Clinical Research Coordinator BIOSPECIMEN SOLUTIONS PRIVATE LIMITED

2.0 - 6.0 years

0 Lacs

karnataka

On-site

You will be responsible for overseeing the day-to-day operations of clinical research studies at Biospecimen Solutions Pvt Ltd. This includes tasks such as obtaining informed consent, adhering to protocols, managing research activities, and ensuring compliance with clinical trial regulations. Key Responsibilities: - Coordinate the day-to-day operations of clinical research studies - Obtain informed consent from study participants - Follow protocols outlined for each research study - Manage various research activities as required - Ensure compliance with all clinical trial regulations Qualifications Required: - Possess skills in informed consent and protocol management - Previous experience i...

Posted 1 month ago

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Clinical Research Coordinator Seema Hospital and Eva Fertility Clinic & IVF Center

2.0 - 6.0 years

0 Lacs

azamgarh, uttar pradesh

On-site

Role Overview: As a Clinical Research Coordinator, your primary responsibility will be to recruit and enroll study participants for research projects. You will input clinical research data into electronic data systems, coordinate patient visits and procedures, and act as a resource for study participants by addressing their inquiries and explaining related procedures. Ensuring compliance with all local and federal laws and regulations at the study site will be part of your duties. Additionally, you will create comprehensive documentation of study protocols and update them as needed. Coordinating with study sites, sponsors, ethics committees, and Principal Investigators for the smooth conduct...

Posted 1 month ago

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Clinical Research Coordinator Q-Max Clinical Research

2.0 - 6.0 years

0 Lacs

gujarat

On-site

You will be joining Q-Max Clinical Research Services as a Clinical Research Coordinator at their Nadiad location. Your primary responsibilities will include managing tasks related to informed consent, protocol management, research coordination, and supporting clinical trials. To excel in this role, you should possess skills in informed consent and protocol management, along with previous experience in clinical research and coordinating clinical trials. Attention to detail and strong organizational skills are crucial for success in this position. Additionally, effective communication, excellent interpersonal skills, and the ability to work collaboratively in a team environment are essential. ...

Posted 3 months ago

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Executive Assistant Suntuity Renewable Energy India

2.0 - 6.0 years

3 - 6 Lacs

mumbai

Work from Office

Key Responsibilities Executive Support & Coordination Manage daily calendar, appointments, and meeting schedules across multiple time zones. Coordinate high-level meetings with senior government officials, global stakeholders, and industry leaders. Draft, review, and manage official correspondence, briefings, memos, and policy papers. Handle sensitive and confidential information with discretion. Prepare meeting materials, talking points, and presentations for key engagements. Stakeholder Engagement Facilitate communication with ministries, embassies, and regulatory bodies. Liaise with internal and external stakeholders on behalf of the advisor. Maintain an updated network map of government ...

Posted Date not available

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