Biotech Healthcare hiring Clinical Operations Specialist | Pharma Freshers | Apply Now
Looking for a Clinical Research Job and a Pharma Freshers Job opportunity in Ahmedabad? Biotech Healthcare is hiring Clinical Operations Specialists for freshers and candidates with up to 1 year of experience. This Clinical Research Job offers excellent exposure to clinical trials, regulatory submissions, ethics committee coordination, trial documentation, and clinical operations activities. Candidates with B.Pharm. and M.Pharm qualifications can apply for this exciting Pharma Freshers Job in the clinical affairs department.
- Role: Clinical Operations
- Job Location: Corporate Office, Ahmedabad
About the Company
Biotech Healthcare is a leading pharmaceutical and healthcare company focused on innovation, quality, and patient care. The company works across multiple healthcare segments and provides opportunities for fresh graduates to build careers in clinical research, clinical operations, regulatory affairs, and pharmaceutical sciences. Biotech Healthcare promotes diversity and equal opportunity while maintaining high ethical and professional standards.
Job Description
This role will support the coordination and execution of clinical trial activities, including regulatory and ethics committee submissions, site coordination, trial documentation, study material management, and compliance with applicable SOPs, local regulations, and ICH-GCP guidelines.
Key Responsibilities
- Support the ethics committee and regulatory submissions for clinical trials.
- Assist in clinical trial registration and study documentation activities.
- Coordinate with study sites for data collection and project documentation.
- Help manage clinical trial materials, investigational products, and study supplies.
- Maintain and track case report forms (CRFs) and trial records.
- Ensure compliance with SOPs, ICH-GCP guidelines, and regulatory requirements.
- Support site initiation, monitoring, and close-out visit activities.
- Coordinate with investigators, vendors, site staff, and internal teams for smooth trial execution.
- Assist in protocol amendments, site additions, and regulatory notifications.
- Maintain Trial Master File (TMF) and other clinical documentation accurately.
- Identify and report study-related issues on time.
- Perform additional clinical operations and coordination tasks as assigned.
Qualifications
Education
- B.Pharm/M.Pharm (Pharmacology or Pharmaceutics) or M.Sc. (Life Sciences or Clinical Research)
Experience
- Fresher to 1 year of relevant exposure in clinical research, clinical operations, CRO/site coordination, hospital-based clinical projects, or internship/training in clinical trials.
Skills
- Basic understanding of clinical trial processes, ethics committee documentation, regulatory submissions, CRFs, source documents, trial supplies, and data collection requirements.
Attributes
- Quick learner with attention to detail, ethical conduct, professional communication, willingness to travel for site visits when required, and ability to coordinate with investigators, sites, vendors, and internal teams.
Functional Skills
- Good communication and professional interaction skills.
- Strong attention to detail and accurate documentation handling.
- Quick learner with the ability to work under guidance.
- Good planning, coordination, and follow-up abilities.
- Problem-solving mindset with timely issue reporting skills.
- Team player with integrity, adaptability, and willingness to travel for site activities.
Behavioral Skills
- Strong written and verbal communication skills with professional etiquette.
- High attention to detail, documentation discipline, and commitment to accuracy and timelines.
- Ability to learn quickly, take guidance positively, and work effectively under supervision.
- Good planning, coordination, prioritization, and follow-up skills for handling multiple sites and project activities.
- Problem-solving mindset with the ability to identify issues early and escalate appropriately.
- Integrity, confidentiality, teamwork, adaptability, and willingness to travel for site activities when required.
