MSc Biotechnology Jobs in Clinical Research at Promed Hospital
Company: Promed Hospital
Job Title: Clinical Research Coordinator
Location: Thiruvanmiyur/ Chennai
Type: Full Time
Experience Required: Min 2 years
Salary Range: Based on current CTC (hike 5-10%)
Education Required: BSc or PG degree in Biotechnology or equivalent with minimum 2 years’ experience in a NABH 100 bedded hospital
Joining Timeline: Immediate to 30 days
Interview Mode: F2F
About Company:
Promed is a multispecialty hospital with a focus on delivering trustworthy and ethical medical care. We pride ourselves in providing well trained and experienced physicians in combination with courteous staff and state of the art infrastructure. Promed is one of its kind preventive healthcare hospital, wellness and rehab center with multispecialty diagnostic facilities.
JOB RESPONSIBILITIES OF CLINICAL RESEARCH
Qualification: BE or PG degree in Biotechnology or equivalent with minimum 2 years’ experience in a NABH 100 bedded hospital with actual exposure on various phases of Clinical trials and follow up.
Reporting to: Director
RESPONSIBILITIES
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Trial Protocols: Manage clinical trials from feasibility assessment to study close-out, ensuring adherence to protocols and regulations with specifics to Cardiology department.
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Patient Recruitment: Oversee subject (Patient) enrollment, including screening, recruiting, obtaining informed consent, and follow-up maintaining accuracy and confidentiality.
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Regulatory compliance:
Monitor clinical trials for regulatory compliance, ensuring adherence to site requirements. -
Follow TAT: Ensure timely completion of study tasks and meet project timelines. Liasion role: Collaborate with investigators, sponsors, and cross-functional teams to drive study success.
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Accurate Reporting & data submission: Identify discrepancies in data and processes, resolving issues promptly. Prepare and maintained essential regulatory documents, including IRB submissions and safety reports. Manage Serious Adverse Events (SAEs) with accurate reporting and resolution.
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Data capture Screen, recruit: Obtain consented participants, maintain comprehensive study records and data in Backbone – Electronic Data Capture (EDC) system besides accurate and timely documentation including case report forms and trial protocols.
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Quality Assurance: Monitor and audit research processes to ensure adherence to trial protocols and quality standards.
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Training & Support: Educate and train clinical staff on trial protocols, procedures, and data collection methods.
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Report Preparation: Compile and present interim and final reports for ongoing studies to the Director and other stakeholders.
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Grant Applications: Assist in preparing research grant proposals and securing funding for clinical studies.
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Follow-Up Coordination: Track patient follow-ups as per trial requirements and ensure continuity of care.
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Innovation & Updates: Stay updated on cardiology-related research advancements and propose innovative ideas for future studies.
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