Kyiv, Kiev, Ukraine
$65/hr · Starting at $1,000
• Perform and coordinate all aspects of clinical monitoring and site management process in accordance with ICH, GCP, FDA Guidelines, local regulations and client SOPs • Obtain, review for appropriaten…
Rocky Hill, Connecticut, United States
$5/hr · Starting at $25
Cinical SAS Programmer with good understanding of Clinical Trial Life Cycle, Phases and CDISC Standards including SDTM, ADam and good experience in SAS/Base, SAS/Functions, SAS/Macros, SAS/ODS, Proc F…
Pune, Maharashtra, India
$950/hr · Starting at $900
• 10 years of experience in SAS programming of statistical reports, clinical database and statistical analysis for clinical trials • Have led a team of 2-3 people and worked as a POC • Experienced in
Cambridge, Cambridgeshire, United Kingdom
$70/hr · Starting at $1,000
Freelance Contract Clinical Research and Data Specialist with over 20 years experience. Clinical trial experience that spans Pharmaceutical, Biotechnology, Consumer Health and CRO working environments…
Indore, Madhya Pradesh, India
4,510/yr · 100%
$25/hr · Starting at $100
- Good Exposure in SAS Application development in Clinical Domain in MS-Windows Environment. -Experience in SAS programming with reference to Base, Access, Sql, Macros and knowledge on SAS EG and Adva…
Bucharest, Bucuresti, Romania
- working on Clinical Research field for over 5 years; - great experience in the domains:pediatrics, oncology, cardiology, infectious diseases and psychiatry; -I have done various trainings (SOPs) in…
Clondalkin, Dublin, Ireland
ID Verified
$25/hr · Starting at $500
Analytics Engineer with 3 years of experience in designing and optimizing data platform systems, ensuring data integrity, and maximizing business value through business intelligence. Key differentiato…
Hyderabad, Telangana, India
$10/hr · Starting at $25
I am Nazini having 2 yrs experience as Clinical SAS Programmer and 5 yrs experience in pharma industry in post marketing validations of formulations. Have a good understanding on regulatory guidelines…
Cary, North Carolina, United States
Having worked in the Pharmaceutical industry for over 10 years, I am well versed in working with Clinical Trial data. I provide SDTM/ADaM programming services and their validation with due respect to
Bangalore, Karnataka, India
Having around 5 years of experience in generating reports and analyzing data for clinical trials using different SAS Tools. • Good Experience in understanding the PROTOCOLS,CDISC Process, SOP’s and S…
Secunderabad, Andhra Pradesh, India
Good knowledge in Base & Advanced SAS. Generation of various SAFETY TABLES. Working on mapping of various domains. Having knowledge on phases (I-III) of clinical trials. Have good knowledge on CRF an…
Past Earnings
$15/hr · Starting at $1,000
We are a Web Development Services Company based in Pune, India empowering businesses globally to establish a strong online presence, engage their audience, and achieve their digital goals. Our team of…
$50/hr · Starting at $25
Detailed-oriented, highly-motivated Clinical Research Professional with both pharmaceutical and CRO project management experience in various therapeutic areas. Effectively manage startup, maintenance,…
Beverly Hills, California, United States
$25/hr · Starting at $25
Screening of candidates, monitoring patient progress and completing case report forms for Clinical Trials stafes II-IV. Scope of work included pre screening potential candidates by phone for qualifica…
caldicot, Wales, United Kingdom
$40/hr · Starting at $25
Creative, detail-oriented, and expert clinical project consultant with more than 15 years of experience enhancing healthcare worker practices through targeted and effective clinical quality improvemen…
Athens, Georgia, United States
$15/hr · Starting at $25
I have earned the SAS Base Certification in 2012. Have worked in the area of clinical trials for 11 years (as Clinical Research Associate and Data Associate) for pharmaceutical companies in Germany an…
Latur, Maharashtra, India
$15/hr · Starting at $45
I am here to offer services in clinical trials, pharmacovigilance, medical writing, manuscript writing, protocol writing, medical monitoring, literature review etc. All the research work has to be per…
Amersfoort, Utrecht, Netherlands
$100/hr · Starting at $100
Many years experience advising CRO`s, pharmaceutical companies, bio-tech companies, and other players within the pharmaceutical and medical device industries on the the legal issues surrounding inform…
Ahmedabad, Gujarat, India
$20/hr · Starting at $25
- More than 8 years of experience working in Clinical Research domain, expertly gathering and analyzing data for highly confidential clinical trials. - More than 5 years of experience as study lead -
Puducherry, Puducherry, India
8+ years of experience in clinical data management. Expertise in end to end data management activities. Experienced in Rave EDC. Able to perform database testing (screen and export), edit check speci…