Summary
Overview
Work History
Education
Skills
Timeline
Generic

YADAV ALKA RAJKUMAR

CLINICAL TRIAL COORDINATOR
Dehradun

Summary

Dynamic Clinical Research Coordinator with extensive experience at AIIMS, Jodhpur, adept in clinical trial management and patient recruitment. Proven ability to enhance patient safety and data accuracy while fostering collaboration among cross-functional teams. Skilled in informed consent processes and documentation management, with a strong commitment to ethical research practices.

Overview

2
2
years of professional experience

Work History

Clinical Research Coordinator

AIIMS, JODHPUR
12.2024 - Current
  • Followed clinical research protocols and conducted study visits in compliance with ICH/GCP and FDA regulations.
  • Assessed patients'' eligibility criteria following strict adherence to inclusion/exclusion guidelines.
  • Trained new team members on essential clinical research protocols and procedures, promoting a culture of continuous learning.
  • Worked with principal investigator and sponsors to facilitate daily trial activities and comply with research protocols.
  • Managed patient recruitment, informed consent process and data entry to support trial objectives.
  • Coordinated and monitored clinical trial activities to support timely and accurate completion of studies.
  • Gathered, processed, and shipped lab specimens.
  • Collaborated with clinical staff and other healthcare professionals to support clinical trial data accuracy.
  • Maintained accurate and up-to-date case report forms and source documents for traceability.
  • Prepared detailed informed consent documents to clearly communicate risks, benefits, expectations, rights and responsibilities related to participation in clinical trials.
  • Enhanced patient safety by meticulously monitoring and documenting adverse events during clinical trials.
  • Coordinated with cross-functional teams to ensure timely completion of clinical trial milestones.
  • Monitored patient safety throughout clinical trials and reported any adverse events.
  • Screened patient records, databases, and physician referrals to identify prospective candidates for research studies.
  • Prepared and maintained regulatory documents for clinical trial submissions.
  • Facilitated clear communication between principal investigators, sponsors, and study participants for seamless trial execution.

Tutor, Special Needs Students

Home Tution ,India
06.2024 - 11.2024
  • Improved student engagement and understanding by utilizing differentiated instruction techniques within the classroom setting.
  • Participated in regular professional development workshops focused on best practices within special education teaching methodologies and emerging trends in disability support services.
  • Assisted in evaluating student progress through careful observation and data analysis, informing adjustments to instructional techniques as needed.
  • Conducted ongoing assessments of student strengths and weaknesses, adjusting instructional approaches accordingly to maximize each individual''s potential for success.
  • Developed strong relationships with students and their families, fostering open communication channels to address individual concerns and progress updates.
  • Enhanced learning experiences for special needs students by implementing individualized education plans tailored to their unique requirements.
  • Supported students in development of critical thinking skills and perseverance to persist with challenging tasks.
  • Motivated students with accurate feedback and positive reinforcement.

Education

Ph.D. - Cancer Research

SHRI GURU RAM RAI UNIVERSITY
Dehradun, India
04.2001 -

Master of Science - Botany

Uttarakhand Open Univercity
Dehradun, India
04.2001 -

Master of Science - Bioanalytical Science

Guru Nanak Khalsa College of Arts, Science & Commerce
Mumbai
04.2001 -

Bachelor of Science - Chemestry

Guru Nanak College of Arts Science & Commerce
Mumbai, India
04.2001 -

Skills

Research sops understanding

Good clinical practices

Clinical trial management

Clinical research ethics

Documentation management

Research experience

Informed consent process

Trial management

Electronic data capture

Participant screening

Data analysis

Patient recruitment

Research design

Project management

Data management

Medical research

Record keeping

Timeline

Clinical Research Coordinator

AIIMS, JODHPUR
12.2024 - Current

Tutor, Special Needs Students

Home Tution ,India
06.2024 - 11.2024

Ph.D. - Cancer Research

SHRI GURU RAM RAI UNIVERSITY
04.2001 -

Master of Science - Botany

Uttarakhand Open Univercity
04.2001 -

Master of Science - Bioanalytical Science

Guru Nanak Khalsa College of Arts, Science & Commerce
04.2001 -

Bachelor of Science - Chemestry

Guru Nanak College of Arts Science & Commerce
04.2001 -
YADAV ALKA RAJKUMARCLINICAL TRIAL COORDINATOR