Are you looking for an opportunity to advance your career in clinical research? ๐ฌ Med Express Clinical Research Solutions Private Limited is reportedly hiring for the position of Clinical Research Coordinator (CRC) in Chhatrapati Sambhajinagar (Aurangabad), Maharashtra.
This opportunity may be suitable for candidates with experience in clinical research coordination, clinical trials, patient recruitment, and study documentation. Professionals with previous oncology clinical trial experience may have an additional advantage.
Candidates interested in working in clinical research can explore the job details, eligibility requirements, key responsibilities, and application process below.
Important: The recruitment information in this article is based on the details provided for this vacancy. Candidates should verify the current availability of the position and application instructions with the employer before applying.
Med Express Clinical Research Recruitment 2026: Job Overview
| Job Details | Information |
|---|---|
| Company Name | Med Express Clinical Research Solutions Private Limited |
| Job Position | Clinical Research Coordinator (CRC) |
| Job Category | Clinical Research Jobs |
| Job Location | Chhatrapati Sambhajinagar (Aurangabad), Maharashtra |
| Qualification | Relevant degree in Pharmacy, Life Sciences, Nursing, or a related discipline |
| Experience | 1+ years |
| Preferred Experience | Oncology clinical trials |
| Employment Type | Full-time / Permanent, as stated in the vacancy information |
| Joining Preference | Immediate joiners preferred |
| Application Mode | |
| HR Email | go in how to apply |
| Salary | Not specified |
| Application Deadline | Not specified |
About Med Express Clinical Research Solutions Private Limited
Med Express Clinical Research Solutions Private Limited is the organization named in this recruitment announcement.
Clinical research organizations and clinical trial sites support the development and evaluation of medical treatments by coordinating study activities, maintaining trial documentation, and following applicable ethical and regulatory requirements.
Clinical Research Coordinators play an important role in coordinating activities between investigators, trial participants, sponsors, and other members of the research team.
Candidates considering this opportunity should review the employer’s requirements and confirm the job details directly before submitting personal information.
Clinical Research Coordinator (CRC) Job Responsibilities
A Clinical Research Coordinator supports the day-to-day activities involved in conducting clinical trials. The exact responsibilities depend on the study protocol, therapeutic area, and requirements of the clinical trial site.
Typical responsibilities may include the following.
1. Patient Recruitment and Coordination
- Assist the principal investigator and study team with participant screening and recruitment.
- Coordinate participant appointments and clinical trial visits.
- Explain study procedures and visit schedules to participants as authorized by the study team.
- Support the informed consent process in accordance with approved procedures and applicable requirements.
- Maintain communication with participants regarding scheduled study visits and follow-up activities.
2. Clinical Trial Documentation
- Maintain accurate clinical trial records and source documentation.
- Assist with completing case report forms (CRFs) and electronic case report forms (eCRFs).
- Maintain essential study documents and support document filing activities.
- Assist with resolving data queries within the required timelines.
- Ensure that study documentation is maintained according to the protocol and applicable standard operating procedures.
3. Regulatory and Ethical Compliance
- Follow the study protocol, Good Clinical Practice (GCP) requirements, and applicable regulatory procedures.
- Assist with preparing documents for Institutional Ethics Committee (IEC) submissions and approvals, as applicable.
- Support preparation for sponsor monitoring visits, internal audits, and regulatory inspections.
- Report safety information to the investigator and relevant study personnel according to established procedures.
- Maintain participant confidentiality and protect sensitive clinical information.
4. Investigational Product and Sample Management
Depending on the assigned study, responsibilities may include:
- Supporting investigational medicinal product (IMP) accountability and documentation.
- Monitoring storage conditions and maintaining required records.
- Coordinating biological sample collection, processing, storage, and shipment according to the protocol.
- Ensuring that study materials are handled according to approved procedures.
5. Coordination With the Clinical Research Team
- Work with principal investigators, sub-investigators, research nurses, laboratory personnel, and other study staff.
- Coordinate study-related activities and follow-up visits.
- Communicate operational issues to the appropriate team members.
- Support timely completion of assigned study activities.
Note: These are typical CRC responsibilities, not a verified list of duties specific to this employer.
