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Full Time Job Vacancies in Akola

  • Fresher
  • 3.8 Lac/Yr
  • Akola
Copy-Paste Data Accuracy Data Entry Audit Data Entry Automation Data Entry Forms Data Entry Software Data Entry Speed Data Entry Validation Data Formatting Data Entry Accuracy Data Verification Data Quality Control Google Sheets
We are seeking a Data Entry Specialist to join our team in a part-time, work-from-home role. This position is ideal for freshers who have completed their 10th grade education and are looking to gain hands-on experience in data management.**Key Responsibilities:**- **Data Input:** Enter various types of data into company databases accurately and efficiently. This involves following specified formats and guidelines to maintain data integrity.- **Data Verification:** Review and confirm the accuracy of data entered into systems. Regular checks help identify any errors and ensure reliable data records.- **Data Maintenance:** Organize and update existing data as needed. Keeping records current is essential for effective data retrieval and reporting.- **Collaboration:** Work closely with team members and supervisors to understand data requirements and ensure tasks are completed on time.- **Reporting Issues:** Communicate any challenges or discrepancies encountered during data entry. This helps in addressing issues promptly and maintaining data quality.**Required Skills and Expectations:**Candidates should have good typing speed and accuracy to perform data entry tasks effectively. Attention to detail is crucial for spotting errors and ensuring correctness. Basic knowledge of computer applications, such as Microsoft Excel and Word, is preferred. Freshers should be willing to learn and adapt to new systems and procedures. Strong organizational skills and the ability to manage time effectively are necessary for this role, especially while working from home. Candidates must also have a reliable internet connection and a suitable workspace for productivity.
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Clinical Research Medical Coder Clinical Coordinator
Key Responsibilities:1. Trial Architecture:> Contribute to the development of dynamic trial plans and protocols in tandem with the clinical operations team.> Collaborate on the strategic selection and qualification of investigative sites.2. Site Symphony:> Conduct harmonious site initiation, monitoring, and close-out visits to ensure seamless protocol execution and pristine data collection.> Cultivate collaborative relationships with investigative site teams, providing support and guidance.3. Regulatory Mastery:> Ensure meticulous adherence to regulatory standards, guidelines, and the principles of Good Clinical Practice (GCP).> Spearhead the preparation and submission of regulatory documents to ethics committees and regulatory authorities.4. Data Choreography:> Direct the orchestration of data collection, ensuring the accuracy and completeness of clinical trial data.> Collaborate with data management teams to resolve data discrepancies and maintain a symphony of data quality.5. Risk Ballet:> Proactively identify potential risks to trial success and choreograph mitigation strategies in collaboration with project teams.6. Communication Sonata:> Cultivate clear and resonant communication channels with internal and external stakeholders.> Compose eloquent and timely study progress reports, fostering transparency and accountability.Qualifications:Bachelor's or advanced degree in a relevant field (Life Sciences, Nursing, etc.).Demonstrated experience as a Clinical Research Associate, preferably in the pharmaceutical or biotechnology domain.Profound knowledge of clinical trial processes, regulatory requirements, and GCP.Exceptional interpersonal and communication finesse
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