Walk-in Statistical Programmer & Biostatistician

Reporting Timing - 9 AM
  
Closing time : 11:00 AM
Contact Person - Marium Ansari/ Anita Thakur/ Richard Francis 
Drive Location - Bangalore & Mumbai
Venue - 


Bangalore:
IQVIA (Aura office), 
Opposite to new Horizon college, Marathalli Bangalore


Mumbai:-
IQVIA
Natraj By Rustomjee,  6th Floor, Near Western Express Highway Metro Station,  Andheri East, Mumbai - 400069



Skill Set - Statistical Programmer & Biostatistician
Relevant Work Experience - 2 to 10 Years
Work Location - Mumbai/ Bangalore

Note -
Clinical Domain Experience Mandatory
Candidates who have attended interview with IQVIA (QuintilesIMS) for the Same profile (Bio statistics team) in the past 6 months will not considered.

Job Description

1. Clinical domain Knowledge & Base SAS2
2. Good communication Skills
3. Exp in SAS Macros.
4. Creating Tables, Listing & Figures.
5. SDTM, ADAM + TLF Good exposure (Exp at least 1.5 yrs in live project)
6. Sample Size Calculation, Randomization, Mock Shell Creation etc.
7. Clinical Domain only.

Clinical SAS Programmers / Walkin

Novartis Healthcare is hiring ...!

Job location : Hyderabad.

Golden opportunity to meet our Programming directors and to visit our worldclass facility in hyderabad : 
Date : 21 APR 2017 @ 9:00 AM (Friday)
  
Venue details: 

Novartis Healthcare Pvt. Ltd.
Novartis Knowledge City, Salarpuria Sattva,
Near InOrbit Mall, Hitech City
Hyderabad.

Applications and queries can be sent to : Naresh_kumar.gunda@Novartis.com or call me on 040:67581684

Positions Vacant: 20
- Statistical Programmers : 3 - 5 Yrs.
- Senior or a Lead SAS Programmer - 5 - 9 Yrs.
- Principal or Sr.Principal Programmers - 9+ yrs.

Job Description:
- Locally coordinate and take responsibility for trial level programming activities (analysis datasets, pooled datasets, listings, tables and figures) of individual Phase I-IV clinical trials to support program programmers and statistician in project level activities.
- Be responsible for statistical tasks on assigned clinical trials e.g. RAP.
- Maintain efficient interfaces with internal and external customers with support of ONC Biometrics management and the Program Programmer/Statistician.
- Make certain that documents and specifications are consistent and comply with company standards by providing input into CRF and data structures tables, listings and figures for phase I-IV clinical trials and submission activities.
- Program and deliver, according to specifications, analysis datasets, pooled datasets, listings, tables, and figures for phase I-IV clinical trials and for pooled analysis with high quality and within milestones.
- In consultation with the statistician, develop specifications for analysis datasets, pooled datasets, and listings
- Maintain records for all assigned projects and archiving of trial / project analysis and associated documentation.
- Provide input on process improvement initiatives and participate in non-clinical project activities with support from GH


Please share this email in your network, to help someone waiting for an opportunity to work with Novartis Health care.

Note :Only the applicants/ direct walk-ins with 3yrs and above of relevant experience in Clinical SAS would be considered for the interview

You are requested to carry the following documents:

- 2 copies of Resume

- Recent  3 Months Salary slips

- Detailed salary breakup (Offer letter / Appraisal letter)

Multiple Job Opportunities for Clinical SAS Programmers & Bio statistician

Job Location: Mumbai/ Bangalore

Work Experience: 2 to 9 Years

Skills / Knowledge: Clinical SAS Programming, SDTM , ADAMs , TLF , Macros, Safety & Efficacy Datasets , Phase I to IV Clinical Trials.

Role: SAS Programmer / Bio statistician

We have requirement for various positions in Statistical Programming and Biostatistics. Please share your updated profile mentioning your roles and responsibilities.

Job Description:
1. Clinical domain Knowledge & Base SAS2
2. Good communication Skills
3. Exp in SAS Macros.
4. Creating Tables, Listing & Figures.
5. ADAM + TLF Good exposure (Exp at least 1.5 yrs in live project)
6. Clinical Domain only.

REQUIRED KNOWLEDGE, SKILLS AND ABILITIES
Good knowledge of applicable clinical research regulatory requirements; i.e., ICH GCP and relevant local laws,
regulations and guidelines 
Strong written and verbal communication skills including good command of English language 
Results and detail-oriented approach to work delivery and output
Good problem solving skills 
Good planning, time management and prioritization skills 
Attention to detail and accuracy in work 
Good software and computer skills, including MS Office applications including but not limited to Microsoft Word, Excel
and PowerPoint 
Ability to establish and maintain effective working relationships with coworkers, managers and clients. 
Proven ability to work on multiple projects balancing competing priorities 
Ability to coach/ mentor junior colleagues

MINIMUM REQUIRED EDUCATION AND EXPERIENCE

Bachelor's degree in life sciences or related field and min 2 years relevant experience; or equivalent combination of education, training and experience


Kindly carry a copy of your resume,1 passport size photo and a copy of ID Proof(Pan Card).

