MP Board Topper List 2026: MPBSE 10th & 12th Toppers Name, Marks & Merit List PDF

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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. ๐Ÿ† 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 ๐Ÿ† 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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"Clinical Trial Assistant (CTA) Internship at Eccentric Clinical Research, Gandhinagar – Apply Now" ✅

"Clinical Trial Assistant (CTA) Interns Jobs at Eccentric Clinical Research – Gandhinagar, Gujarat"


Eccentric Clinical Research, a rapidly growing Contract Research Organization (CRO) in India, is inviting applications for Clinical Trial Assistant (CTA) Interns at its Gandhinagar, Gujarat facility. This is an excellent opportunity for fresh graduates in Life Sciences, B.Pharm, or M.Pharm who are passionate about building a career in clinical trials, GCP compliance, and regulatory affairs.

Working as a CTA Intern at Eccentric Clinical Research will give you practical exposure to clinical operations, documentation, and regulatory submissions, along with mentorship from experienced professionals.


Key Responsibilities – CTA Intern:-

As a Clinical Trial Assistant Intern, you will:

  • Maintain and update the Trial Master File (TMF/eTMF).
  • Assist with regulatory and ethics committee submissions and documentation.
  • Handle version control, filing, and archival of study documents.
  • Support CRAs and Project Managers during study setup, initiation, monitoring, and close-out activities.
  • Track clinical trial progress using dashboards, trackers, and reports.
  • Coordinate with sites, investigators, and vendors for trial-related activities.
  • Manage distribution and tracking of study supplies and shipments.
  • Ensure compliance with ICH-GCP guidelines, SOPs, and regulatory requirements.
  • Contribute to safety reporting, SAE tracking, audit readiness, and process improvements.

Eligibility Criteria:-

  • Qualification: B.Sc / M.Sc (Life Sciences), B.Pharm, or M.Pharm.
  • Experience: 0–2 years (freshers with internships are encouraged).
  • Skills Required:
    • Knowledge of clinical trial processes, ICH-GCP, and regulatory guidelines.
    • Strong organizational & documentation skills.
    • Proficiency in MS Office (Word, Excel, PowerPoint) and trial management tools.
    • Ability to multitask and work in fast-paced environments.

Why Join Eccentric Clinical Research?

✅ Hands-on experience in clinical operations & trial management.
✅ Training & mentorship from senior CRAs and project managers.
✅ Exposure to regulatory submissions and eTMF systems.
✅ Growth opportunities into CRA and Project Management roles.
✅ Supportive and collaborative work culture.


Job Location:-

  • Gandhinagar, Gujarat, India

Salary Package:-

  • INR 2,00,000 – 3,60,000 per annum (depending on qualifications and performance).

How to Apply?

Interested candidates can apply by sending their updated CV to:
๐Ÿ“ง hr@eccentriccr.com

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