Clinical Research Regulatory Coordinator
19 hours ago
About Stryde Research We're a Site Management Organization operating 20+ clinical research sites across Dallas-Fort Worth, Houston, Louisiana, New York, and New Jersey. We serve 1.5M+ patients through 100+ specialized clinics with deep expertise in dermatology, rheumatology, cardiology, and general medicine. We're scaling fast—going from 22 to 35+ team members in 2026—and need someone who can keep our regulatory house in order across multiple sites and studies. What You'll Actually Do Prepare and submit IRB applications, amendments, continuing reviews, and reportable events for multiple sites Maintain essential documents: 1572s, delegation logs, training logs, investigator CVs, medical licenses, financial disclosures Track and manage IRB approvals, renewals, and expiration dates across 15+ active studies Coordinate regulatory submissions with sponsors, CROs, and site teams—chase missing documents and keep timelines on track Ensure sites maintain current regulatory binders (paper and electronic) that are audit-ready at all times Manage protocol deviations: documentation, root cause analysis, CAPA implementation, and sponsor reporting Track site training completion and maintain training files per GCP requirements Prepare sites for sponsor audits and FDA inspections—conduct regulatory readiness reviews Communicate regulatory requirements and changes to site coordinators and PIs Support new site initiations: gather essential documents, IRB submissions, and regulatory activation You're the Right Fit If: 2+ years in clinical research regulatory role with multi-site experience Solid understanding of FDA regulations (21 CFR Parts 50, 56, 312), ICH-GCP, and IRB requirements Experience with central and local IRBs (Advarra, WCG, Sterling, Schulman preferred) Comfortable managing competing deadlines across multiple studies and therapeutic areas Detail-oriented enough to catch missing signatures or expired licenses before they become findings Can work independently and proactively—you don't wait to be told what needs renewal in 30 days What Makes You Stand Out: Experience with dermatology, rheumatology, or cardiology trials Background working with SMOs or site networks (you understand coordinating across multiple locations) Familiarity with eTMF systems (Veeva, Florence, Masterfile, or similar) CCRP or ACRP certification showing you're serious about the profession You've supported successful FDA inspections and know what regulators actually look for The Reality Check: This is remote but requires overlap with US business hours for sponsor calls, IRB correspondence, and site coordination. Some weeks you're submitting 5 different IRB amendments. Other weeks you're prepping 3 sites for audits while tracking down expired medical licenses. You'll work across time zones with site teams who are busy with patients and study visits—your job is to make regulatory compliance as painless as possible for them. When a site coordinator emails you at 8pm their time because they just realized an IRB approval expires tomorrow, you need to know exactly what emergency procedures to follow. When a sponsor changes a protocol mid-study, you're coordinating amendments across multiple IRBs with different submission requirements. Compensation & Growth: Competitive salary based on experience. Fully remote from India with flexibility but requires availability during US business hours for critical coordination.
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Clinical Research Regulatory Coordinator
20 hours ago
bangalore, India Stryde Research Full timeAbout Stryde ResearchWe're a Site Management Organization operating 20+ clinical research sites across Dallas-Fort Worth, Houston, Louisiana, New York, and New Jersey. We serve 1.5M+ patients through 100+ specialized clinics with deep expertise in dermatology, rheumatology, cardiology, and general medicine. We're scaling fast—going from 22 to 35+ team...
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Clinical Research Coordinator
22 hours ago
bangalore, India LLRI - Learning Labb Research Institute Full timeWe are seeking a motivated and detail-oriented Clinical Research Coordinator to join our dynamic team. As a Clinical Research Coordinator, you will play a crucial role in the planning, implementation, and coordination of clinical research studies. You will work closely with principal investigators, study participants, and other healthcare professionals to...
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Clinical Operations Manager
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Bangalore, India MS CLINICAL RESEARCH Full timeJob Summary The Clinical Operations Manager will lead and oversee end-to-end clinical study execution across Skin, Hair, and Oral domains. This role is responsible for managing study operations, ensuring compliance with protocols, SOPs, and regulatory guidelines, and coordinating with internal teams, investigators, and sponsors. The candidate will ensure...
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Clinical Trial Coordinator
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Clinical Trial Coordinator
1 week ago
Bangalore, India ClinoGenesis Research Institute Full timeJob Description – Clinical Trial Coordinator (CTC) | Hyderabad About the Role The Clinical Trial Coordinator (CTC) plays a key role in supporting the planning, initiation, execution, and close-out of clinical trials. This role involves coordinating between investigators, clinical research staff, sponsors, and ethics committees to ensure smooth trial...
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Clinical Trial Coordinator
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bangalore district, India ClinoGenesis Research Institute Full time📌 Job Description – Clinical Trial Coordinator (CTC) | Hyderabad About the Role The Clinical Trial Coordinator (CTC) plays a key role in supporting the planning, initiation, execution, and close-out of clinical trials. This role involves coordinating between investigators, clinical research staff, sponsors, and ethics committees to ensure smooth trial...
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Logistics & Customs Clearance Coordinator
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Logistics & Customs Clearance Coordinator
3 weeks ago
Bangalore Division, India MS CLINICAL RESEARCH Full timeJob Description: Logistics & Customs Clearance Specialist Location: Bengaluru Employment Type: Full-Time Experience Level: Ex- Customs Officer/ 2-4 years of Experience Industry: Logistics / Import-Export About Us: MS Clinical Research Pvt Ltd (MSCR) is a pioneering clinical research organization committed to advancing healthcare and life sciences through...
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English Coordinator
1 week ago
Bangalore, India ClinoGenesis Research Institute Full timeJob Description – Clinical Trial Coordinator (CTC) | Hyderabad About the Role The Clinical Trial Coordinator (CTC) plays a key role in supporting the planning, initiation, execution, and close-out of clinical trials. This role involves coordinating between investigators, clinical research staff, sponsors, and ethics committees to ensure smooth trial...
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Information Technology Support Engineer
3 weeks ago
bangalore, India MS CLINICAL RESEARCH Full timePosition: Software Engineer/ IT Support Engineer – Clinical Research Department: IT / Research Technology Location: Indiranagar, Bangalore Employment Type: Full-time/ Consultant Experience : 2-4 years Job Summary We are seeking a Software Engineer / IT Support Engineer to support technology systems used in clinical research and pharmacovigilance...
