New Delhi, Delhi, India
$9/hr · Starting at $26
I want to do some clinical trials. Along with clinical trials I can manage all the data of the clinical trial. I have done Btech in Biotechnology.
wixom, Michigan, United States
ID Verified
$50/hr · Starting at $50
We offer complete clinical trial management services to sites, CROs, and Sponsors. We have a team of medical professionals with experience at all levels of trials to maintain efficiency and meet dead…
Chopda, Maharashtra, India
$200/hr · Starting at $150
i have 2 year of experience in data entry and typing field of clinical research. handle patient data and clean patient files
Pune, Maharashtra, India
$10/hr · Starting at $25
Study setup, conduct and closeout. Vaccine, rare disease clinical trials. Inform 4.6, Oracle Clinical and Rave
Ambala, Haryana, India
$50/hr · Starting at $2,000
Clinical data analyst, Toxicologist, medical writing, clinical research, post market surveillance, clinical Pharmacist
Hyderabad, Telangana, India
10 years of varied clinical experience which includes clinical Data & Project Management. Adept at handling multiple projects efficiently and deliver tasks within specified timelines Planning, manage
Thiruvarur, Tamil Nadu, India
$30/hr · Starting at $100
having 07 years of experience in clinical research. I have worked in various department like clinical operation (CRA and site monitoring), medical writing (preparation of Clinical study protocol, Info…
Lisboa, Lisboa, Portugal
$5/hr · Starting at $25
Liason with quality team, production team, clinical team (~20 people) - Lifecycle management of Medicinal Products for Human use, Skills on Regulatory affairs (EudraLex Vol.2), Market access, Pharmaco…
Bangalore, Karnataka, India
$18/hr · Starting at $25
Over 3 years of experience in programming clinical trial data by using SAS 9.X versions.Hands on Experience in using SASSTAT, /BASE, SAS/SQL, SAS/ MS-EXCEL. Responsible for Developing reports for Safe…
Mumbai, Maharashtra, India
$15/hr · Starting at $25
I have 14 years of experience in CDM. I have worked as CRF Designer, Database developer, Lead data Manager, and Project data Manager. I have worked on multiple CDMS such as Oracle Clinical, Oracle RDC…
Tbilisi, T'bilisi, Georgia
$12/hr · Starting at $30
I want to do Clinical Trials. Iam Medica Doctor, PhD. Experienced Senior CRA with a demonstrated history of working in the pharmaceuticals industry. I have had advanced for the full monitoring of act…
$10/hr · Starting at $50
Experience – Clinical SAS Programmer with over nine years (9) of experience in Pharmaceutical industry, with strong background in Clinical Trials, end-to-end Clinical Study Reporting, CDISC Data Stand…
Los Angeles, California, United States
- Worked in collaboration with Principal Investigators, Sub-Investigators and staff to prepare new clinical trials to be submitted to the Institutional Review Board including but not limited to protoc…
$15/hr · Starting at $30
1. Clinical Regulatory Services Clinical Trial Submissions Clinical Study Design Sample Size Estimation Protocol Synopsis Protocol Development Informed Consent Form Advertising Material Insurance and
Hampton, New Hampshire, United States
Skills with clinical trial conduct and research regulations. Have 6 years experience with clinical research studies and sound understanding of regulations.
Virar - Bolinj, Maharashtra, India
I am an experienced Clinical Researcher/Healthcare professional based in Mumbai and have around 10 years of experience working in Clinical Research, Clinical Trials, Scientific writing, Project Manage…
Hosur, Tamil Nadu, India
Have 3+ years of experience in clinical trials and worked with top MNC clients and have decent knowledge about ICH-GCP
Silver Spring, Maryland, United States
$80/hr · Starting at $25
LAH Clinical is a Consulting Research Organization that provides clinical research, administrative, medical and scientific services to pharmaceutical and biotechnology companies, private organizations…
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…
$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…