Site Activation Specialist

iqvia; København; On-site; DKK 520,000 - 700,000; Full time

Job summary

IQVIA's Global Site Activation Team seeks a Site Activation Specialist to act as a single point of contact for feasibility, site activation and maintenance activities across studies. You will review regulatory and contractual documents, ensure accuracy, and coordinate with the Site Activation Manager, Project Management and other departments to keep timelines on track.

Join a global network across 141 locations and engage with various therapeutic areas, leveraging innovative technologies to

Qualifications

• Bachelor’s Degree in Life Science or related field.
• 1 - 3 years’ prior experience in Life Sciences or similar.
• Ability to work independently but also collaborate.
• Good interpersonal, communication and organisational skills to establish and maintain effective working relationships with co-workers, managers and sponsors
• Ability to work on multiple projects.
• Knowledge of applicable regulatory requirements, including local regulations, SOPs and ICH/ GCP

Responsibilities

• Serve as Single Point of Contact to perform feasibility, site activation and some maintenance activities in assigned studies.
• Review documents for completeness, consistency, and accuracy under guidance of senior staff.
• Prepare site documents and inform team members of completion of regulatory contractual.
• Distribute completed documents to sites and internal project team members and update internal systems and project plans.
• Review, track, and follow up the progress, the approval and execution of required documents such as questionnaires, CDAs, regulatory, ethics, Informed Consent Form, and Investigator Pack release documents.

Skills

Independent work

Interpersonal skills

Communication skills

Organisational skills

Multi-project management

Education

Bachelor's Degree in Life Science or related field

Job description

Site Activation Specialist:

Country Site Activation - CSA

Make an impact on patient health! IQVIA’s Global Site Activation Team of 2000 employees, drives best in class site and customer experience, with industry leading outcomes. We keep the patient at the forefront; ‘Always Impatient for the Patient’ and we excel in our collaboration with our external/internal customers. IQVIA’s Country Site Activation team are a global network who identify and activate sites to the highest quality to ensure patients on Clinical trials have access to safe and effective medication. We are leaders in innovation and first to new technologies, meaning a vast amount of career development opportunities are available.

Job Overview:

As a Site Activation Specialist, you will serve as a Single Point of Contact to perform feasibility, site activation and some maintenance activities in assigned studies for investigative sites, according to applicable regulations, SOPs and work instructions, working closely with the Site Activation Manager, Project Management team, and other departments as necessary. You will review documents for completeness, consistency, and accuracy, under guidance of senior staff and prepare site documents, inform team members of completion of regulatory contractual. Along with distributing completed documents to sites and internal project team member and updating and maintaining internal systems, databases, tracking tools, timelines, and project plans with accurate and complete project specific information. You will also review, track, and follow up the progress, the approval and execution of required documents such as questionnaires, CDAs, regulatory, ethics, Informed Consent Form, and Investigator Pack release documents.

Requirements:

• Bachelor’s Degree in Life Science or related field
• 1 - 3 years’ prior experience in Life Sciences or similar (or equivalent combination of education, training and clinical, healthcare and/or pharma experience)
• Ability to work independently but also collaborate with others
• Good interpersonal, communication and organisational skills to establish and maintain effective working relationships with co-workers, managers and sponsors
• Ability to work on multiple projects
• Knowledge of applicable functional/regulatory requirements, including local regulations, SOPs and ICH/ GCP

Join IQVIA and let’s create a healthier world together:

• Exposure across 21 Therapeutic Areas
• Be part of a global team who operate across 141 locations
• Exposure across a variety of studies and projects
• Access to new, innovative technologies
• Work within a collaborative and vibrant environment
• Own your career!

Unleash your potential! It takes passion to make the extraordinary possible for patients. Our culture of innovation and collaboration enables us to explore new possibilities and help improve health around the world. When you join our diverse, global team, you’ll harness the power of unparalleled data, advanced analytics, cutting-edge technologies, and deep healthcare and scientific expertise to drive healthcare forward.

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 committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.