Eligibility Criteria for Med Express CRC Recruitment 2026
Candidates interested in this Clinical Research Coordinator vacancy should review the following requirements.
Educational Qualifications
Relevant educational backgrounds may include:
- B.Pharm or M.Pharm
- B.Sc. or M.Sc. in Life Sciences
- Biotechnology
- Nursing
- Other relevant clinical or healthcare disciplines
The exact accepted qualifications should be confirmed with the employer.
Work Experience
According to the supplied vacancy information, candidates should have at least one year of relevant experience.
Experience in roles such as the following may be relevant:
- Clinical Research Coordinator
- Clinical Trial Coordinator
- Clinical Research Site Coordinator
- Clinical Research Associate with relevant site-level experience
Candidates should ensure that their actual experience matches the employer’s requirements.
Oncology Clinical Trial Experience
Previous experience in oncology clinical trials is preferred according to the supplied information.
Candidates with oncology experience may have worked with patient screening, protocol-specific assessments, study documentation, adverse event reporting, and scheduled follow-up visits.
However, candidates without oncology experience should not assume they are ineligible if they otherwise meet the stated requirements. Confirm the employer’s expectations before applying.
Skills Required for a Clinical Research Coordinator
Applicants can strengthen their applications by highlighting relevant knowledge and practical experience in the following areas.
1. Good Clinical Practice (GCP): Understanding ethical clinical trial conduct and participant protection.
2. Clinical Trial Documentation: Experience with source documents, CRFs, eCRFs, and essential study files.
3. Regulatory Awareness: Familiarity with applicable Indian clinical research regulations and ethics committee procedures.
4. Patient Coordination: Ability to communicate clearly with study participants and coordinate scheduled visits.
5. Attention to Detail: Accuracy in clinical records, study documentation, and data entry.
6. Time Management: Ability to manage multiple study activities and meet documentation deadlines.
7. Teamwork: Ability to coordinate with investigators, research staff, and other clinical trial stakeholders.
Candidates should mention only those skills and certifications they genuinely possess.
Why Consider a Career as a Clinical Research Coordinator?
A CRC position can provide valuable experience for professionals interested in clinical research and clinical trial operations.
Potential career-development benefits include:
- Practical Experience: Exposure to the daily operations of clinical studies.
- Research Documentation Skills: Opportunities to develop experience with study records and data collection.
- Regulatory Knowledge: Greater familiarity with GCP and clinical trial procedures.
- Therapeutic Area Exposure: Experience supporting studies in areas such as oncology, depending on the assigned projects.
- Career Progression: Relevant experience may support future applications for senior CRC, site management, or other clinical research positions, depending on qualifications and performance.
These are general career considerations rather than guaranteed benefits offered by the employer.
Med Express Clinical Research Jobs 2026: Salary Details
The salary for this Clinical Research Coordinator vacancy has not been provided in the supplied recruitment information.
Compensation may depend on the candidate’s qualifications, relevant experience, therapeutic area exposure, and the employer’s salary structure.
Candidates can request details about the following during the recruitment process:
- Monthly salary or annual CTC
- Other compensation or benefits, if applicable
- Working hours and weekly schedule
- Probation period, if any
- Leave policy
- Joining date and employment terms
Avoid relying on unverified salary figures when evaluating this opportunity.
How to Apply for Med Express Clinical Research Coordinator Jobs
Interested candidates who meet the stated eligibility requirements can use the email application method provided in the vacancy information.
Application Email: hr@mecrsindia.com
Step 1: Prepare Your Updated Resume
Create a professional CV that clearly highlights your educational qualifications, clinical research experience, and relevant skills.
Include the following information:
- Full name and contact details
- Educational qualifications
- Total relevant work experience
- Current or previous employer
- Clinical trial experience
- Therapeutic areas, including oncology if applicable
- Knowledge of GCP and clinical trial documentation
- Relevant certifications
- Current location and notice period
Step 2: Write a Professional Application Email
Use a clear subject line that identifies the position.
Suggested email subject:
Application for Clinical Research Coordinator (CRC) โ [Your Full Name]
In the email body, briefly introduce yourself, mention your relevant experience, and explain why you are applying.
