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CRC Job Openings at SkyCraper Clinical Research Solutions | Apply on Biotecnika
Looking to build a career in clinical research? Explore the latest CRC Job Openings at SkyCraper Clinical Research Solutions | Apply on Biotecnika and take the next step toward a rewarding role in clinical trial coordination. These opportunities are ideal for life science graduates seeking hands-on experience in site management, regulatory compliance, and ICH-GCP–aligned clinical research operations.
Job Title: Clinical Research Coordinator (CRC)
Company Name: SkyCraper Clinical Research Solutions
Experience: Minimum 1 year
CTC: 3 – 5LPA
Number of vacancies: above 1
Rounds of interview: 2 rounds Virtual
Qualification: B.Sc / M.Sc in Life Sciences, Biotechnology, Clinical Research, or related disciplines
Location: Ahmedabad, Gujarat
Job Summary:
SkyCraper Clinical Research Solutions is looking for a motivated and detail-oriented Clinical
Research Coordinator (CRC) to join our growing team in Ahmedabad. The ideal candidate
will have hands-on experience in clinical trial coordination and will be responsible for
supporting site operations, ensuring regulatory compliance, and maintaining ICH-GCP
standards across clinical studies.
Key Responsibilities:
• Support end-to-end clinical trial activities from study initiation to close-out
• Act as the primary point of contact for investigators, sponsors, CROs, and internal
teams
• Assist in patient recruitment, screening, enrollment, and follow-up activities
• Maintain and regularly update Trial Master File (TMF) and Investigator Site File (ISF)
• Ensure strict compliance with ICH-GCP guidelines, SOPs, and applicable regulatory
requirements
• Prepare, organize, and manage regulatory submissions and essential study
documentation
• Track study progress and ensure adherence to study protocols, timelines, and
milestones
• Support CRA monitoring visits, internal audits, and regulatory inspections
• Coordinate investigational product accountability and biological sample handling, if
applicable
• Ensure effective communication between site staff, sponsors, and CRO teams
• Document, report, and follow up on Adverse Events (AEs) and Serious Adverse Events
(SAEs) as per protocol timelines
• Apply strong organizational, multitasking, and communication skills to support
smooth site operations
• Maintain a high level of accuracy, attention to detail, and a collaborative team-
oriented approach
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