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…
Hyderabad, Telangana, India
$8/hr · Starting at $25
I have good exposure in clinical research activities. I have good knowledge of ICH GCP guidelines and all the phases of clinical trials. Protocol writing and analysis of safety and efficacy of drug in…
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
4,782/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…
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…
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…
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…
$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…
London, England, United Kingdom
$45/hr · Starting at $45
A focused and driven individual with extensive experience in problem solving and building scalable software and AI systems for a range of different industrial sectors. Have experience managing and sca…
Kragujevac, Serbia, Serbia
ID Verified
$30/hr · Starting at $500
Someone said that software deployment (go live) is just the end of the beginning. There are always new ideas for additional features, improvements, dashboards, reports… We can offer maintenance of you…
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…
Kharagpur, West Bengal, India
Experience of working for 2.1 years as Junior Regulatory Associate at Parexel International, Bangalore. Possess analytical skills and ability to interpret statistical and scientific data. Possess high…
$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…