<h2>About Sova Health</h2><div>Sova Health is India’s first full-stack, gut-health and microbiome-focused wellness company, headquartered in Gurgaon. The company is dedicated to solving digestive and metabolic health challenges through science-backed, personalised interventions.</div><div>Built on the belief that gut health is the foundation of overall well-being, Sova Health combines advanced diagnostics, personalised nutrition, targeted supplementation, and expert coaching into a seamless, integrated ecosystem.</div><div> </div><h3>What We Offer</h3><div>Sova Health provides comprehensive, data-driven gut health solutions, including:</div><ul><li>Gut Microbiome and Food Intolerance Testing to deliver deep insights into an individual’s digestion and metabolic profile.</li><li>Personalised probiotics and custom supplement formulations tailored to each person’s unique gut microbiome.</li><li>Expert-led programs offering nutrition guidance, lifestyle recommendations, and ongoing progress tracking.</li><li>Over-the-counter gut-health supplements addressing concerns such as acidity, bloating, constipation, and IBS.</li></ul><div> </div><h3>Our Journey</h3><div>Co-founded by Tanveer Singh and Max Kushnir, Sova Health was established to bring scientific rigor and personalisation to digestive wellness in India.</div><div>Since inception, the company has raised seed funding, demonstrated rapid revenue growth, and built strong consumer traction. Over the years, it has also developed one of India’s most significant microbiome data assets, enabling more precise and culturally relevant health recommendations.</div><div> </div><h3>Our Competitive Edge</h3><ul><li>End-to-end personalisation: Diagnostics → Insights → Custom supplements → Expert coaching</li><li>Proprietary Indian microbiome database for more accurate, region-specific recommendations</li><li>Deep scientific approach leveraging whole-genome analysis and data-driven formulations</li><li>High-touch customer experience with continuous expert support</li><li>Premium, science-first positioning in a market dominated by generic wellness solutions</li></ul><div> </div><div>Sova Health is redefining digestive wellness in India by combining science, technology, and personalisation to deliver measurable, long-term health outcomes.</div>

Sova Health

Project Manager (Clinical Research Associate)
Location: Gurugram
Job Role: Full time
Reporting: Co-founder
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Sova (www.sova.health) is India's first full-stack microbiome health company. We are pioneers in gut health in India, offering probiotic supplements backed by state-of-the-art microbiome diagnostics and therapeutic programs. We are a well-funded startup with investors from Singapore, the US, and India. Working with us, you get to take part in changing people's lives for the better. Every day!
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Why Join Sova?
Sova, in Hebrew, means the feeling of satiety, and this is our promise to our consumers. Be part of a mission-driven company with a vision to add a billion healthy years to the world. Work in a collaborative and innovative environment that values integrity and is driven by ownership. Contribute to changing people's lives for the better every day.
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Job Summary:
We are seeking a highly motivated and detail-oriented Project Manager: Clinical Research/ Senior CRA to join our clinical research team. The CRA will be responsible for the planning, execution, monitoring, and management of clinical trials, ensuring compliance with regulatory guidelines and company protocols. A key aspect of this role includes hands-on data integration, data cleaning, and data analysis and publications to support evidence-based decision-making across the trial lifecycle. This role requires strong analytical skills, scientific rigor, excellent communication, and the ability to collaborate effectively with cross-functional teams.
 
Key Responsibilities:
● Plan, coordinate, and manage clinical trials from site initiation to study close-out.
● Maintain and update trial documentation, including investigator brochures, protocols, and informed consent forms.
● Conduct and document site qualification, initiation, monitoring, and close-out visits (on-site and remote).&nbsp;
● Ensure compliance with Good Clinical Practice (GCP), regulatory requirements, and company policies.
● Support the preparation and submission of regulatory documents to relevant authorities and ethics committees.
● Track and manage trial-related materials, including investigational products and supplies.
● Communicate with investigators, site staff, vendors, and internal stakeholders to facilitate smooth trial operations.
● Organize and participate in clinical team meetings, taking minutes and following up on action items.
● Assist in processing and tracking study invoices, contracts, and budgets.
● Maintain trial master files (TMF) and ensure proper documentation for audits and inspections.
● Validate incoming data against study protocols to confirm completeness, accuracy, and consistency.
● Manage database reconciliation activities, including cross-system data matching and discrepancy resolution.
● Maintain audit trails for all data integrations to support regulatory inspections.
● Ensure Data Integrity and Liability, support in Sponsor/Trial Data collection, cleaning , Analysis and publications.&nbsp;&nbsp;
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Qualifications &amp; Requirements:
● Bachelor’s degree in life sciences, healthcare, or a related field.
● 3-5 years of experience as Project Manager CR/Senior CRA.
● Knowledge of ICH-GCP guidelines, FDA regulations, and other relevant clinical research standards.
● Strong data cleaning skills: query management, edit checks, outlier detection, and database lock processes.
● &nbsp;Attention to detail, analytical mindset, and excellent organisational skills.
● Excellent communication and interpersonal skills.
● Proficiency in G Suite.
● Ability to multitask, prioritize, and work independently in a fast-paced environment.
● &nbsp;Proficiency in at least one data analysis language:SPSS.
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Preferred Qualifications:
● Experience working in a pharmaceutical, biotech, or contract research organization (CRO) setting.
● Certification in clinical research (e.g., ACRP, SOCRA) is advantageous.
● Exposure to real-world data (RWD) platforms or clinical dashboards.
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Benefits:
● Competitive salary and benefits package.
● Opportunities for professional growth and development.
● A collaborative and inclusive work environment.
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Join our team and contribute to groundbreaking research that makes a difference in patients' lives!