Shantanu Deshmukh - CCT, PGDCR

Shantanu Deshmukh - CCT, PGDCR

Clinical Research Coordinator

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location of Shantanu Deshmukh - CCT, PGDCRChhatrapati Sambhajinagar, Maharashtra, India

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  • Timeline

  • About me

    Assistant Project Manager-Clinical Operations at Pristyn Research Pvt Ltd

  • Education

    • Exltech Solutions

      2019 - 2020
      Post Graduation Diploma in Clinical Research Clinical Research A Grade
    • MGM Institute of Health Sciences, Navi Mumbai

      2015 - 2018
      Bachelor of Applied Science - BSc Cardiovascular Technology/Technologist A
  • Experience

    • MGM Medical College And Hospital, Aurangabad

      Jan 2019 - May 2019
      Clinical Research Coordinator

      🌟 Clinical Research Coordinator | MGM Medical College and HospitalPassionate about driving medical breakthroughs and enhancing patient outcomes. As a dedicated Clinical Research Coordinator at MGM Medical College and Hospital, I played a pivotal role in advancing clinical research initiatives and contributing to the realm of healthcare innovation.🔍 Key Contributions:Project Management: Orchestrated the successful execution of 03 clinical trials from initiation to completion, ensuring adherence to protocols, timelines, and regulatory requirements.Patient-Centric Approach: Implemented patient recruitment and retention strategies, prioritizing participant welfare and engagement throughout the trial process.Cross-Functional Collaboration: Fostered seamless communication between research teams, investigators, sponsors, and regulatory bodies, promoting a collaborative environment for successful trial outcomes.🚀 Career Highlights:Led the coordination of 03 Clinical Trials, contributing valuable data to the field and reinforcing the hospital's commitment to cutting-edge medical research.Implemented streamlined processes resulting in efficiency and improvements in clinical trials.Conducted training programs for clinical staff, ensuring a high level of competence and adherence to industry standards. Show less

    • Doclin Clinical Research Services

      Sept 2020 - Jan 2022
      Senior Clinical Research Coordinator

      🌐 Senior Clinical Research Coordinator | Doclin Clinical Research Site ManagementAs a seasoned Senior Clinical Research Coordinator at Doclin Clinical Research Site Management, I played a pivotal role in orchestrating the successful execution of diverse clinical trials. My mission was to bridge the gap between cutting-edge research and patient care, ensuring seamless collaboration between investigators, sponsors, and research teams.💡 Key Competencies:Trial Execution: Spearheaded the implementation of clinical trials from inception to completion, overseeing all operational aspects with meticulous attention to detail.Regulatory Compliance: Ensured strict adherence to regulatory guidelines, maintaining the highest ethical standards throughout the research process.Team Leadership: Led and mentored a dynamic team of research professionals, fostering a culture of excellence, collaboration, and continuous learning.Patient-Centric Approach: Advocated for a patient-centric approach in clinical research, emphasizing the importance of participant well-being and satisfaction.🚀 Career Highlights:Successfully managed 05 clinical trials across therapeutic areas, achieving key milestones within defined timelines and budgets.Collaborated closely with principal investigators, sponsors, and cross-functional teams to streamline processes, resulting in enhanced efficiency and data quality.Implemented innovative strategies for participant recruitment and retention, contributing to the overall success of clinical studies. Show less

    • Pristyn Research Pvt Ltd

      Jan 2022 - Apr 2022
      Clinical Research Associate and Site Operations Manager

