DepartmentCPS JobsLocationHyderabad, Andhra Pradesh, India
Apply Here: http://jobs.parexel.com/in/hyderabad/cps/jobid4135371-senior-data-entry-associate-jobs
Job Description :
Join a team that is recognized not only for our life-changing work, but also for our expertise and breadth of experience Previously, PAREXEL has been named company of the year for the Pharmaceutical Industry in International Business Awards (SM) and ranked as a Best 5 outsourcing company for the Pharmaceutical Industry by The International Outsourcing Professionals.
PAREXEL Contract Personnel Services (CPS) specialises in placing experienced clinical research professionals with top pharmaceutical, biotechnology and medical device companies worldwide. CPS staff are employed on permanent contracts and our dedicated management has extensive experience in clinical research, so we understand the challenges you face as clinical research professionals and can provide you with the greatest opportunities to achieve your personal and professional goals.
Currently CPS is looking for a number of Data Entry Associates / Senior Data Entry Associates to join one of the largest most innovative companies in the pharmaceutical arena. This position will be office based in Hyderabad, India.
The Data Entry Associates will be responsible for maintaining the CTMS (IMPACT) reference data and supporting the clinical teams by updating information in CTMS for their clinical studies and ensuring data quality and completeness in the system.
Whilst on assignment, you will receive continued support from a dedicated Manager at PAREXEL. We are committed to supporting professional growth and rewarding excellence and we offer a full performance management and development process providing continuous monitoring and on-going review of staff performance standards in order to allow staff to reach their full potential. You will also benefit from access to our extensive technical and soft skills training, to help your career growth.
Key Accountabilities:
- Create and maintain all clinical studies (approximately 100 studies) in CTMS on daily basis. All updates should be completed within 5 days of receipt of data/reports.
- Follow up with the study team to ensure data completeness using IMPACT reports and resolve any queries in a timely manner within 5 days
- Data to create/maintain include:
• Addresses, telephone, fax and email contact information for investigators, IEC/IRBs and other site personnel for each study
• Company personnel for each study
• Study level milestones, protocol design information, recruitment plan, etc.
• Country level milestones, regulatory approval information, recruitment plan, etc.
• Site level milestones, recruitment information, etc.
- For studies where data loading is being handled, the Data Entry Associate will checks and follow up with the study teams if errors are found during the loading process.
- Provide support to end-users directly or by channelling requests to the sponsor
- Compliance check should be completed on monthly basis using the Quality Check reports and follow up with study teams for any missing and data quality issues
- Data cleaning, new data entry, or rectification needed in CTMS
Benefits
Our success is built on recruiting the best available talent and providing exemplary benefits in an effort to develop long-term relationships. As a CPS employee, the following benefits are available to you:
- Highly competitive salaries
- Expense reimbursement
- Paid holidays, vacation, and other time off
- Work-life balance policy
- Excellent Benefits (tailored by country) including pension, health care, dental care, life insurance, etc.
Qualifications :
- Relevant experience in maintenance of computer-based records. Previous experience in use of a clinical trial management system (CTMS) is preferred.
- Computer literate, especially in use and management of databases and spread sheet reports
- Basic understanding of the use of electronic systems in regulated environments is preferable
- Basic understanding of clinical development processes is preferable
- Good organisational skills
- Diligent and reliable
- Ability to recognise problems / potential problems and alert management and/or take action as appropriate
- Able to prioritise routine work
- Language requirements: good written and spoken English
applyJob Description :
Join a team that is recognized not only for our life-changing work, but also for our expertise and breadth of experience Previously, PAREXEL has been named company of the year for the Pharmaceutical Industry in International Business Awards (SM) and ranked as a Best 5 outsourcing company for the Pharmaceutical Industry by The International Outsourcing Professionals.
PAREXEL Contract Personnel Services (CPS) specialises in placing experienced clinical research professionals with top pharmaceutical, biotechnology and medical device companies worldwide. CPS staff are employed on permanent contracts and our dedicated management has extensive experience in clinical research, so we understand the challenges you face as clinical research professionals and can provide you with the greatest opportunities to achieve your personal and professional goals.
Currently CPS is looking for a number of Data Entry Associates / Senior Data Entry Associates to join one of the largest most innovative companies in the pharmaceutical arena. This position will be office based in Hyderabad, India.
The Data Entry Associates will be responsible for maintaining the CTMS (IMPACT) reference data and supporting the clinical teams by updating information in CTMS for their clinical studies and ensuring data quality and completeness in the system.
Whilst on assignment, you will receive continued support from a dedicated Manager at PAREXEL. We are committed to supporting professional growth and rewarding excellence and we offer a full performance management and development process providing continuous monitoring and on-going review of staff performance standards in order to allow staff to reach their full potential. You will also benefit from access to our extensive technical and soft skills training, to help your career growth.
Key Accountabilities:
- Create and maintain all clinical studies (approximately 100 studies) in CTMS on daily basis. All updates should be completed within 5 days of receipt of data/reports.
- Follow up with the study team to ensure data completeness using IMPACT reports and resolve any queries in a timely manner within 5 days
- Data to create/maintain include:
• Addresses, telephone, fax and email contact information for investigators, IEC/IRBs and other site personnel for each study
• Company personnel for each study
• Study level milestones, protocol design information, recruitment plan, etc.
• Country level milestones, regulatory approval information, recruitment plan, etc.
• Site level milestones, recruitment information, etc.
- For studies where data loading is being handled, the Data Entry Associate will checks and follow up with the study teams if errors are found during the loading process.
- Provide support to end-users directly or by channelling requests to the sponsor
- Compliance check should be completed on monthly basis using the Quality Check reports and follow up with study teams for any missing and data quality issues
- Data cleaning, new data entry, or rectification needed in CTMS
Benefits
Our success is built on recruiting the best available talent and providing exemplary benefits in an effort to develop long-term relationships. As a CPS employee, the following benefits are available to you:
- Highly competitive salaries
- Expense reimbursement
- Paid holidays, vacation, and other time off
- Work-life balance policy
- Excellent Benefits (tailored by country) including pension, health care, dental care, life insurance, etc.
Qualifications :
- Relevant experience in maintenance of computer-based records. Previous experience in use of a clinical trial management system (CTMS) is preferred.
- Computer literate, especially in use and management of databases and spread sheet reports
- Basic understanding of the use of electronic systems in regulated environments is preferable
- Basic understanding of clinical development processes is preferable
- Good organisational skills
- Diligent and reliable
- Ability to recognise problems / potential problems and alert management and/or take action as appropriate
- Able to prioritise routine work
- Language requirements: good written and spoken English
About CPS Jobs
By being hired into one of our CPS jobs at PAREXEL International, you’ll be a key member of the PAREXEL International team. Professionals in CPS careers come from a variety of backgrounds, bringing an assortment of knowledge and skills to every area of our business. Please click on your desired CPS job below to learn more about the exact qualifications.A job in CPS at PAREXEL International may be waiting for you!
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