# Sr Site ID & Feasibility Specialist

**Company**: IQVIA
**Work arrangement**: hybrid
**Experience**: senior
**Category**: Healthcare
**Industry**: Healthcare

**Apply**: https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Istanbul-Turkey/Sr-Site-ID---Feasibility-Specialist_R1568578?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply
**Canonical**: https://yubhub.co/jobs/job_58648a5e-a12

## Description

Make an impact on patient health!

IQVIA's Global Site Activation Team drives best-in-class site and customer experience, with industry-leading outcomes. The team keeps the patient at the forefront, always prioritizing their needs.

**Job Overview** Manage and lead activities associated with Feasibility and/or Site Identification for regional and/or country projects and/or programs.

**Essential Functions**

- Manage assigned opportunities/projects/programs for country or region and adhere to timelines and budget.

- Ensure the site list for assigned studies includes an adequate number of appropriate investigators in accordance with the needs of the sponsor and specifications of the protocol.

- Collect and analyze country/regional Feasibility and/or Site Identification information to meet timelines of each study.

- Attend kick-off meetings to understand study requirements, including investigator profile, protocol, process specifics, and timelines.

- Raise questions and make suggestions based on SID SOPs and Work Instructions.

- Distribute, track, negotiate, and review Confidential Disclosure Agreements (CDAs) for Feasibility and/or Site Identification with input from the study team, management, and Legal when appropriate.

- Distribute, track, and review Site Questionnaires for Feasibility and/or Site Information Forms or Site Qualification Questionnaires for SID.

- Ensure completeness, site capability, and suitability for the study.

- For SID, review SIF and/or SQQ vs the guidance document and approve for SSV or select appropriate sites.

- Manage investigator database entry and quality, ensuring complete investigator and site information is captured and monitoring for duplicate entries.

- Maintain and update company information repositories and databases.

**Qualifications**

- Bachelor's degree in Life Sciences, or a related field

- 3 years of clinical research experience in Feasibility and/or Site Identification ready to enroll activities

- Strong problem-solving skills

- Ability to negotiate and have strong communication skills

- Ability to work on multiple projects

- Knowledge of applicable functional/regulatory requirements, including local regulations, SOPs, and ICH/GCP

## Skills

### Required
- Life Sciences
- clinical research
- Feasibility
- Site Identification
- problem-solving
- communication
- negotiation
- ICH/GCP

---

Source: [Apply at iqvia.wd1.myworkdayjobs.com](https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Istanbul-Turkey/Sr-Site-ID---Feasibility-Specialist_R1568578?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply)