I am looking for remote opportunities in Clinical Operations, Project Coordination, Clinical Research, and Clinical Data Management where I can leverage my experience, collaborate with global teams, contribute to meaningful healthcare projects, and continue growing professionally in the life sciences industry.
Dr. Akshay Madhu
@akshaym1
Clinical Research and Project Coordination professional with 3+ years of experience in clinical operations and data management.
What I'm looking for
I am a Clinical Research and Project Coordination professional with 3+ years of experience supporting clinical trials across study start-up, regulatory documentation, clinical data management, and study coordination. I have worked with EDC systems including Medidata Rave, Clinion, and Oracle RDC, managing eCRF data entry, query resolution, SAE reporting support, and ensuring compliance with ICH-GCP guidelines and study protocols.
I am currently working as a Project Coordinator at Clario, collaborating with cross-functional teams to support global clinical projects and ensure timely project execution. Alongside my professional experience, I am pursuing an Online MBA in Pharmaceutical Management from Manipal University Jaipur to strengthen my expertise in healthcare operations, leadership, and project management.
I am passionate about improving clinical research processes, delivering high-quality outcomes, and contributing to innovations that enhance patient care. I am particularly interested in remote opportunities in Clinical Operations, Project Coordination, Clinical Data Management, and Clinical Research within global healthcare and life sciences organizations.
Experience
Work history, roles, and key accomplishments
Coordinated global clinical studies across Germany, Japan, and Malaysia by managing project tracking, stakeholder communication, and documentation to support timelines. Generated project reports and quality metrics using Power BI and QCAT, and managed study records, databases, meeting coordination, and issue resolution while ensuring compliance with internal SOPs.
Senior Clinical Research Coordinator
HCG Cancer Hospital
Nov 2024 - Jan 2026 (1 year 2 months)
Coordinated clinical trial activities including patient screening, study visits, regulatory documentation, Ethics Committee submissions, EDC/eCRF data management, SAE reporting, and query resolution while ensuring ICH-GCP compliance, participant safety, and timely study execution.
Unblinded Clinical Research Coordinator
S4 Research Pvt. Ltd.
Feb 2024 - Nov 2024 (9 months)
Supported clinical trial operations through EDC/eCRF data entry, query management, data review, and regulatory documentation. Collaborated with CRAs, investigators, and data management teams to ensure data accuracy, protocol compliance, timely issue resolution, and adherence to ICH-GCP and study requirements.
Trainee Clinical Research Coordinator
Zenith Clinical Services
Jul 2023 - Feb 2024 (7 months)
Managed EDC/eCRF data entry, data review, and query resolution for clinical studies while ensuring data accuracy and protocol compliance. Collaborated with CRAs, investigators, and data management teams to support timely database updates, issue resolution, and adherence to ICH-GCP and study requirements.
Education
Degrees, certifications, and relevant coursework
Visveswarapura Institute of Pharmaceutical Science (VIPS)
Doctor of Pharmacy, Pharmacy
Doctor of Pharmacy program at Visveswarapura Institute of Pharmaceutical Science (VIPS).
Manipal University
MBA, Pharmaceutical managment
2026 -
Grade: 9.1
Pursuing an Online MBA in Pharmaceutical Management from Manipal University Bengaluru. The program focuses on pharmaceutical business management, healthcare operations, strategic decision-making, marketing, finance, leadership, and project management, strengthening my expertise in the pharmaceutical and clinical research industry.
Tech stack
Software and tools used professionally
Availability
Location
Authorized to work in
Salary expectations
Social media
Skills
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