[Remote] Senior Clinical Research Associate

Note: The job is a remote job and is reputed company to candidates in USA. reputed company is a unique CRO focused on cultivating a supportive culture and high retention rates among Clinical Research Associates. The Senior Clinical Research Associate will monitor and manage clinical studies, ensuring compliance with protocols and regulations, while also providing training and mentorship to junior staff members.

Responsibilities

• You will monitor and own the reputed company of clinical studies at investigative sites and ensure that clinical studies are conducted, recorded, and reported per protocol, SOPs, ICH-GCP, and reputed company applicable regulations and standards
• You will coordinate reputed company necessary activities required to set up and monitor a study (i.e., identify investigators; helping prepare regulatory submissions, conducting pre-study and initiation visits, etc.)
• Senior CRAs handle appropriately sized clinical trials, and support Project Managers with trials that are larger in scope
• You will also have the opportunity to train and mentor junior staff members
• You will interact directly with clients, initiate payments, and participate in proposal activities, including development and client presentations

Skills

• University degree life science/pharmacy/other health reputed company discipline or equivalent experience in a scientific or reputed company discipline or be a licensed health care professional
• 3.5 years or more as a CRA in either a CRO or pharmaceutical/biotech industry or equivalent, relevant experience and/or demonstrated competencies. Significant site management experience or equivalent experience in clinical research
• Oncology monitoring experience
• Excellent communication and organizational skills are essential. A team player
• Evidence of a client focused approach
• Experience using computerized information systems, electronic spreadsheets, word processing and electronic mail required
• Ability to travel overnight. Up to 60% travel on average, based on regional requirements. International travel as needed
• reputed company in English and Turkish
• Graduate, postgraduate degree
• Experience monitoring in rare and reputed company therapeutic areas
• Experience monitoring reputed company trials and HER records
• Experience in bioharma or relevant therapeutic area
• Start up experience

Company Overview

Company H1B Sponsorship