Immediate opening for Clinical Researcher having Weka Report skill

Immediate opening for Clinical Researcher having intern experience of min. 2 years

If your profile matches to the below requirement, send your resume to career@credencease.com with subject line in the format : <"Clinical Researcher"><space><your name>

Overview: :
The Clinical Research Associate (CRA) will monitor the progress of clinical studies at investigative sites or remotely, and ensure clinical trials are conducted, recorded, and reported in accordance with the protocol, standard operating procedures (SOPs), ICH-GCP, and all applicable regulatory requirements.

Experience: 

• Experience in monitoring all trial components (PSSV to COV)
• 2+ years of clinical monitoring experience required.

Qualifications:
Graduate / Undergraduate degree or its international equivalent in clinical, science, or health-related field from an accredited institution;

Skill Required: 

• Should have worked on Algorithm data (Mandatory)
• Should have the technical knowledge of WEKA reports making along with Formulations and clustering. (Mandatory)
• Clinical research experience
• Excellent written and oral communication
• Ability to manage investigative sites to facilitate trial deliverables

Details Job Description:

• Conducts monitoring to confirm subject safety and data integrity
• Describes and demonstrates the principals of IP accountability
• Identifies scientific misconduct at the site level
• Demonstrates working knowledge of Microsoft Office applications, Clinical Trial Management Systems, IVRS/IWRS and Electronic Data Capture platforms
• Mentors CRAs new to the position or company
• Serves as an observation visit leader
• Conducts monitoring evaluation visits 
• Assists team lead in the development of trial tools or documents

Salary: As per industry standard

Industry: Biotech / Clinical Research / ITES

Functional Area:Medical , Healthcare , R&D , Pharmaceuticals , Biotechnology

Role Category:R&D

Role:Clinical Research Associate/Scientist