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1.0 - 5.0 years
0 Lacs
pune, maharashtra
On-site
As a Sr. Technical Support Engineer at our company, your role will involve providing technical leadership, troubleshooting critical infrastructure, and ensuring smooth server operations. We are looking for someone with 1-2 years of experience in a hosting environment, particularly skilled in server management, cloud platforms, and networking tools. If you possess excellent problem-solving abilities, effective communication skills, and technical mentoring capabilities, we welcome you to apply for this challenging and rewarding position. **Roles and Responsibilities:** - **Technical Leadership:** - Provide mentorship and guidance to teammates through coaching. - Lead technical operations in mi...
Posted 3 weeks ago
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 2 months ago
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 3 months ago
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 5 months ago
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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