Clinical Trial Coordinator (Senior Role)

indero
Full Time • Remote
₹22 Lakhs - ₹25 Lakhs
Remote
Posted 50m ago

Clinical Trial Coordinator (Senior Role)

indero

Job description

Want to take your career in clinical research and data analysis to the next level? Learn more about this Clinical Trial Coordinator role at Indero, a remote role in India focused on risk-based clinical trial monitoring.

 Company Description 

Indero (previously Innovaderm) is a dermatology and rheumatology-focused research business. It assists pharmaceutical and biotechnology sponsors in areas like trial design, patient recruiting, clinical monitoring, biometrics, data administration and regulatory services. Indero’s global footprint and cross-regional activities enable it to concentrate on collaboration, innovation, reliability and prompt research delivery to clients globally.

 Job Summary  

The Clinical Trial Coordinator is responsible for the centralised statistical monitoring of clinical trials, which entails examining the accumulated research and operational data for trends, outliers, unusual variability and potential dangers. The role creates study-specific tools, analyses, and monitoring plans in line with essential data and procedures, provides risk assessment and escalation help, advances monitoring automation and coaches colleagues. This is a permanent work-from-home employment in India.

Key Responsibilities

  • Lead the creation of tools, guidelines and statistical analyzes to centrally manage clinical trial data.

  • Develop study-specific monitoring plans based on study risk, critical data and critical processes and develop analytical tools.

  • Detect trends in data quality.

  • Look for probable performance issues in clinical trials, regions and sites.

  • Participate in cross-functional risk assessment meetings on behalf of the central monitoring function and propose appropriate risk reduction actions.

  • Coaching junior team members.

  • Improving monitoring processes through automation.

  • Supporting risk reporting and company-wide efforts.


 Educational Qualification 

  • Bachelor's degree in an area related to clinical research.

  • Minimum 5 years experience in statistics monitoring at central level.

  • At least 10 years of total experience in two or more functional areas (e.g., Clinical Monitoring, Data Management, Drug Safety, Medical Monitoring, Biometrics or Project Management).

  • Extensive knowledge of statistical monitoring, Risk-Based Quality Management (RBQM) and their impact on clinical data integrity.

 Skills Required  

  • Knowledge of clinical trial database systems such as Electronic Data Capture (EDC) systems, Interactive Response Technology (IRT) systems and Clinical Trial Management Systems (CTMS).

  • Experience in clinical data analysis & interpretation of descriptive statistics such as means, medians, significance and confidence intervals.

  • Excellent written and spoken English, able to communicate successfully with internal teams and external customers.

  • Ability to assess clinical data, to detect patterns and outliers and to recognize uncommon variation.

  • Learn about risk-based monitoring strategies and how they relate to clinical trial quality and data integrity.

  • Knowledge of EDC, IRT, CTMS and other clinical trial or data management systems.

  • Advanced knowledge of Descriptive Statistics, Data Review, Reporting Tools and Monitoring Automation.

  • Mentoring of peers, cross-functional teamwork, prioritization of competing needs and straightforward discussion of findings.


 Salary Structure 

The average salary of a Clinical Trial Coordinator is in the range of ₹ 22- 25 Lakhs per year.

 Career Development 

This post also offers opportunity to gain knowledge in areas that include clinical trial analytics, risk based monitoring, data integrity and monitoring automation. Leading cross-functional efforts and mentoring colleagues could develop abilities in technical leadership and strategic decision-making, which would be valuable in future roles in clinical operations, clinical quality management, biometrics and clinical research leadership.

 How to Apply 

  • Go to our job portal and search for the Clinical Trial Coordinator role.

  • Click on the link and fill in the application.

  • Upload your resume and submit your application.

 

 

 

Employment Type: Full Time • Remote
Industry: Healthcare
Role Category: Clinical Research
Application: External (Company Site)

Education

Bachelor's Degree

Key Skills

Clinical ResearchNon Clinical Jobs

Market insights & trends

Salary Insights

The amount of money that gets paid can be different depending on how they have been working, where they live and what kind of job they are doing. Some places pay more than others. Most good jobs include extra money for doing a good job, health insurance and flexible hours. Companies pay high salary to make sure they can get the people they want.

Hiring Trends

The number of jobs for this profile is going up every year. Hospitals and other healthcare companies are looking for people who're good, at their job and can also figure out new problems. They want who can do the work and also think on their feet to deal with the challenges of working in healthcare today.

