Clinical Research Coordinator Job: Are you an experienced clinical research professional looking for an exciting career opportunity in oncology research? Somaya Research and Health Services LLP is currently hiring a Clinical Research Coordinator (CRC) for its clinical research facility located in Patel Nagar, Dehradun, Uttarakhand. This is an excellent opportunity for professionals with experience in Oncology Clinical Trials to contribute to high-quality clinical research while working in a dynamic and collaborative environment. Pharmaacademias.com
If you have a strong understanding of clinical trial coordination, regulatory compliance, patient management, and Good Clinical Practice (GCP), we encourage you to apply immediately.
Clinical Research Coordinator Job Details
| Particular | Information |
| Job Title | Clinical Research Coordinator (CRC) |
| Company | Somaya Research and Health Services LLP |
| Location | Patel Nagar, Dehradun, Uttarakhand |
| Job Type | Full-Time |
| Industry | Clinical Research / Healthcare / Pharmaceuticals |
| Department | Clinical Research |
| Experience Required | Experience in Oncology Clinical Trials (Mandatory) |
| Qualification | B.Pharm, M.Pharm, or equivalent qualification |
| Joining | Immediate |
| Salary | As per interview |
About the Company
Somaya Research and Health Services LLP is dedicated to delivering high-quality clinical research services while maintaining the highest standards of ethics, patient safety, and scientific integrity. The organization works closely with investigators, healthcare professionals, sponsors, and regulatory authorities to conduct clinical trials that contribute to the development of innovative and effective healthcare solutions.
The company values professionalism, teamwork, continuous learning, and adherence to international clinical research standards, making it an ideal workplace for professionals who are passionate about advancing medical science.
Clinical Research Coordinator job Position Overview
The Clinical Research Coordinator (CRC) plays a vital role in the successful execution of clinical trials. The selected candidate will coordinate all aspects of assigned clinical studies, ensuring that each trial is conducted according to approved protocols, regulatory guidelines, Good Clinical Practice (ICH-GCP), and applicable ethical standards.
The role requires excellent communication skills, strong documentation practices, effective coordination with investigators and sponsors, and the ability to manage multiple clinical trial activities simultaneously.
Key Responsibilities of Clinical Research Coordinator job
The selected candidate will be responsible for:
- Coordinating daily clinical trial activities from study initiation to study close-out.
- Assisting Principal Investigators in the execution of oncology clinical studies.
- Screening, recruiting, and scheduling eligible study participants.
- Obtaining and maintaining complete informed consent documentation.
- Coordinating participant visits according to study protocols.
- Maintaining source documents and Case Report Forms (CRFs).
- Ensuring accurate and timely data entry into Electronic Data Capture (EDC) systems.
- Maintaining Investigator Site Files (ISF) and Trial Master File (TMF) documentation.
- Managing essential regulatory documents required for clinical trials.
- Coordinating with sponsors, Clinical Research Associates (CRAs), ethics committees, laboratories, and hospital departments.
- Preparing study documentation for monitoring visits, audits, and regulatory inspections.
- Reporting Serious Adverse Events (SAEs) and adverse events according to protocol requirements.
- Ensuring participant safety, confidentiality, and protocol compliance throughout the study.
- Tracking study milestones and ensuring timely completion of trial activities.
- Maintaining drug accountability records and investigational product documentation where applicable.
- Assisting in study start-up, site initiation, monitoring, and close-out activities.
- Ensuring compliance with ICH-GCP guidelines, SOPs, and regulatory requirements.
Eligibility Criteria
Applicants should possess the following qualifications:
- Bachelor’s degree in Pharmacy (B.Pharm)
- Master’s degree in Pharmacy (M.Pharm)
- Or another relevant qualification in life sciences, clinical research, or allied healthcare disciplines.
Mandatory Requirements
Candidates must have experience in Oncology Clinical Trials.
Applicants without oncology clinical trial experience may not be considered for this position.
Preferred Skills
Successful candidates should possess:
- Strong knowledge of ICH-GCP guidelines.
- Good understanding of clinical trial protocols.
- Knowledge of regulatory documentation.
- Experience with CRFs and EDC systems.
- Familiarity with ethics committee submission processes.
- Excellent organizational and time management skills.
- Strong interpersonal and communication abilities.
- Ability to work independently and collaboratively.
- High attention to detail and accuracy.
- Professional attitude and commitment to patient safety.
- Problem-solving and decision-making abilities.
Why Join Somaya Research and Health Services LLP?
