
5001 - 10000 employees
Founded 2001
💊 Pharmaceuticals
🧬 Biotechnology
⚕️ Healthcare Insurance
💰 $8.6M Venture Round on 2020-10
Pharmaceuticals • Biotechnology • Healthcare Insurance
ProPharma is a leading research consulting organization in the life sciences industry. The company specializes in providing custom solutions across the full product lifecycle, from early discovery to post-market monitoring. ProPharma's services include regulatory sciences, clinical research solutions, quality and compliance services, pharmacovigilance, medical information, and R&D technology. Known for its deep domain expertise, ProPharma assists clients in the pharmaceuticals, biotechnology, and medical device sectors with regulatory support, clinical development, and quality management. ProPharma's global team supports a wide range of therapeutic areas including oncology, cardiovascular, and rare diseases, among others, ensuring effective and efficient delivery of life-saving therapies.
🔥 3 minutes ago
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5001 - 10000 employees
Founded 2001
💊 Pharmaceuticals
🧬 Biotechnology
⚕️ Healthcare Insurance
💰 $8.6M Venture Round on 2020-10
Pharmaceuticals • Biotechnology • Healthcare Insurance
ProPharma is a leading research consulting organization in the life sciences industry. The company specializes in providing custom solutions across the full product lifecycle, from early discovery to post-market monitoring. ProPharma's services include regulatory sciences, clinical research solutions, quality and compliance services, pharmacovigilance, medical information, and R&D technology. Known for its deep domain expertise, ProPharma assists clients in the pharmaceuticals, biotechnology, and medical device sectors with regulatory support, clinical development, and quality management. ProPharma's global team supports a wide range of therapeutic areas including oncology, cardiovascular, and rare diseases, among others, ensuring effective and efficient delivery of life-saving therapies.
• Serve as point of contact for day-to-day Site communications, document submissions and activity coordination • Support pre-screening, screening and recruitment activities, as assigned • Responsible for subject re-consenting, acquiring medical records, conducting protocol activities, as directed by the Principal Investigator • Perform data-entry, evaluate and respond to system queries and monitor clinical databases as assigned • Establish and maintain timely Site communication as assigned • Maintain documentation which complies with IRB/FDA policies • Assist with study closeout • Assist site with other study-related activities as directed • Other duties as assigned.
• Minimum 2 years of experience as a Study Coordinator • Fluent in both Tamil and English • Ability to manage technology and web-based research platforms on PC (Microsoft OS) laptop in the remote workspace • Study Team experience is ideal • Critical thinking skills • Strong communication Skills (verbal and written) • Ability to work independently, and collaboratively with other CSCs to delegate tasks as needed • Current knowledge of and the ability to apply ICH / GCP and applicable regulations and guidelines • Competent in the application of standard business procedures including but not limited to SOPs, global regulations • Well organized and able to multitask.
• We celebrate our differences and strive to create a workplace where each person can be their authentic self. • We are committed to diversity, equity, and inclusion. • Employees are encouraged to unleash their innovative, collaborative, and entrepreneurial spirits. • With a holistic approach as an Equal Opportunity Employer, we provide a safe space where all employees feel empowered to succeed.
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