Step 3: Attach Your Resume
Attach your updated resume in PDF format. Check that the document opens correctly and that your contact information is accurate.
Step 4: Send Your Application
Send your application to:
If you are available to join immediately, mention your availability in the email, provided this is accurate.
Sample Email for CRC Job Application
Subject: Application for Clinical Research Coordinator (CRC) โ [Your Full Name]
Dear Hiring Team,
I am writing to express my interest in the Clinical Research Coordinator position at Med Express Clinical Research Solutions Private Limited in Chhatrapati Sambhajinagar.
I have [number of years] of experience in [clinical research/clinical trial coordination/relevant field] and hold a [your qualification] degree. My experience includes [mention relevant responsibilities, therapeutic areas, or clinical research skills].
I am interested in this opportunity and would appreciate the chance to discuss how my qualifications and experience align with your requirements.
Please find my updated resume attached for your consideration.
Thank you for your time.
Kind regards,
[Your Full Name]
[Your Contact Number]
[Your Current Location]
[Your Notice Period]
Before applying, confirm that the vacancy is still open and that the email address is correct.
Frequently Asked Questions (FAQs)
1. What is the position offered by Med Express Clinical Research Solutions?
The supplied recruitment information identifies the position as Clinical Research Coordinator (CRC).
2. Where is the CRC job located?
The stated location is Chhatrapati Sambhajinagar, formerly known as Aurangabad, in Maharashtra.
3. How much experience is required?
The supplied information specifies at least one year of relevant experience.
4. Is oncology experience mandatory?
Oncology clinical trial experience is described as preferred. Candidates should confirm the final eligibility requirements with the employer.
5. Which qualifications are suitable for this position?
Relevant degrees may include Pharmacy, Life Sciences, Biotechnology, Nursing, or related clinical disciplines. The employer should confirm the accepted qualifications.
6. How can candidates apply for this vacancy?
According to the supplied information, candidates can email their resumes to hr
7. What is the salary for this CRC position?
The salary has not been specified in the available vacancy information. Candidates should contact the hiring team for details.
8. Is this a work-from-home opportunity?
The supplied information does not confirm whether remote work is available. Candidates should ask the employer about the work arrangement. The stated location is Chhatrapati Sambhajinagar.
9. Are freshers eligible for this vacancy?
The supplied information specifies at least one year of relevant experience. Freshers should confirm directly with the employer whether applications without prior experience will be considered.
10. What is the last date to apply?
An application deadline has not been provided. Interested candidates should verify whether the position is still open before applying.
Final Thoughts
The Clinical Research Coordinator vacancy listed for Med Express Clinical Research Solutions Private Limited may be worth exploring for professionals with relevant clinical research experience who are looking for opportunities in Chhatrapati Sambhajinagar, Maharashtra.
Candidates with at least one year of relevant experience, strong documentation skills, and knowledge of GCP may find this role relevant to their career goals. Oncology clinical trial experience may be an advantage.
Before submitting your application, verify the vacancy details, salary, eligibility criteria, and application email with the employer.
๐ Recommended Online Course for Clinical Research Professionals & How to apply
Are you looking to strengthen your understanding of clinical research and clinical trial procedures? ๐ An online training course can help you learn important concepts related to clinical research, Good Clinical Practice (GCP), clinical trial documentation, and the responsibilities of clinical research professionals.
Whether you are a life sciences graduate, pharmacy student, or aspiring Clinical Research Coordinator (CRC), consider exploring relevant online courses to improve your knowledge and prepare for future career opportunities.
๐ Explore Clinical Research Courses on Udemy
Discover online learning opportunities to develop your clinical research knowledge and professional skills.
Note: Completing an online course does not guarantee employment or replace the practical experience required for this vacancy.
Interested candidates can send their updated resumes to hr@mecrsindia.com, subject to confirmation that the recruitment is active.
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Good luck with your job search! ๐ฌ๐ผ
Disclaimer: JobsOnTheWay shares recruitment information to help job seekers discover employment opportunities. The details in this post are based on the information supplied for this vacancy and have not been independently verified. The employer controls the recruitment process, eligibility requirements, and final hiring decisions. Candidates should verify the information before sharing personal documents or making employment-related decisions.