Joyson B.S., PharmD

Clinical Research Coordinator @ KGK Science Inc.

About

► Joyson is a dedicated healthcare professional in the field of clinical research, bringing 4 years of hands-on experience in clinical operations, pharmacovigilance, and clinical pharmacy. Throughout his career, he has been passionate about contributing to advancements in healthcare and pharmaceuticals. ► He holds a Doctor of Pharmacy (PharmD) degree from Rajiv Gandhi University of Health Sciences, Bangalore, India, and is equipped with comprehensive clinical, hospital, and managed care pharmacy knowledge. CAREER HIGHLIGHTS ‾‾‾‾‾‾‾‾‾‾‾‾‾‾‾‾‾‾‾‾‾‾‾ ★ Recipient of the 'Employee of the Month', 'Employee of the Year', and 'Highest Productivity Achiever of Q2' Awards. ► Managed multiple responsibilities in Clinical Operations, Pharmacovigilance, and Clinical Pharmacy Services including mentorship, training, and as a QC reviewer. TECHNICAL SKILLS ‾‾‾‾‾‾‾‾‾‾‾‾‾‾‾‾‾‾‾‾ ► CTMS (Zavacor) ► EDC ► Argus Safety ► MedDRA ► WHO-DD ► MS Office KEY STRENGTHS ‾‾‾‾‾‾‾‾‾‾‾‾‾‾‾‾‾‾ ► Versatility: He thrives in dynamic environments, adapting to challenges and embracing growth opportunities. ► Determination: His commitment to excellence is evident in his track record of successfully navigating complexity and achieving tangible results. ► Strategic Thinking: He works in a way that meets regulatory standards and enhances efficiency and data accuracy. 📞 Let's Connect! ‾‾‾‾‾‾‾‾‾‾‾‾‾‾‾‾‾‾‾ Joyson is open to potential collaborations and discussing how his skills and experiences align with the goals of your organization. He is excited about contributing to innovative projects and being part of a team dedicated to making a positive impact in the healthcare industry.

Country

City

Canada

Industry

Pharmaceuticals

Skill

Infection Control, Quality check, Electronic Data Capture (EDC), Site Initiation, Subject Screening & Enrollment, Informed Consent Management, Data Collection & Documentation, Vital Signs & Sample Collection, GCP & Protocol Adherence, Pharmacy Assistant and Technician, Research Ethics, Clinical Data Management, Medical Writing, Health and Safety Training, Query Resolution, Medical Chart Review, Document Management, Issue Identification, External Communications, Timelines

Experience

Clinical Research Coordinator

KGK Science Inc.

2025-11 - Present · 11 mos

Ontario, Canada

► Responsible for conducting GCP-compliant clinical visits, administering study assessments, collecting and managing data, and ensuring regulatory adherence. ► Collaborating with cross-functional teams to support participant safety, protocol compliance, and operational efficiency in a fast-paced clinical research environment.

Delivery Associate

GO Logistics Inc.

2024-6 - 2025-11 · 1 yr 6 mos

Ontario, Canada

Worked for DLC4 Amazon Station.

Senior Global Investigator Support & QC Reviewer

Labcorp

2023-1 - 2023-11 · 11 mos

Bengaluru, Karnataka, India

► Responsible for providing technical support to global clinical trial sites, CRAs, principal investigators, and sponsors by collaborating closely with different internal departments like project management, data revision, central labs, etc., by keeping patient safety consistent as a top priority in the day-to-day operations. ► Provided administrative and query resolution responsibilities by ensuring compliance with departmental guidelines and company standards. ► Acted as a mentor and QC reviewer to increase the team's excellence.

Global Investigator Support

Labcorp

2021-5 - 2022-12 · 1 yr 8 mos

Bengaluru, Karnataka, India

► Provided support to clinical trial sites, investigators, CRAs, sponsors, project management team, data revision team, central laboratory, etc. ► Ensured timely delivery of assigned tasks. ► Reviewed the completion of the requested actions and interacted with relevant partners to resolve the issues promptly. ► Retrieved and documented project-related information on time. ► Managed all other duties as assigned.

Junior Data Analyst (Drug Safety)

Cognizant

2020-10 - 2021-4 · 7 mos

Coimbatore, Tamil Nadu, India

Post Marketing Pharmacovigilance Operations for a Multinational Pharmaceutical Company Based in Switzerland. Roles and Responsibilities: ► As Case Intake Member (Intake, Duplicate Check, Book-in) ► As Case Processor – ICSR (Safety Database – Argus v8.1.2) ► As Medical Coder (WHO-DD, MedDRA) ► Adhere to ICH-GCP guidelines, SOPs, Quality requirements, TAT & and accuracy. ► Other Required Drug Safety-related activities. (Introductory Basic Training to new joiners, Background Target Review, etc.)

Clinical Pharmacist

S.S. Institute of Medical Sciences & Research Centre (SSIMS & RC)

2019-8 - 2020-8 · 1 yr 1 mo

Davangere, Karnataka, India

Provided Clinical Pharmacy Services in a 1255-bed super specialty hospital and departments like General Medicine, Pediatrics, Obstetrics and Gynecology, Orthopedics, Hospital Pharmacy, and Drug Information Centre. ► Regular participation in multidisciplinary ward rounds and OPDs. ► Review of treatment charts and critical analysis of the prescription for possible IV incompatibilities, drug interactions, ADRs, and suggesting management strategies in patient care. ► Medical and Medication History Interview. ► Patient counseling to provide information regarding drug profile and lifestyle modification. ► Act as a drug consultant and respond to patients' and all other healthcare professionals' drug-related queries. ► Dispensed medicines as per prescription, dose, dosage form, and expiry date and ensured that medicines were labeled & and supplied correctly.

Research Scholar

S.S. Institute of Medical Sciences & Research Centre (SSIMS & RC)

2018-10 - 2019-3 · 6 mos

Davangere, Karnataka, India

Conducted a Prospective Observational Study on Cost-Effectiveness Analysis of Antihypertensives and Oral Hypoglycemic Agents for a Pharmacoeconomic Evaluation in a 1255-bed Super Specialty Tertiary Care Teaching Hospital.