      🔍 Clinical Research Professional | Site Operations ManagerDedicated and results-driven Clinical Research Professional with a proven track record as both a Clinical Research Associate (CRA) and Site Operations Manager at Skyline Research CRO. I bring a wealth of experience in overseeing end-to-end clinical trials, ensuring compliance, and optimizing site operations for successful trial execution.💡 Key Strengths:Clinical Research Expertise: Seasoned in conducting and managing clinical trials, ensuring adherence to protocols, regulatory standards, and ethical guidelines.Site Operations Management: Proficient in overseeing site operations, optimizing processes, and fostering strong relationships with investigative sites to enhance efficiency.Regulatory Compliance: Well-versed in navigating complex regulatory landscapes, ensuring all trials are conducted in compliance with applicable regulations.Team Leadership: Successful in leading and mentoring cross-functional teams to achieve project milestones and deliver high-quality results.🚀 Career Highlights:Clinical Research Associate: Managed the initiation, monitoring, and close-out activities for clinical trials, consistently meeting or exceeding project timelines.Site Operations Management: Orchestrated site operations for multiple trials, implementing streamlined processes that resulted in improved efficiency and data quality.Regulatory Success: Led successful regulatory inspections, demonstrating meticulous documentation practices and adherence to compliance standards.🔗 Connect with Me:Let's connect! Whether you're a fellow clinical research professional, an industry collaborator, or someone passionate about advancing healthcare solutions, I look forward to engaging in meaningful conversations and exploring new opportunities. Show less

    • Clinexel Life Sciences Pvt Ltd

      May 2022 - Aug 2023
      Executive Clinical Research

      🔬 Clinical Research Associate | Clinexel Life Sciences AlumnusDedicated Clinical Research Associate with a proven track record at Clinexel Life Sciences, a hub of innovation in healthcare. Over 1.4 years, I played a pivotal role in advancing clinical trials, ensuring adherence to protocols, and contributing to the pursuit of groundbreaking medical solutions.💡 Key Highlights:Protocol Adherence: Meticulously ensured the execution of clinical trials in strict adherence to protocols, regulatory requirements, and industry standards.Site Management: Spearheaded site initiation, monitoring, and close-out activities, fostering strong relationships with investigators and site staff.Quality Assurance: Implemented rigorous quality control measures, resulting in consistently high-quality data collection and reporting.Collaborative Leadership: Worked seamlessly with cross-functional teams, sponsors, and CROs, fostering a culture of collaboration and shared success.Regulatory Compliance: Navigated the complex landscape of regulatory requirements, ensuring all trials under my purview maintained compliance throughout their lifecycle.🚀 Clinexel Experience:During my tenure at Clinexel, I contributed to 01 Global, 02 Phase 1 and 01 Phase 3 Domestic trials including various Sponsor and AICROS Audits, leaving an indelible mark on the organization's commitment to excellence.Thank you for visiting my profile. Looking forward to engaging in insightful conversations and networking with fellow professionals in the clinical research community. Show less

    • Pristyn Research Pvt Ltd

      Aug 2023 - now
      Assistant Project Manager-Clinical Operations

      🌐 Assistant Project Manager | Clinical OperationsAs a dedicated Project Manager in Clinical Operations, I specialize in orchestrating the successful execution of complex clinical trials. With a strong foundation in Clinical Research Industry, I leverage strategic project management to seamlessly integrate people, processes, and technology.💡 Key Competencies:• Strategic Planning: Expertise in developing comprehensive project plans that align with organisational objectives and regulatory requirements.• Cross-functional collaboration: Proven ability to lead and collaborate with multidisciplinary teams, fostering effective communication and synergy across departments.• Risk Mitigation: Adept at identifying potential challenges and implementing proactive solutions, ensuring the timely and cost-effective completion of clinical trials.• Regulatory Compliance: In-depth knowledge of regulatory frameworks, ensuring adherence to compliance standards and guidelines throughout the project lifecycle. Show less

  • Licenses & Certifications

    • Good Clinical Practice

      NIDA Clinical Trial Network
      Jun 2023
    • GCP and Indian Rules and Regulation for Conducting Clinical Trials

      Association of International Contract Research Organization-AICROS
      Aug 2023
    • NIAID Good Clinical Practices Course

      National Institute of Allergy and Infectious Diseases (NIAID)
      Aug 2021
    • Professional Post Graduation Diploma In Clinical Research

      Exceltech Solutions Pvt. Ltd. - India
      Jun 2019