MP Board Topper List 2026: MPBSE 10th & 12th Toppers Name & Marks (MP Board Topper List 2026) The Madhya Pradesh Board of Secondary Education (MPBSE) has officially released the MP Board Topper List 2026 along with the Class 10th and 12th results. Students can now check the toppers' names, marks, and merit list details online. The topper list highlights the highest-performing students of this academic year and serves as an inspiration for others. 🏆 MP Board 10th Topper List 2026 Here are the top-performing students of Class 10: Rank Student Name Marks 1 Pratibha Singh Solanki 499 2 Abhay Gupta 498 2 Akshara Ghodeshwar 498 3 Himanshi Dhakad 497 3 Shivam Bopche 497 3 Yogendra Singh Parmar 497 3 Nikita Farkase 497 3 Avanish Kumar Nai 497 3 Arjun Singh Rajpoot 497 3 Ananya Verma 497 🏆 MP Board 12th Topper List 2026 Here are the top-performing students of Class 12: Rank Student Name Marks 1 Durga Prasad Rai 494 1 Rambhuvan Vishwakarma 494 2 Vinod Prajapati 493 2 Lalra...
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"SMOConnect Hiring Clinical Research Coordinator (CRC) Trainee in Uduppi, Karnataka | Clinical Research Jobs 2025"
(SMOConnect Hiring Clinical Research Coordinator (CRC) Jobs 2025)
If you’re a Life Science or Pharmacy graduate looking to start a career in clinical research, here’s an excellent opportunity. SMOConnect Clinical Research Services Pvt. Ltd is hiring Clinical Research Coordinator (CRC) Trainees for its site in Uduppi, Karnataka.
This is a full-time, on-site role ideal for fresh graduates who want hands-on exposure to clinical trial operations, regulatory documentation, patient recruitment, and site management under ICH-GCP guidelines.
This job is suitable for candidates searching for:
Clinical Research Coordinator jobs
CRC Trainee openings
Clinical research jobs for freshers
Clinical research jobs in Karnataka
Life Science & Pharmacy fresher jobs
Key Responsibilities:-
As a CRC Trainee, you will assist the clinical research team in daily site operations, including:
• Maintain source documents, CRFs, eCRFs, and Investigator Site File as per ICH-GCP
• Assist in site qualification, initiation, monitoring, and close-out visits
• Manage Investigational Product (IP) storage and temperature monitoring
• Coordinate Ethics Committee (EC) submissions and meetings
• Handle safety reporting within regulatory timelines
• Support patient screening, selection, and recruitment
• Assist with Informed Consent Process (ICF)
• Coordinate with local and central laboratories
• Ensure documentation accuracy and regulatory compliance
Eligibility & Qualifications:-
Educational Qualification
• B.Sc / M.Sc (Life Sciences)
• B.Pharm / M.Pharm
Experience
• Freshers are eligible
Skills Required
• Strong communication and documentation skills
• Basic understanding of clinical trials
• Knowledge of Kannada is mandatory (local patient interaction)
• Ability to work Monday–Saturday (day shift)
✔ Start your clinical research career with real-site exposure
✔ Learn ICH-GCP, site management, and regulatory workflows
✔ Work with experienced investigators and operations teams
✔ Fast-growth environment for fresh graduates
Clear comparison of roles, salary trends, growth prospects, and skillsets — perfect if you’re choosing a pharma career path.
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