Summary
Overview
Work History
Education
Skills
Extracurricular Activities
Projects
Certification
Languages
Timeline
Work Availability
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Muhammad Hassan

Muhammad Hassan

Houston,TX

Summary

Experienced Clinical Project Manager with over 5 years in clinical research, specializing in trial management, regulatory compliance, and quality assurance. Adept at leading cross-functional teams, managing data systems (iMedidata, RAVE, ARGUS), and ensuring adherence to GCP and ICH guidelines. Proven track record in overseeing protocol amendments, safety reporting, and risk management to deliver high-quality clinical trials on time and within budget. Strong leadership, communication, and problem-solving skills, with a focus on compliance and operational excellence in clinical research environments.

Overview

6
6
years of professional experience
6
6
years of post-secondary education
5
5
Certifications

Work History

Clinical Project Manager

Spring Clinical Research
Houston, TX
8 2019 - Current
  • Lead cross-functional teams to manage and execute clinical trial protocols from start-up to close-out
  • Oversee protocol amendments, revisions, and regulatory documentation to ensure compliance
  • Manage clinical data using Medidata RAVE and ARGUS, ensuring accuracy and timely reporting
  • Develop corrective action plans to mitigate risks and ensure project timelines and budgets are met
  • Coordinate site visits, drug accountability, and electronic data capture (EDC) systems
  • Conduct training for research staff on new protocols, ensuring adherence to study scope and quality.
  • Managed daily operations of 15 person clinic supporting approximately 100 patients per week.
  • Developed strong partnerships with key stakeholders to facilitate smooth handovers during project transitions.
  • Optimized resource allocation across multiple concurrent projects by utilizing advanced scheduling tools.
  • Implemented innovative strategies to improve patient recruitment and retention rates in clinical studies.
  • Collaborated closely with medical experts, investigators, and external partners to ensure accurate data collection in line with research objectives.
  • Facilitated strong relationships between study sites, sponsors, and internal teams through regular updates and effective communication strategies.
  • Mentored junior team members through skill development workshops and one-on-one coaching sessions to enhance their abilities in managing complex projects successfully.
  • Oversaw contract negotiation and vendor selection for clinical projects, securing cost-effective solutions without compromising quality or timelines.
  • Improved clinical trial efficiency by streamlining project management processes and implementing best practices.

Clinical Research Coordinator

Spring Clinical Research
Houston, TX
08.2018 - 07.2019
  • Recruited and screened study participants, ensuring adherence to clinical protocols and requirements
  • Managed patient visits, data collection, and documentation of source data and adverse events
  • Coordinated drug accountability, inventory management, and lab specimen processing
  • Conducted staff training and ensured compliance with study protocols and GCP standards
  • Collaborated with investigators to report protocol deviations and resolve study-related issues
  • Monitored site activities to maintain data integrity and regulatory compliance.
  • Assessed patients'' eligibility criteria following strict adherence to inclusion/exclusion guidelines.
  • 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.
  • Gathered, processed, and shipped lab specimens.
  • Collected data and followed research protocols, operations manuals, and case report form requirements.
  • Collaborated with clinical staff and other healthcare professionals to support clinical trial data accuracy.
  • Prepared detailed informed consent documents to clearly communicate risks, benefits, expectations, rights and responsibilities related to participation in clinical trials.

Education

Doctor of Psychology (PsyD) in Clinical Psychology -

Meridian University
Petaluma, CA
03.2023 - Current

Bachelor of Science in Neuroscience, Minor in Philosophy -

University of Texas At Austin
Austin, TX
08.2018 - 12.2022

Skills

Clinical Research & Compliance

Extracurricular Activities

Football - Junior Varsity, 10, 30 Weeks UIL Current Events - Team Member, 2, 30 Weeks UIL Social Studies - Team Member, 2, 30 Weeks Social Studies National Honor Society - Avid Participant, 3, 30 Weeks Math National Honor Society - Avid Participant, 2, 30 Weeks The Citizens Foundation - Volunteer Coordinator, 2, 4 Weeks Habitat for Humanity - Volunteer, 3, 30 Weeks Clinical Research - Internship, 8, 8 Weeks, 2018

Projects

National Beta Club – President & Co-Founder, 30 Weeks, 3 Boston Leadership Institute – Surgical Program Participant, 3 Weeks, 10 TWC STEM Program – Researcher, 2 Weeks, 40

Certification

Certificate in Compliance Management

Languages

English
Native or Bilingual
Spanish
Limited Working
Urdu
Native or Bilingual
Hindi
Native or Bilingual
Punjabi
Limited Working

Timeline

Doctor of Psychology (PsyD) in Clinical Psychology -

Meridian University
03.2023 - Current

Bachelor of Science in Neuroscience, Minor in Philosophy -

University of Texas At Austin
08.2018 - 12.2022

Clinical Research Coordinator

Spring Clinical Research
08.2018 - 07.2019

Clinical Project Manager

Spring Clinical Research
8 2019 - Current

Work Availability

monday
tuesday
wednesday
thursday
friday
saturday
sunday
morning
afternoon
evening
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Muhammad Hassan