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Regulatory / Sr Regulatory Associate (Module 1, Regulatory Submission)

2-4 years
₹7,00,000 - ₹12,00,000 per annum
10 May 23, 2025
Job Description
Job Type: Full Time Education: BA/BS Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Here is the complete job description including an estimated salary for the Regulatory / Sr Regulatory Associate (Module 1, regulatory submission) role in India:


Regulatory / Sr Regulatory Associate (Module 1, regulatory submission)

Updated: May 9, 2025
Location: India-Asia Pacific - IND-Home-Based
Job ID: 25003476

Description
Syneos Health is the only fully integrated biopharmaceutical solutions organization purpose-built to accelerate customer success. We lead with a product development mindset, seamlessly connecting our capabilities to add high-value insights to speed therapies to patients and provide practical value to help our customers achieve their objectives.

Our Clinical Development model brings the customer and the patient to the center of everything that we do. We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to work with, but to make us easier to work for.

Whether you join us in a Functional Service Provider partnership or a Full-Service environment, you’ll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals. We are agile and driven to accelerate the delivery of therapies, because we are passionate to change lives.

Discover what our 29,000 employees, across 110 countries already know:
WORK HERE MATTERS EVERYWHERE

Why Syneos Health

  • We are passionate about developing our people, through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program.

  • We are committed to our Total Self culture – where you can authentically be yourself. Our Total Self culture is what unites us globally, and we are dedicated to taking care of our people.

  • We are continuously building the company we all want to work for and our customers want to work with. Why? Because when we bring together diversity of thoughts, backgrounds, cultures, and perspectives – we’re able to create a place where everyone feels like they belong.

Job Responsibilities

Essential Functions
For non-complex submissions, independently fulfill the following responsibilities. For complex submissions, fulfill the following responsibilities under supervision and with guidance from more senior regulatory colleagues:

  • Interpret health authority approval letters and update registration data for marketed and investigational approvals.

  • Ability to independently and accurately process the intake, archival and extraction of data from health authority correspondence including adding questions and commitments into tracking database, archiving documentation correctly, linking content to the correct submission and application data, and highlighting critical regulatory milestones.

  • Responsible for ensuring data required for assigned program team is entered into the RIM system, is associated with the correct applications and is correct to build content plans and create registration records.

  • Coordinates data review with data owners, in accordance with reporting timelines and due dates.

  • Highlights non-compliance and quality issues to the Regulatory Information Management team.

  • Undertakes information processing activities with extremely high reliability at high quality and in tight timelines according to standard processes and operating procedures.

  • Undertake project specific activities with minimal supervision from senior colleagues within cost and time estimates/contracts.

  • Attends client meetings as needed and builds client relationship in support of projects and deliverables.

  • Systematically reviews Regulatory Associates or other Senior Associate’s work, performance, and productivity tracking, coordinating with project manager and director for coordination of the project.

  • Assists in training and mentoring of team members depending upon project requirements.

  • Maintenance of individual training records (Syneos Health or client related) and completion of all designated required training.

Qualifications

  • 2 - 4 years of regulatory experience.

  • Minimum 2 years of Veeva vault and RIMS experience.

  • BS/BA degree or equivalent practical experience.

  • Experience in a work-related area preferred.

  • Excellent interpersonal / communication skills.

  • Advanced skills in Microsoft Office Applications.

  • Strong analytical skills.

  • Ability to work independently and to understand and carry out detailed instructions.

  • Ability to interact with staff from multiple departments.

  • 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.

Additional Information:
Tasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description. The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above. Further, nothing contained herein should be construed to create an employment contract. Occasionally, required skills/experiences for jobs are expressed in brief terms. Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees. The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job.

Salary Estimate: ₹7,00,000 - ₹12,00,000 per annum (depending on experience and location within India)