Note: Experienced candidates only apply.

Walk-in on 18th March

Company: Quintiles

Venue Details:-
Manpowergroup Services India Pvt. Ltd.
1-8-384 & 385,Office No#202,2nd Floor,
Gowra Grand,S.P Road,
Begumpet,Secunderabad-500 003
Telangana, India 
Landmark : Opp to Bowl of China Restaurant , Beside Mody Ford Showroom

Novartis hiring for Clinical SAS Programmers

- Statistical Programmers : 3 - 5 Yrs.
- Senior or a Lead SAS Programmer - 5 - 9 Yrs.
- Principal or Sr.Principal Programmers - 9+ yrs.

Job Description:
- Locally coordinate and take responsibility for trial level programming activities (analysis datasets, pooled datasets, listings, tables and figures) of individual Phase I-IV clinical trials to support program programmers and statistician in project level activities.
- Be responsible for statistical tasks on assigned clinical trials e.g. RAP.
- Maintain efficient interfaces with internal and external customers with support of ONC Biometrics management and the Program Programmer/Statistician.
- Make certain that documents and specifications are consistent and comply with company standards by providing input into CRF and data structures tables, listings and figures for phase I-IV clinical trials and submission activities.
- Program and deliver, according to specifications, analysis datasets, pooled datasets, listings, tables, and figures for phase I-IV clinical trials and for pooled analysis with high quality and within milestones.
- In consultation with the statistician, develop specifications for analysis datasets, pooled datasets, and listings
- Maintain records for all assigned projects and archiving of trial / project analysis and associated documentation.
- Provide input on process improvement initiatives and participate in non-clinical project activities with support from GH

Please share this to  your network, to help someone waiting for an opportunity to work with Novartis Health care.


You are requested to carry the following documents:
- 2 copies of Resume
- Recent  3 Months Salary slips
- Detailed salary breakup (Offer letter / Appraisal letter)


Job location : Hyderabad.

Note :Only the applicants/ direct walk-ins with 3yrs and above of relevant experience in Clinical SAS would be considered for the interview

Walk-in -Date : 18 FEB 2017 @ 9:00 AM (Saturday)

Venue: 
Novotel Bengaluru Techpark, 
Opposite RMZ Ecospace Business Park, 
Marathahalli - Sarjapur Outer Ring Road, 
Bengaluru 560103, Karnataka, India
T: +91 (80) 66700600 I M: +91 9538897361 .

Multiple Job Opportunities for Clinical SAS Programmers & Bio statisticians

Skills / Knowledge: Clinical SAS Programming, SDTM , ADAMs , TLF , Macros, Safety & Efficacy Datasets , Phase I to IV Clinical Trials.

Role: SAS Programmer / Bio statistician

Key Pointers:

1. TLF / SDTM Programming.
2. Creating Tables, Listing & Figures.
3. CRF annotation in accordance with CDISC
4. Development and Validation of SDTM datasets using SAS in accordance with the aCRF, Standard Operating Procedures(SOPs) and departmental guidelines
5. Create Define.XML 
6. Use OPENCDISC to check data inconsistencies
7. Proficiency in understanding of Study Protocols, CRT specification, aCRF, eCRF and SAP
8. Technical skill: SDTM Trained and Experienced candidates

REQUIRED KNOWLEDGE, SKILLS AND ABILITIES

• Good knowledge of applicable clinical research regulatory requirements; i.e., ICH GCP and relevant local laws,
• regulations and guidelines 
• Strong written and verbal communication skills including good command of English language 
• Results and detail-oriented approach to work delivery and output
• Good problem solving skills 
• Good planning, time management and prioritization skills 
• Attention to detail and accuracy in work 
• Good software and computer skills, including MS Office applications including but not limited to Microsoft Word, Excel
• and PowerPoint 
• Ability to establish and maintain effective working relationships with coworkers, managers and clients. 
• Proven ability to work on multiple projects balancing competing priorities 
• Ability to coach/ mentor junior colleagues

MINIMUM REQUIRED EDUCATION AND EXPERIENCE 

Bachelor's degree in life sciences or related field and min 2 years relevant experience; or equivalent combination of education, training and experience


Kindly carry a copy of your resume,1 passport size photo and a copy of ID Proof(Pan Card).


Walkin on 18th feb '17 from 9AM
Job Location: THANE (MUMBAI)

Work Experience: 2 to 9 Years

Note: Experienced candidates only apply. 

Venue Details:-
Quintiles Research (India) Pvt. Ltd. 
Natraj by Rustomjee 
 6th Floor, 602A, 
 194, MV Road, 
 Near Western Express Highway Metro Station 
 Andheri East 
 Mumbai 400 069