Are you ready to make your mark in the world of clinical research and life sciences? Novotech, one of the leading global Contract Research Organizations (CROs), is opening doors for talented professionals in India. If your background is in Biometrics, Clinical Data Management, or Clinical Operations, this is your golden ticket to join a global player shaping the future of healthcare.
🌍 About Novotech
Headquartered in Australia, Novotech is a full-service CRO with a strong presence across Asia-Pacific, the US, and now India. Known for delivering quality services in clinical trials, data management, and biometrics, Novotech is committed to improving global health outcomes through cutting-edge research partnerships.
Whether you’re a fresh graduate or an experienced clinical professional, Novotech India’s new hiring drive is offering some of the most in-demand and strategic roles in the pharma ecosystem today.
📢 Open Positions at Novotech India
There are four key roles currently open, each catering to different levels of experience and skillsets across the clinical and regulatory domains:
🧠 1. Biometrics Administrator (Compliance Support Specialist)
Location: India
Experience: 1 to 3 years
Qualification: Bachelor’s in Life Sciences, Computer Science, or Regulatory Affairs
📌 Key Responsibilities:
- Assist in system validation and regulatory compliance under frameworks like GxP, ICH E6, and 21 CFR Part 11.
- Support audit preparation, system qualification, and data integrity reviews.
- Coordinate vendor assessments and track CAPA documentation.
- Maintain validation records and ensure electronic system compliance.
This role is ideal for tech-savvy life science professionals who want to focus on quality systems and digital compliance in a regulated clinical environment.
💻 2. (Senior) Clinical Data Manager
Location: India
Experience: 4 to 10 years
Qualification: Graduate in Clinical Research or Life Sciences
📌 Key Responsibilities:
- Lead the data lifecycle from database design to final lock.
- Ensure processes align with ICH-GCP and GCDMP compliance.
- Perform data validation, cleaning, discrepancy management, and final review.
- Mentor junior data managers, and contribute to SOP enhancement and process documentation.
- Handle financial scope adjustments related to studies.
Perfect for professionals with strong data oversight and leadership skills, especially those interested in process improvement in CRO environments.
👩⚕️ 3. (Senior) Manager – Clinical Operations
Location: India
Experience: Minimum 7 years (including 3+ years in CRO line management)
Qualification: Graduate in Life Sciences or Clinical Research
📌 Key Responsibilities:
- Line management of Clinical Research Associates (CRAs), RSAs, and IHCRAs.
- Conduct performance evaluations, team reviews, and clinical monitoring visits.
- Ensure ICH-GCP compliance, site readiness, and regulatory audit preparation.
- Collaborate with internal BD and trial teams for resource planning and clinical forecasting.
- Provide oversight on clinical SOP adherence and risk mitigation.
This is a leadership-focused role suited for individuals who’ve already navigated the CRO industry and want to lead teams, not just trials.
📊 Why You Should Join Novotech
Novotech isn’t just another CRO — it’s a place where you’ll get:
✅ Work-Life Balance: Stable work hours with a focus on mental well-being
✅ Innovative Projects: Exposure to complex clinical trials and regulatory projects
✅ Growth-Oriented Culture: Career development programs and mentoring
✅ Global Network: Work alongside teams in the US, Australia, and Asia
✅ Corporate Perks: Health insurance, process training, and regular skill upgrades
👥 Ideal Candidates Should Have:
- Strong understanding of clinical trial guidelines and GxP regulations
- Familiarity with tools like EDC systems, SAS, or clinical documentation tools
- Excellent communication skills, especially in remote or multi-site environments
- The ability to analyze protocols, manage teams, and oversee trial metrics
Whether you’re a data nerd, a documentation expert, or a people manager — Novotech has a place for you.
🧩 Day in the Life at Novotech India
Imagine starting your day with a virtual huddle with global teams. You’re either working on cleaning up clinical data discrepancies, preparing for an audit, or reviewing team performance. You might jump on a strategy call with your Australian counterparts or help draft a process improvement plan. Each day is structured yet dynamic, combining clinical precision with innovative thinking.
📑 How to Prepare Before Applying
While the company will handle shortlisting and onboarding professionally, you can stand out by:
- Updating your CV with specific metrics (e.g., number of studies managed, tools used)
- Highlighting your compliance or SOP achievements
- Mentioning remote collaboration experience (especially with international teams)
- Brushing up on ICH-GCP and GCDMP guidelines
💬 Final Words
In the fast-evolving world of clinical research and regulatory science, Novotech is a rising star. If you’re driven by science, committed to compliance, and ready to step into global clinical operations — this is the opportunity you’ve been waiting for.
🔍 Whether you’re just starting out in biometrics or data management, or you’ve been leading clinical teams for a decade — Novotech’s roles are strategically placed to help you grow, lead, and make a difference in the world of clinical research.
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