Study Start Up Specialist (UK, homebased), IQVIA Biotech

IQVIA; Remote; GBP 35,000 - 50,000; Full time

Job summary

A leading global provider of clinical research services is seeking a Study Start-Up Specialist for a UK homebased position. This role involves leading Site Activation activities, ensuring compliance with regulations, and managing site documentation. Candidates should have a Bachelor’s Degree in life sciences, 3 years of clinical research experience, and strong communication skills. Join a dynamic team to contribute to innovative medical treatments and improve patient outcomes.

Benefits

Exposure across 21 Therapeutic Areas

Access to innovative technologies

Collaborative working environment

Qualifications

• Minimum 3 years of clinical research experience, including 1 year in leadership.
• In-depth knowledge of clinical systems, procedures, and corporate standards.
• Knowledge of GCP/ICH and applicable regulatory guidelines.

Responsibilities

• Lead Site Activation activities according to regulations.
• Prepare site documents and ensure their accuracy and completeness.
• Review and track progress of regulatory documents.

Skills

Clinical research experience

Negotiating skills

Communication skills

Organizational skills

Education

Bachelor’s Degree in life sciences or related field

Job description

Study Start Up Specialist (UK, homebased), IQVIA Biotech page is loaded## Study Start Up Specialist (UK, homebased), IQVIA Biotechlocations: Stafford, United Kingdomtime type: Full timeposted on: Posted Todayjob requisition id: R1513877**Study Start-Up Specialist****IQVIA Biotech****UK Homebased****Job Overview**Perform tasks at a country level associated with Site Activation (SA) 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*** As a Study Start-Up Specialist, you will work and lead complex projects under general supervision, serve as Single Point of Contact in assigned studies for investigative sites, Site Activation Manager, Project Management team, and other departments as necessary.* You will also ensure adherence to standard operating procedures (SOPs), Work Instructions, quality of designated deliverables and project timelines.* You will perform feasibility, site ID, start up and site activation activities according to applicable regulations, SOPs and work instructions, along with distributing completed documents to sites and internal project team members.* You will also prepare site documents and review for completeness and accuracy, along with reviewing, tracking, and following up the progress, the approval and execution of documents, questionnaires, CDA/SIF, regulatory, ethics, Informed Consent Form, and Investigator Pack release documents, in line with project timelines.* Coupled with informing team members of completion of feasibility, site ID, regulatory and contractual documents for individual sites, and providing local expertise to SAMs and project team during initial and on-going project timeline planning. Along with performing quality control of documents provided by sites.* You may also act as an SME on specific subjects, mentor junior CSAs, and have a sponsor-facing role.**Qualifications and Skills*** Bachelor's Degree Bachelor’s Degree in life sciences or a related field* 3 years clinical research experience, including 1 year experience in a leadership capacity.* In-depth knowledge of clinical systems, procedures, and corporate standards.* In-depth knowledge of submissions for UK and Ireland* EUCTR knowledge* Good negotiating and communication skills with ability to challenge, if applicable.* Effective communication, organizational, and interpersonal skills.* Ability to work independently and to effectively prioritize tasks.* Ability to manage multiple projects.* Knowledge and ability to apply GCP/ICH and applicable regulatory guidelines.* Knowledge of applicable regulatory requirements, including local regulations, , SOPs and company’s Corporate Standards.* Understanding of regulated clinical trial environment and knowledge of drug development process.* Ability to establish and maintain effective working relationships with coworkers, managers and clients.**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 atIQVIA 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.