Site Activation Coordinator at IQVIA. - Turkey

Dalian, Liaoning, China -

Full Time

Start Date

Immediate

Expiry Date

08 Feb, 26

Salary

0.0

Posted On

10 Nov, 25

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Interpersonal Communication, Organizational Skills, Word Processing, MS Office, Attention to Detail, Clinical Trial Awareness, Project Management, Regulatory Document Preparation

Industry

Hospitals and Health Care

Description

with site activation activities in accordance with applicable local and/or international regulations, standard operating procedures (SOPs), project requirements and contractual/budgetary guidelines. May also include maintenance activities. Essential Functions • Under general supervision, perform site activation activities in assigned studies for investigative sites, according to applicable regulations, SOPs and work instructions, working closely with the Site Activation Manager (SAM), Project Management team, and other departments as necessary. Review documents for completeness, consistency and accuracy, under guidance of senior staff. • Prepare site regulatory documents, reviewing for completeness and accuracy. • Inform team members of completion of regulatory and contractual documents for individual sites. • Distribute completed documents to sites and internal project team members. • Support the updating and maintenance of internal systems, databases, tracking tools, timelines and project plans with accurate and complete project specific information. • Review, track and follow up the progress, the approval and execution of documents, regulatory, ethics, Informed Consent Form (ICF) and Investigator Pack (IP) release documents. Qualifications • Bachelor's Degree Life sciences or a related field . Pref • 1 years’ experience in a healthcare environment or equivalent combination of education, training and experience. Productive individual contributor who works under general supervision. Problems faced are generally routine but may require interpreting proceedures or policies to resolve. • Good interpersonal communication and organizational skills. • Good word processing skills and knowledge of MS Office applications. • Good attention to detail. • General awareness clinical trial environment and drug development process. • Ability to work on multiple projects. • Ability to establish and maintain effective working relationships with co-workers, managers and sponsors. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide. To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.

How To Apply:

Incase you would like to apply to this job directly from the source, please click here

Responsibilities

Perform site activation activities for investigative sites according to regulations and SOPs. Support the preparation and distribution of regulatory documents and maintain project-specific information in internal systems.