JUMP TO CONTENT

Site Selection Specialist

  1. Ankara
JR121087
  1. Study Start Up
  2. ICON Full Service & Corporate Support

About the role

This vacancy has now expired. Please click here to view live vacancies.

Site Selection Specialist

ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.

We are currently seeking Site Selection Specialist to work with the Site Identification Lead to ensure knowledge of the goals, scope and requirements of the Site Identification project (e.g. number of sites required/country, number of positive responses required etc.) and ensure that high quality results are delivered.

The role:

The Site Selection Specialist will contact and build relationships with study investigators/sites and networks in assigned areas for the conduct of feasibility and potential study participation.

Role Responsibilities:

Work with the Site Selection Lead to ensure knowledge of the goals, scope and requirements of the project (e.g. number of sites required/country, number of positive responses required etc.) and ensure that high quality results are delivered.

Identify study investigators/ sites for potential study participation, both from the database and other potential sources such as local intelligence/internet etc. Ensure all newly identified sites are data based appropriately, checked for quality status and are fully processed.

To contact and build relationships with study investigators/ sites and networks in assigned areas (e.g. region(s), countries I countries or therapeutic area) for the conduct of feasibility and potential study participation.

To perform phone selection visits, if required.

To liaise with country managers to gather country specific evidence to support Site Selection, e.g. site list review, country specific profile of sites, standard of care.

To ensure that all data collected, in the conduct of Site Selection or site related country feasibility, is fully documented and kept up to date in relevant systems to build knowledge and intelligence.

To ensure appropriate procedures are followed, whether Sponsor specific or according to ICON SOPs, Site Selection RACI.

Ensure appropriate follow up with sites on any inconsistencies in data provided for analysis and to chase outstanding feasibility data to ensure a complete data set

To contact investigators, local ICON employees and collect data to support country choice in the conduct of feasibility assessment

To become a country expert on the investigator profile, healthcare setting, standard of care to ensure the best sites are approached for project

To liaise cross-functionally with other departments such as Study Start Up, CRA management to get local intelligence on sites and support local data collection

Be an expert on how to interact with sites and obtain relevant information to support Site Selection.

Use knowledge and experience to build efficiency in the process and consistently deliver high quality investigators, sites, and other data to the Functional Lead for your projects.

Ensure debarred Investigators are not included in feasibilities or for study participation.
Also ensure relevant parties, such as Site Selection lead, Feasibility Manager or Project Manager are aware of any Audit or Regulatory findings that may influence reasons for site selection.

Ensure confidentiality is maintained or appropriate confidentiality agreements are in place prior to study discussions

Ensure all investigator feedback and status of contact with the site is tracked and data based appropriately, including reasons for site selection /de-selection

Support other team members, e.g. seconded CRAs, on how to get the best information from sites, act as a trainer and mentor to new staff within the group.

Identify high performing sites and develop relationships with them as a single point of contact during site selection and ensure that key data collected from/related to these sites are maintained in ICON's systems.

Deliver high quality standards and strive for excellence, act in a proactive, flexible and responsive manner to both internal and external customer needs.

• Establish good relationships internally and externally

• To undertake other reasonably related duties as may be assigned from time to time

• Recognize, exemplify and adhere to ICON's value, which centers around our commitment to People, Clients and Performance

To embrace and contribute to our culture of process improvement with a focus on accelerating concept to cure.

• Travel (approximately 10%) domestic and/or international, as required*

Your profile:

• Bachelor´s degree in a scientific or healthcare-related field

• Prior experience in clinical research or healthcare, preferably in a CRO or pharmaceutical company

• Strong organizational and multitasking skills, with the ability to prioritize tasks and meet deadlines in a fast-paced environment

• Excellent attention to detail and accuracy in documentation

• Effective communication and interpersonal skills, with the ability to collaborate effectively with cross-functional teams and external stakeholders

#LI-SK1

What ICON can offer you:
Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent.

In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.

Our benefits examples include:

  • Various annual leave entitlements
  • A range of health insurance offerings to suit you and your family’s needs.
  • Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
  • Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family’s well-being.
  • Life assurance
  • Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others.

Visit our careers site to read more about the benefits ICON offers.

At ICON, diversity, inclusion & belonging are fundamental to our culture and values. Our rich diversity makes us more innovative which helps us better serve our people, patients, customers, and our communities. We're proud of our diverse workforce and the work we’ve done to become a more inclusive organisation. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.

If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here

Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles.

Are you a current ICON Employee? Please click here to apply

List #1

Day in the life

Similar jobs at ICON

Study Start Up Associate I

Salary

Location

Argentina, Buenos Aires

Location

Buenos Aires

Remote Working

Office Based

Business Area

ICON Full Service & Corporate Support

Job Categories

Study Start Up

Job Type

Permanent

Description

Responsibilities: Proficient knowledge of ICON SOPs/WPs, ICH/GCP and applicable country regulations/guidelines and ICON systems.Support Site Partners to collect, review, organize and assemble initial

Reference

JR140021

Expiry date

01/01/0001

Florencia Pistolesi Read more Shortlist Save this role
Study Start Up Associate II

Salary

Location

Mexico, Mexico City

Location

Sao Paulo

Mexico City

Remote Working

Office or Home

Business Area

ICON Full Service & Corporate Support

Job Categories

Study Start Up

Job Type

Permanent

Description

We are currently seeking a Study Start Up Associate II to join our diverse and dynamic team. As a Study Start Up Associate II at ICON, you will play a pivotal role in leading the initiation of clinica

Reference

JR140224

Expiry date

01/01/0001

Olivia Molina

Author

Olivia Molina
Read more Shortlist Save this role
Study Start up Associate II - Regulatory

Salary

Location

Bulgaria, Sofia

Location

Sofia

Prague

Budapest

Warsaw

Lisbon

Bucharest

Barcelona

Madrid

Bratislava

Remote Working

Office or Home

Business Area

ICON Full Service & Corporate Support

Job Categories

Study Start Up

Job Type

Permanent

Description

We are seeking a Study Start Up Associate II to join our diverse and dynamic team. In this role, you will be at the frontline of clinical research, driving the initiation of studies that bring innovat

Reference

JR144292

Expiry date

01/01/0001

Magda Kozuszek Read more Shortlist Save this role
Study Start Up Associate II

Salary

Location

Regional Great Britain (Northern Ireland)

Location

Belfast

Remote Working

Remote

Business Area

ICON Strategic Solutions

Job Categories

Study Start Up

Job Type

Permanent

Description

We are currently seeking a Study Start Up Associate II to join our diverse and dynamic team. As a Study Start Up Associate II at ICON, you will play a pivotal role in leading the initiation of clinica

Reference

JR144029

Expiry date

01/01/0001

Keri Marshall

Author

Keri Marshall
Read more Shortlist Save this role
Manager of Study Start Up

Salary

Location

UK, Reading

Location

Reading

Remote Working

Remote

Business Area

ICON Strategic Solutions

Job Categories

Study Start Up

Job Type

Permanent

Description

We are currently seeking a Manager, Study Start-Up to join our diverse and dynamic team. This position serves as an expert in Study Start Up (SSU) activities and strategy including the use of various

Reference

JR143524

Expiry date

01/01/0001

Rajvir Samra

Author

Rajvir Samra
Read more Shortlist Save this role
Site Activation Lead

Salary

Location

Poland, Warsaw

Location

Sofia

Prague

Budapest

Riga

Vilnius

Warsaw

Lisbon

Bucharest

Barcelona

Madrid

Bratislava

Tbilisi

Remote Working

Office or Home

Business Area

ICON Full Service & Corporate Support

Job Categories

Site Activation

Job Type

Permanent

Description

At ICON, study start-up is not a checklist — it’s the moment where strategy becomes access. As a Site Activation Lead, you ensure clinical trials move from plan to reality without unnecessary delays,

Reference

JR144253

Expiry date

01/01/0001

Magda Kozuszek Read more Shortlist Save this role
View Jobs

Browse popular job categories below or search all jobs above