Joining Somaya Research and Health Services LLP offers an opportunity to become part of an organization committed to advancing clinical research through scientific excellence and ethical practices. Employees gain valuable exposure to oncology clinical trials while working alongside experienced investigators and research professionals.
Benefits include:
- Opportunity to work on cutting-edge oncology clinical research.
- Professional and supportive work environment.
- Exposure to international clinical research standards.
- Opportunities for continuous learning and professional development.
- Experience working with multidisciplinary healthcare teams.
- Career growth within the clinical research industry.
- Meaningful contribution to improving patient care and advancing medical science.
Who Should Apply?
This opportunity is ideal for:
- Experienced Clinical Research Coordinators.
- Pharmacy graduates with oncology clinical trial experience.
- Professionals seeking career growth in clinical research.
- Candidates interested in working in oncology research.
- Individuals who can join immediately.
Salary
Compensation will be offered as per interview and will depend on the candidate’s qualifications, relevant experience, technical knowledge, and overall performance during the selection process.
Application Process
Interested and eligible candidates are invited to send their updated resume to the email address below:
Email: [email protected]
Please mention “Application for Clinical Research Coordinator (CRC)” in the subject line of your email to facilitate the recruitment process.
If you meet the eligibility criteria and have hands-on experience in Oncology Clinical Trials, don’t miss this excellent opportunity to build your career with Somaya Research and Health Services LLP.
Immediate joiners will be given preference.
Submit your application today and take the next step toward a rewarding career in clinical research.
Frequently Asked Questions (FAQs)
1. What is the job title for this vacancy?
The available position is Clinical Research Coordinator (CRC) at Somaya Research and Health Services LLP.
2. Where is the job located?
The position is based in Patel Nagar, Dehradun, Uttarakhand, India.
3. What qualifications are required for this role?
Candidates should possess B.Pharm, M.Pharm, or an equivalent qualification in a relevant field.
4. Is experience mandatory?
Yes. Experience in Oncology Clinical Trials is mandatory for this position.
5. Can freshers apply for this job?
No. This position is intended for candidates with relevant experience in oncology clinical trials.
6. What type of employment is being offered?
This is a full-time Clinical Research Coordinator (CRC) position.
7. What will be the key responsibilities of the Clinical Research Coordinator?
The selected candidate will coordinate clinical trials, manage study documentation, ensure protocol compliance, schedule patient visits, maintain regulatory records, support monitoring visits, and work closely with investigators, sponsors, and ethics committees.
8. Is knowledge of ICH-GCP guidelines required?
Yes. A good understanding of ICH-GCP (International Council for Harmonisation – Good Clinical Practice) guidelines and clinical research regulations is highly desirable.
9. What therapeutic area is involved in this position?
This position specifically involves Oncology Clinical Trials.
10. What is the expected joining date?
The company is looking for immediate joiners.
11. What salary is being offered?
The salary will be as per interview, depending on qualifications, experience, and overall performance during the selection process.
12. How can I apply for this position?
Interested candidates can send their updated resume to:
Email: [email protected]
13. What should I mention in the email subject line?
Applicants are encouraged to mention “Application for Clinical Research Coordinator (CRC)” in the email subject line.
14. Are candidates from other states eligible to apply?
Yes. Candidates from any state in India may apply, provided they meet the eligibility criteria and are willing to work in Dehradun, Uttarakhand.
15. What skills are preferred for this role?
Preferred skills include:
- Knowledge of clinical trial coordination
- Oncology clinical trial experience
- ICH-GCP compliance
- Regulatory documentation
- Good communication skills
- Time management
- Patient coordination
- Teamwork
- Attention to detail
16. Will there be opportunities for career growth?
Yes. This position offers valuable experience in oncology clinical research and provides opportunities to develop expertise in clinical trial management and regulatory compliance.
17. Is relocation required?
Yes. Candidates should be willing to work from the company’s location in Patel Nagar, Dehradun, Uttarakhand.
18. Who should apply for this position?
This opportunity is ideal for experienced Clinical Research Coordinators and pharmacy professionals who have worked on oncology clinical trials and are looking to advance their careers in clinical research.
19. Is this opportunity suitable for B.Pharm graduates?
Yes. B.Pharm graduates with the required oncology clinical trial experience are eligible to apply.
20. Why should I apply for this job?
This role offers the opportunity to work on oncology clinical trials, collaborate with experienced research professionals, gain exposure to regulatory processes, and contribute to advancing patient care through clinical research.