Frequently Asked Questions

Everything you need to know about the process

Jobslly curates specialized corporate healthcare listings tailored for medical graduates seeking a career pivot. Instead of sifting through general medical job boards, doctors can use our platform to directly access high-paying non-clinical opportunities in Pharmacovigilance, Medical Writing, and Clinical Trial Management with top pharmaceutical companies and CROs. Most MBBS/BDS grads don't realise — clinical background is already enough to get into pharma. The problem is nobody explains this clearly. On Jobslly each listing shows salary range, fresher eligibility, and certifications worth getting before applying. Pharmacovigilance roles for example keep asking for RQAP-GCP. All this is on the listing itself, no separate research needed.
Yes. Jobslly features dedicated filtering for remote and hybrid healthcare roles, which are highly sought after by medical professionals looking for better work-life balance. Doctors can easily track and apply for verified work from home positions, such as Telehealth Consultants, Medical Chart Reviewers, and Drug Safety Associates, directly through the platform Real problem with remote medical jobs — half are fake, half are badly described. You join and realise it's a night shift for a US team nobody mentioned. Jobslly listings show shift timings, contract type, whether company gives equipment or WFH allowance. All upfront before you apply.
Generic job portals often bury specialized clinical roles under thousands of unrelated listings. Jobslly is purpose-built exclusively for the healthcare and health-tech sectors. We provide doctors with targeted career alerts for niche specialties, direct application routes to premium employers in major hubs like Mumbai and Bangalore, and real-time insights into medical salary benchmarks. Salary benchmark is something doctors switching careers genuinely need. No idea what number to quote, quote low, stuck with it forever. Jobslly shows pay ranges — by role, city, experience level. Career alerts are filtered by specialty and location so inbox isn't flooded with irrelevant stuff daily.
To protect medical professionals from recruitment fraud and unverified agencies, Jobslly operates a strictly vetted ecosystem. We exclusively partner with verified employers, prioritizing NABH-accredited hospitals, established health-tech innovators, and recognized multinational pharma brands so you can apply with complete confidence. Fake agencies, ghost listings, upfront fee scams — very common in medical recruitment, especially pharma and international roles. Jobslly doesn't allow unregistered agents on platform at all. Each listing shows actual audit date, not just an old generic verified badge. Suspicious listing — report button is there, compliance checks within 24 hours.
Yes. Backed by the Academically Global network, Jobslly goes beyond domestic job listings by providing access to structured International Placement Programs. We connect ambitious doctors, nurses, and clinical staff with credible, high-paying healthcare contracts in global markets like the UK, Australia, and the UAE, while outlining the necessary credentialing steps. UK needs PLAB, Australia needs AMC, UAE needs DHA or HAAD depending on emirate. Most doctors know this but the full picture — exam pattern, timeline, cost, official links — is scattered everywhere. Jobslly puts the credentialing roadmap directly on each international listing. Academically Global counsellors also available — people who've actually placed Indian doctors in these countries, know exactly where candidates get stuck.
Forget the assumption that only senior doctors make the big money. That's outdated. Right now, some of the best packages in Indian healthcare are going to people you wouldn't expect — Senior Medical Writers, Clinical Data Managers, Pharmacovigilance Specialists working with global pharma firms or CROs. These aren't rare unicorn jobs. They exist, they hire regularly, and the salaries are negotiable in ways hospital jobs rarely are. Most candidates just don't know to look for them.
Not all cities are equal on this front, and applying blindly wastes time. Bangalore is where health-tech and clinical research hiring is concentrated. Hyderabad is pharma country – manufacturing, QC, formulation, R&D. Mumbai and Navi Mumbai handle specialized hospital care, advanced nursing roles, and pharmacovigilance admin, medical writing, policy work all coexist there without one dominating the other. If you're open to relocating, knowing this upfront changes which jobs you even bother applying for.
Both. That's the honest answer. Legitimate remote roles in healthcare have existed long before anyone started calling things "hybrid." Medical Coders, Pharmacovigilance Associates, Telehealth Coordinators, Freelance Medical Writers — these positions have been hiring remotely for years through companies that are very much real. The fake ones almost always have one thing in common: they ask for money. Registration fees, document processing charges, security deposits — whatever the label, it's a scam. No actual employer takes money from a candidate before they join. That rule holds without exception.
EMR platforms, digital documentation tools, data tracking systems, AI-assisted reporting software. These aren’t “nice to have” anymore. They’re baseline. Clinical Knowledge is still the foundation but walking into an interview unable to navigate the systems the team uses daily is a problem. Candidates who are already familiar with these tools don’t need to be trained from scratch, and that matters when hiring managers are comparing two otherwise similar profiles.
Short answer: yes, and it's happening constantly. Long answer: it depends on what you want. If structured hours, no emergency calls, and a salary that doesn't plateau after three years sound appealing — corporate healthcare is worth your attention. Medical Writing, Drug Safety Review, Insurance Auditing, Health-tech Program Management — these roles specifically want people who understand clinical realities. A nursing degree or MBBS isn't a handicap here. It's often the reason you get the interview.