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Clive
#496919 Sat, 05 Apr 08 10:24 PM
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Hi,
Please read the earlier posts in this thread and you'll find some examples.
Clive
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Joined on
Thu, Oct 28 2004
Canada
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El tango argentino es un pensamiento triste que se puede bailar (The tango argentino is a sad thought which can be danced) Enrique Santos Discépolo
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Anonymous
#497014 Sun, 06 Apr 08 06:07 AM
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Hi, Work experience certificate model can't be provided. This will lead to fraud. Best Regards
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Clive
#497020 Sun, 06 Apr 08 06:20 AM
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Hi,
That seems to me like a surprising opinion.
Do you also feel that providing formats and examples of resumes can lead to fraud?
Best wishes, Clive
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Anonymous
#504115 Wed, 23 Apr 08 06:08 AM
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I also need to lerned to right a work experience certificate formate
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Clive
#504244 Wed, 23 Apr 08 12:25 PM
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Hi,
Please read the earlier posts in this thread and you'll find some examples.
Clive
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Anonymous
#504763 Thu, 24 Apr 08 12:06 PM
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even i need it...riya..if u hv recievd ..plz post it
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Anonymous
#507715 Wed, 30 Apr 08 03:14 PM
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Anonymous
#511619 Fri, 09 May 08 01:07 PM
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Thank you very much. u r s truely ShreeVani.R
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Anonymous
#513049 Tue, 13 May 08 07:58 AM
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CERTIFICATE OF EXPERIENCE EMPLOYMENT DETAILS: Name of Employee: Suraj P Anand
Contract Management: iGATE Clinical Research International, 101/102 Alpha, Hiranandini Gardens, Powai, Mumbai 400076 Experience Obtained While Deployed at: Biometrics, Development Operations (Pfizer Global R&D) - India, 5, Patel Estate, Off S.V. Road Jogeshwari (W), Mumbai 400-102 Position/Title of Applicant: Biostatistician Period of Employment (Full Time): From: July 15, 2002 To: July 14, 2004 Name and Position of Supervisor: Dr Sundar Ramamoorthy, Manager, Biostatistics and Programming, DevOps (PGRD)-India Organizational Head of Site of Deployment: Dr Chitra Lele, Sr. Director, DevOps (PGRD)-India JOB SPECIFICATIONS: (Minimum educational requirement, special skills & knowledge and any other requirements needed for the satisfactory performance of the job) 1. Qualification- M.Sc or higher degree in Statistics/Biostatistics- 1 year experience in Applied Statistics/Biostatistics 2. Special Skill & Knowledge- Statistics/Biostatistics- Programming- Use of Statistical software, especially SAS- Clinical Research- Good Clinical Practices 3. Key Competencies- Analytical thinking- Concern for Quality- Customer Service- Initiative - Planning & Prioritizing- Team Work and Co-operation JOB ROLE AND KEY ACCOUNTABILITIES: 1. Strategic/Policy- Maintain quality and timeliness of assigned project work- Provide statistical input to study design and protocol- Review and provide comments on the Case Report Form and protocol 2. Operational- Write Statistical Analysis Plans and do the analysis and reporting for global clinical trials (Phase I, II and III) conducted by Pfizer Global Research and Development- Write SAS programs to do the analysis and reporting- Analyze the data and produce safety and efficacy tables for study reports- Write a statistical report based on the results
ACTIVITIES:
| Work experience at Pfizer (July 2002 – July 2004) |
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Study/ Therapeutic Area/ Program |
Activity Description |
| Phase I - Early Development (10 Protocols) Central Nervous System Chronic Obstructive Pulmonary Disease Absorption Distribution Metabolism Excretion Cardiovascular Bioavailability/ Bioequivalence |
Statistical Analysis Plan Statistical Report Quality Check for Safety and Efficacy Tables |
| Phase II/ Phase III (7 Protocols) Infectious Diseases (Global Malaria Program with 5 Protocols) Cardiovascular Chronic Obstructive Pulmonary Disease |
Inputs to Study Design Sample Size and Power Calculation Review of Protocol, Case Report Form, andClinical Study Report Interim Analysis Plan Statistical Analysis Plan Exploratory Analysis for Interim and Final analysis Quality Check for Safety and Efficacy Tables | PROFESSIONAL TRAINING AND DEVELOPMENT: 1. Completed web based training for the Pfizer Standard Operating Procedures regarding development, review, and approval of clinical protocol synopsis, full protocols, and protocol amendments as well as the conduct of protocol feasibility (2004)2. Completed web based training for the Pfizer Standard Operating Procedures regarding development, review, approval, amendment and implementation of Statistical Analysis Plans (2004)3. Completed web based training for the Pfizer Standard Operating Procedures regarding spontaneous reports of adverse events and safety reporting responsibilities (2004)4. Participated in the Corporate Pharmaceutical Regulatory Monitoring (CPRM) audit as a member of the Clinical Statistics team for Biometrics, Development Operations-India (2004)5. Attended the Good Clinical Practice (GCP) workshop conducted by Academy for Clinical Excellence (ACE) - India (2003)6. Attended the Malaria Investigator’s Meeting organized by Clinical-Operations (Pfizer) - India (2003)7. Attended workshop on ‘Quality’ organized by Development Operations (Pfizer) - India (2002)
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