Here are a bunch of Pharma / Biotech requirements with my client. Please email only the best suitable resume / updated according to the requirement at KSR@delightconsulting.com with rate and contact details and I will call you. Thanks
1) Data Management SAS Programmer
LOCATION: Boston, MA
RATE: Open
START DATE: ASAP
DURATION: 6+ month contract
Job Description:
As a Contract Data Management SAS Programmer, you will joining a Data Management team and providing SAS programming support including data quality checks, extracts, and standardizations.
Responsibilities:
Designing programs to provide standard and ad-hoc data quality checks across all studies.
Extract data from Medidata Rave (raw SAS datasets) and convert them into project standards.
Provide guidance to Data Integration Specialist to facilitate the SAS programming management related to the import/export of data
databases.
Qualifications:
BS degree in Computer or Life Sciences
3 or more years of SAS programming working for a pharmaceutical or biotech company.
Experience with Medidata Rave.
Prior experience with Oncology clinical trials.
2) MedDRA Coding Consultant
LOCATION: Boston, MA
RATE: Open
START DATE: ASAP
DURATION: 6+ month contract
Job Description:
As a MedDRA Coding Consultant you will be joining a centralized medical coding team that is responsible for the conduct of all coding activities with a pharmaceutical company.
Responsibilities (will include, but not limited to):
- Coding of all drug safety and pharmacovigilance cases (post-marketing and clinical trial serious AEs)
-Ensure quality, consistency, and overall excellence of all medical coding activities through ongoing QC and peer review
-Oversight of all coding performed by external vendors
Qualifications:
- You will have prior work experience within a pharma company.
Must have a PharmD or RN degree, with current licensure preferred
- Possess extensive knowledge of MedDRA dictionary, with 5+ years of clinical coding experience.
3) Manager of Clinical Data Standards
LOCATION: Boston, MA
RATE: Open
START DATE: ASAP
DURATION: 6+ month contract
Job Description:
As the Clinical Data Standards Manager you will be implementing clinical data standards specific to database build and analysis and reporting of outsourced studies, and ensuring data quality throughout the clinical trial lifecycle.
Responsibilities:
-Establishing and implementing study standards with outsourced studies
-Performing in the capacity of project manager for the deliverables supporting the reporting requirements under the IND application
-Monitoring and escalating any study specific challenges and/or change requests
Qualifications:
-BS or MS degree in health related field. 3-5 years experience in clinical data management, data management programming, or clinical operations, with a focus on data quality.
-Solid project management skills, as well as vendor management.
-Solid understanding of implementation of standards , including CDISC.
-Exceptional communication skills, written and verbal.
4) Metadata Analyst
LOCATION: Boston, MA
Rate: Open
START DATE: ASAP
DURATION: 6+ month contract
Job Description:
As a contract Metadata Analyst you will be part of a metadata operations group responsible in managing the global standard metadata that's stored within the tables of a clinical integrated data repository.
Responsibilities:
Managing the global standard metadata that resides in the clinical integrated data repository (CIDR).
Direct data assessments of the source data for loading into CIDR.
Review data for consistency and quality.
Qualifications:
You will have 3 to 5 years of experience working in a pharmaceutical company.
Have a BS degree, preferable in a field related to clinical data management systems
Experience with a CRO is strongly preferred.
Have knowledge of MedDRA and Who medical coding dictionaries.
5) Biostatistician
Cambridge MA
RATE: Open
START DATE: 7/30/12
DURATION: 6+ month contract
Job Description:
As a contract Biostatistician, you will be providing development and filing statistical support for ongoing Phase II and III oncology clinical trials development and submission filing.
Responsibilities:
As a Biostatistician you will be responsible for:
-analysis planning
-ISS/ISE statistical plan implementations
-TFL shell developments
-Ad hoc data analysis
Qualifications:
-MS or PhD degree in Statistics/Biostatistics
-Have 3-5 years pharmaceutical industry experience.
-Have SAS programming experience
-Knowledge of NDAs/BLAs/INDs/eCTD submissions
Please email only the best suitable resume / updated according to the requirement at KSR@delightconsulting.com with rate and contact details
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Regards
Santosh
Delight Consulting Services LLC.
2565 S. Rochester Road,
Suite# 107A,
Rochester, MI 48307.
Phone: 248-680-6684 ext 307
Fax: 248-498-6195
Email: ksr@delightconsulting.com
kakulasr.delightcs@gmail.com
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