Open To Work
Rahul Brahma
Bengaluru
Summary
I have a combined 4+ years of experience in clinical trial management roles at Labcorp Drug Development and Merck Healthcare. I am an ambitious and results-driven professional with a passion for innovation and excellence. Known for taking initiative, setting and achieving challenging goals, and continuously seeking opportunities for personal and professional growth. Proven track record of delivering high-impact solutions, and exceeding expectations in fast-paced environments. Eager to leverage my skills and enthusiasm to drive success in a dynamic organization.
Overview
5
5
years of professional experience
Work History
Analyst- Clinical Trial Coordinator
Merck Healthcare
10.2022 - Current
- Managing resources and staff list updates.
- Coordinate clinical trial activities, and support Clinical Trial Leads (CTL), PCDL, and TCDL as per project requirements.
- Supporting the CTL, PCDL, and TCDL at the program level using EOS, CML, and other systems as per the task requirement.
- Handle access management with the global team, collaborate with study managers, and trial leads on the CML database system, and develop and maintain effective relationships with vendors.
- Additionally, I work as a Response Coordinator in the VEEVA Vault QMS system, addressing CAPA (Corrective and Preventive Actions), and deviations to resolve issues efficiently.
- Actively involved in SUSAR activities in collaboration with the GPS team, ensuring regulatory compliance, and high standards of clinical research.
- Manage the CSL Dashboard to ensure accurate and up-to-date study details for CSLs.
- Perform Clinical Management Landscape (CML) CTMS data entry and QC, update Trial Team and Vendor Lists, and manage Clinical Site and Investigator data on SharePoint.
- Support study teams with administrative support.
- Create dashboards and system analytics to analyze study metrics, site performance, quality, recruitment, site engagements, etc.
- Support clinical delivery leads in reviewing site visit reports, recruitment activities, and supporting the study to create a newsletter in SharePoint
- Support clinical delivery leads in reviewing site visit reports, recruitment activities.
- Perform START One data entry (portal to register and process regional and local portfolios, maintenance, and QC).
- Track site interaction visits, review DM reports, and support data cleaning.
- Establish data-driven oversight activities, and draft action items to CROs.
- Supporting budget-related activities for regional and global studies. Ensuring compliance with varying regulations and aligning with project goals.
Clinical Project Coordinator
Labcorp Drug Development Corporation
11.2020 - 09.2022
- Ambitious Clinical Project Coordinator with 1 year and 11 months of experience at Labcorp Drug Development Corporation and a proven track record of effective project management and global collaboration.
- In my role at Labcorp, I excelled in managing clinical trial databases, overseeing site updates, and creating new site entries.
- I supported the startup and kit delivery departments, where I collaborated with global teams, including RSC and GSM, to ensure timely project delivery and task completion.
- Additionally, I played a key role in a new process focused on high-priority collaboration between global team and sponsors, demonstrating my ability to manage complex tasks and drive successful outcomes.
- My background reflects a commitment to excellence, a proactive approach to problem-solving, and a passion for advancing clinical research.
Education
Master of Pharmacy -
BIRLA INSTITUTE OF TECHNOLOGY
Ranchi07-2020
Bachelor of Pharmacy -
MAKAUT
West Bengal07-2018
Skills
- Zavacore and Gopher
- Veeva Vault QMS
- Workfront and Trackwise
- EOS and Cenduit
- Clinical analytics systems
- SharePoint and Spotfire
- Resource management tools
- Wingspan and SOW Locator Tool
- Microsoft Office Suite
- Data retrieval techniques
- PubMed and Google Scholar
- Reference management software
Strength/Skills
- I have the ability to collaborate effectively with others toward a common goal; this involves sharing ideas, supporting colleagues, and resolving conflicts constructively
- Organizing and planning how to divide my time between specific activities
- Clearly conveying and receiving messages, whether verbally or in writing
- Analyzing information objectively
- A strong desire and ability to acquire new knowledge and skills
- Demonstrate control and consistency in my actions and habits to achieve goals
- Always try to prevent errors and ensure high-quality work in deliverables
Hobbies and Interests
- Playing Football
- Listening to music
- Watching movies
- Collecting information about Geopolitics and world affairs
- Playing video games
Languages
Bengali
First Language
Hindi
Proficient (C2)
C2
English
Proficient (C2)
C2
References
References available upon request.
Work Preference
Job Search Status
Open to workWork Type
Full TimeSalary Range
₹45000/yr - ₹200000/yrTimeline
Analyst- Clinical Trial Coordinator
Merck Healthcare
10.2022 - Current
Clinical Project Coordinator
Labcorp Drug Development Corporation
11.2020 - 09.2022
Master of Pharmacy -
BIRLA INSTITUTE OF TECHNOLOGY
Bachelor of Pharmacy -
MAKAUT