Clinical Research Coordinator Job at Ayati Devices Pvt Ltd Bangalore (Clinical Research Coordinator Job at Ayati Devices Pvt Ltd Bangalore) Introduction Healthcare and life sciences graduates looking to enter the rapidly growing clinical research industry have an excellent opportunity with Ayati Devices Pvt Ltd. The company is currently hiring for the position of Clinical Research Coordinator in Bengaluru, offering candidates the chance to gain practical experience in clinical studies, medical device research, patient coordination, clinical documentation, and healthcare technology projects. This opportunity is particularly suitable for freshers and early-career professionals who want to build a long-term career in Clinical Research, Clinical Operations, Medical Devices, Clinical Trial Management, and Healthcare Analytics. Candidates from healthcare and life sciences backgrounds can gain valuable industry exposure while working alongside experienced investigators and research profe...
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The pharmaceutical and healthcare consulting industry in India is rapidly evolving, with increasing demand for regulatory strategy, global compliance consulting, and life sciences business advisory roles. Vueverse is offering an excellent opportunity for candidates interested in regulatory consulting through its Business Associate – Regulatory Consulting position.
This remote pharma job is suitable for:
B.Pharm and M.Pharm graduates
Biotechnology and Biomedical Engineering professionals
Life Sciences candidates
Freshers with a strong regulatory interest
Early-career pharma professionals (1–3 years experience)
The role provides exposure to:
Global regulatory consulting projects
US, EU, ASEAN, and LATAM markets
Regulatory strategy development
Client management and business consulting
Healthcare compliance systems
This opportunity is ideal for candidates who want to move beyond traditional regulatory affairs roles into strategic consulting and global healthcare advisory careers.
About Vueverse
Vueverse is a healthcare and life sciences consulting organization focused on regulatory consulting, pharmaceutical strategy, and global compliance solutions. The company supports pharma, biotech, and medical device organizations in navigating complex international regulatory environments.
Company Overview
Company Name: Vueverse Industry: Healthcare Consulting / Regulatory Affairs / Life Sciences Headquarters: India (Remote-first global consulting model) Founded: Not publicly disclosed Employees: Small-to-mid scale consulting team (project-based global workforce model) Work Model: Remote & Global Client Operations
Vueverse focuses on:
Regulatory consulting services
Pharma strategy development
Global compliance advisory
Medical device and pharmaceutical submissions
Healthcare business consulting
The company works with international clients across multiple regulated markets.
Job Overview Summary
Vueverse is hiring a Business Associate – Regulatory Consulting to support regulatory strategy development, client consulting, and global compliance projects. The role involves working closely with senior consultants on regulatory submissions, dossier preparation, and business consulting tasks.
This position is a hybrid between:
Regulatory Affairs
Business Consulting
Healthcare Strategy
Client Management
Candidates will gain exposure to international regulatory systems and consulting workflows, making it an excellent career path for pharma professionals looking to enter regulatory consulting and healthcare strategy roles.
Vacancy Details
Job Role: Business Associate – Regulatory Consulting Company: Vueverse Job Type: Full-Time Work Mode: Remote (India-based) Experience Required: 1–3 Years Eligible Candidates: Freshers & Experienced Professionals Industry: Regulatory Affairs / Pharma Consulting / Life Sciences
Job Role Explanation
The selected candidate will support regulatory consulting projects for global pharmaceutical and healthcare clients.
The role includes:
Regulatory strategy development
Dossier preparation support
Client communication
Compliance research
Consulting project execution
This role is not limited to documentation; it involves strategic decision-making, consulting insights, and business-oriented regulatory solutions.
Key Responsibilities Explained
Regulatory Consulting & Project Execution
The candidate will support regulatory consulting activities such as:
Global regulatory pathway assessment
STED and dossier preparation
Labeling and submission support
Regulatory intelligence research
This ensures proper compliance with international regulations.
