex and complex submissions, independently fulfill the following responsibilities:

Conduct research of existing product data relative to global or regional regulatory requirements for the preparation of gap analyses, product development plans, and other regulatory submissions.
Contribute to or prepare administrative and technical components of regulatory agency submissions for the IND, for pre-approval submission packages, for product registration applications, and for post-approval maintenance. Prepare briefing packages for regulatory agency meetings or scientific advice and contribute to or support the agency interactions.
Manage and/or operationalize the delivery of day-today regulatory activities for assigned project according to agreed timelines, scope of contract, budgets, and strategies.
Participate as regulatory support on multidisciplinary project teams, which may include clinical and other technical experts, to develop products throughout their life cycle.
Act as a subject matter expert and help the team members with day-to-day trouble shooting activities, presenting solutions to project related problems.
Prepare estimates for conducting regulatory services as part of single or multiple service proposals.
Support meetings with clients to discuss proposals, the status of ongoing projects, and as part of general business development activities.
Ensure compliance with appropriate global regulatory requirements and the company s policies and processes.
Prepare training materials and share best practices in the regulatory area, both internally and externally.
Participate as regulatory support in internal or external project audits.
Participate as regulatory support on internal cross-functional initiatives.
Contribute to the creation and/or maintenance of SOPs and other process related documentation as required.
Provide support in oversight to team members in the execution of their project responsibilities.
Capable of identifying when to ensure line support required to provide additional guidance and direction.
Maintenance of individual training records (Syneos Health or client related) and completion of all designated required training.

Qualifications

What we re looking for

Looking for min 5yrs of experience in CMC authoring and reviewing (specifically Module 3).
Must have EU market experience.
BS or PhD degree, preferably in a science-related field or equivalent experience in science/regulatory/medical writing-related field. Moderate pharmaceutical/medical device related experience.
Demonstrated experience in contributing to the preparation of regulatory submissions including, for example IND, PMA, NDA, MAA, and CTD, including electronic submissions.
Excellent interpersonal / communication skills including excellent written and verbal communication skills.
Excellent customer service skills, with the ability to work both as a team member and independently.
Good quality management skills.
Advanced skills in Microsoft Office Applications.
Ability to interact with staff from multiple departments and offices to establish project standards.
Good initiative, adaptability, and pro-activity.
Strong analytical skills, good attention to detail.
Ability to work concurrently on projects, each with specific instructions that may differ from project to project.
Fluent in speaking, writing, and reading English.

Get to know Syneos Health
Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites and 675,000+ Trial patients.

No matter what your role is, you ll take the initiative and challenge the status quo with us in a highly competitive and ever-changing environment. Learn more about Syneos Health .

Employment Type: Full Time, Permanent

Read full job description

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People are getting interviews at Syneos Health through

(based on 33 Syneos Health interviews)

Job Portal

Referral

Company Website

46%

21%

12% candidates got the interview through other sources.

High Confidence

What Regulatory Consultant at Syneos Health are saying

5.0

Rating based on 2 Regulatory Consultant reviews

Anonymous · Pharmaceutical & Biotechnology in Gurgaon/Gurugram, Haryana

Likes

Syneos has good benefit and the work culture is incredible here. Managers are extremely supportive and doesn't micro manage and takes care about employee work life balance.

Dislikes

Nothing as such as of now

Read 2 reviews