Clinical Trial Trainee Job at Suma Soft
If youโre a recent pharmacy graduate wondering where to begin your professional journey, this opportunity could be just what you need. Suma Soft has opened applications for the role of Clinical Trial Trainee / Oncore Administrator in Pune, specifically targeting freshers from B.Pharm and D.Pharm backgrounds.
Starting a career in clinical research can feel overwhelming at first, especially without prior industry experience. However, opportunities like this make it easier to take that first step. With the healthcare and pharmaceutical research sectors growing rapidly, thereโs an increasing demand for professionals who can support clinical trials and manage data efficiently.

Table of Contents
๐ Job Overview
- Role: Clinical Trial Trainee
- Company: Suma Soft
- Qualification: B.Pharm
- Experience Required: Freshers only
- Location: Pune, Maharashtra
- Salary Range: โน1.5 โ โน2.25 LPA
- Number of Openings: 7
- Industry: Clinical Research
- Employment Type: Full-Time, Permanent
This job is designed for candidates who are eager to learn and want to gain hands-on experience in clinical operations and research workflows.
๐ผ What Youโll Be Working On
One of the best parts of this role is the exposure it offers. As a Clinical Trial Trainee, you wonโt just be doing routine tasks โ youโll get to understand how clinical trials actually function behind the scenes.
Your responsibilities may include:
- Supporting the interpretation of clinical study protocols
- Assisting in creating patient schedules and calendars
- Coordinating activities related to oncology clinical trials
- Helping manage workflows and basic budgeting tasks
- Learning and working on CTMS tools such as Oncore
- Maintaining accurate clinical documentation and records
- Collaborating with different internal teams
- Ensuring that data is accurate and processes are followed correctly
This kind of experience is highly valuable because it combines both technical understanding and practical skills.
๐ Eligibility Criteria & Required Skills
โ Educational Qualification
To apply for this role, you should have:
- A B.Pharm degree (any specialization)
- OR a D.Pharm qualification
Freshers are explicitly encouraged to apply, so prior work experience is not necessary.
๐ก Skills That Can Give You an Edge
While you donโt need advanced knowledge, having some basics will help you stand out:
- A general understanding of clinical trials
- Interest in Clinical Trial Management Systems (CTMS)
- Good communication skills (especially in English)
- Familiarity with MS Excel and MS Office
- Strong attention to detail
- Ability to organize and coordinate tasks efficiently
Employers are usually willing to train candidates, but showing willingness to learn can make a big difference.
๐ฑ Why Freshers Should Consider This Opportunity
Starting your career in the right direction is important, and roles like this can lay a strong foundation. Hereโs why this opportunity is worth considering:
๐น 1. Easy Entry Into Clinical Research
Breaking into clinical research can be difficult without experience. This role is specifically tailored for freshers, making it an ideal starting point.
๐น 2. Exposure to Oncology Research
Oncology is one of the fastest-growing areas in clinical research. Getting early exposure here can open doors to specialized roles later.
๐น 3. Hands-On Experience With CTMS
Learning tools like Oncore (a CTMS platform) gives you a practical advantage and improves your technical skill set.
๐น 4. Real-Time Industry Learning
Instead of just theoretical knowledge, youโll actively work on clinical operations, documentation, and coordination tasks.
๐น 5. Structured Work Environment
Working in a corporate setup helps you develop professional discipline, communication skills, and teamwork abilities.
๐ Career Growth Opportunities
This role is more than just a job โ itโs a stepping stone to a long-term career in the pharmaceutical and clinical research industry.
After gaining experience, you can move into roles such as:
- Clinical Research Associate (CRA)
- Clinical Data Management (CDM) Specialist
- Pharmacovigilance Executive
- Regulatory Affairs Associate
With the right skills and experience, you can also transition into higher-paying and more specialized positions over time.
๐ Tips to Improve Your Chances
If youโre planning to apply, a few simple steps can help you stand out:
- Highlight your pharmacy background clearly in your resume
- Mention any projects, internships, or certifications related to healthcare or research
- Include your technical skills, especially MS Excel
- Show your interest in clinical research through objective statements
- Keep your resume clean, simple, and error-free (How to prepare resume for fresher)
Even if you donโt have experience, a well-prepared resume can make a strong first impression.
๐ How to apply
Interested candidates should apply only through the official company career website using the link provided below.
Important Disclaimer: This job post is shared for informational purposes only, based on publicly available job details. Candidates are advised to verify eligibility, job responsibilities, and application procedures from the official website before applying.
๐ Explore Similar Opportunities
- IQVIA Hiring Associate Trainee Clinical Data Coordinator
- Azurity Pharmaceuticals Hiring Associate โ Drug Safety
- MSD Hiring for CTC
- Glenmarkย hiring for PV Trainee
- Explore more opportunity in clinical research
๐ Career Guide
โFAQ
๐น Who can apply for this Clinical Trial Trainee role?
Candidates who have completed B.Pharm or D.Pharm are eligible to apply. This opportunity is specifically open to freshers, so prior experience is not required.
๐น Is this job suitable for freshers with no clinical research experience?
Yes, absolutely. This role is designed for beginners and includes training and hands-on exposure to clinical trial processes, making it ideal for those starting their careers.
๐น What kind of work will I be doing in this role?
Youโll be involved in tasks like protocol understanding, patient scheduling, documentation, and coordination of clinical trial activities, especially in oncology studies.