Client Management & Communication
The role involves direct client interaction, including:
Project coordination
Technical discussions
Progress updates
Regulatory guidance explanation
Strong communication skills are essential.
Business Development Support
The candidate will assist in:
Proposal preparation
Client follow-ups
CRM tracking
Lead management
Upselling opportunities
This makes the role a mix of regulatory and business consulting.
Knowledge Management
Responsibilities include:
Creating regulatory templates
Monitoring global regulatory updates
Developing SOPs
Improving internal consulting processes
Eligibility Criteria
Candidates applying for this Vueverse regulatory consulting job must have:
Educational Qualification
B.Pharm
M.Pharm
B.Tech (Biotechnology / Biomedical Engineering)
Life Sciences Degree
MBA (Optional / Preferred)
Experience Required
1 to 3 years experience preferred
Freshers with strong regulatory aptitude can apply
Skills Required
Technical Skills
Regulatory Affairs knowledge
Global submission understanding
Dossier preparation (STED, CTD awareness)
Pharma compliance knowledge
Regulatory research skills
Scientific documentation
Consulting Skills
Client communication
Analytical thinking
Problem-solving ability
Business consulting mindset
Project coordination
Soft Skills
Strong English communication
Presentation skills
Time management
Team collaboration
Attention to detail
Salary Estimate
Based on current pharma consulting industry trends in India, the expected salary for this role is:
₹5.5 LPA – ₹9 LPA (Approx.)
Salary depends on:
Regulatory experience
Consulting exposure
Communication skills
Project handling capability
Pharma background strength
Why This Job is Unique
This is not a traditional regulatory affairs job. It combines multiple career dimensions:
Regulatory consulting
Business strategy
Client-facing communication
Global healthcare exposure
Pharma compliance advisory
It is ideal for candidates who want to move into:
Pharma consulting careers
Global regulatory advisory roles
Healthcare business strategy
CRO consulting domains
Interview Details
The company has not published official interview rounds publicly. However, the process may include:
Resume screening
HR discussion
Regulatory knowledge assessment
Client communication evaluation
Final managerial round
Required Documents
Candidates should prepare:
Updated CV
Academic certificates
Government ID proof
Experience letters (if applicable)
Internship certificates
Regulatory project details (if any)
Passport-size photograph
Job Location
Location: India (Remote Work) Industry: Pharma Consulting / Regulatory Affairs Work Mode: Fully Remote
Experience Level
1–3 Years preferred
Freshers with strong regulatory interest can apply
Prior consulting or pharma experience is an advantage
Candidates should apply directly through the official LinkedIn job listing.
Frequently Asked Questions (FAQs)
Q1. What is the job role at Vueverse?
The role is Business Associate – Regulatory Consulting.
Q2. Is this a remote job?
Yes, this is a fully remote pharma consulting job in India.
Q3. Who can apply for this role?
B.Pharm, M.Pharm, Biotechnology, Biomedical Engineering, and Life Sciences candidates can apply.
Q4. Is experience required?
1–3 years experience is preferred, but freshers with regulatory knowledge can also apply.
Q5. What is the salary range?
The estimated salary is ₹5.5 LPA – ₹9 LPA.
Q6. What skills are needed?
Regulatory knowledge, communication skills, consulting aptitude, and documentation experience are required.
Final Conclusion
Vueverse’s Business Associate – Regulatory Consulting role is a strong opportunity for pharmacy and life sciences professionals who want to build careers in global regulatory consulting and healthcare strategy.
This role provides exposure to:
International regulatory frameworks
Client-facing consulting projects
Pharma business strategy
Regulatory documentation and submissions
Global healthcare markets
With increasing demand for regulatory consultants in the pharmaceutical industry, this opportunity can serve as a strong career gateway for long-term growth in pharma consulting and regulatory advisory domains.
Disclaimer
Note: Pharma Duniya does not charge any money for job information. Candidates are advised to verify details from the official company website.
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