Reading, England, United Kingdom · On-site
To lead Local Study Teams (LSTs) at country level to deliver committed components of clinical studies according to agreed resources, budget and timelines complying with Sponsor Procedural Documents, international guideli…
Skills: Clinical Trial Management, ICH-GCP, Project Management, Site Monitoring, Risk Management
Reading, England, United Kingdom · On-site
This role contributes to the development of Oracle's globally harmonized EHS management system and owns its deployment across EMEA, along with regulatory compliance across EMEA jurisdictions and end-to-end EHS oversight …
Skills: EHS Leadership, Regulatory Compliance, ISO 45001, ISO 14001, Incident Management
Reading, England, United Kingdom · On-site
As our Aftercare Coordinator, you will work on our PRS platform focused on single family housing. You will be responsible for supporting the Aftercare/defects team on a selection of the Leaf portfolio (to be regionalised…
Skills: Customer Service, Defect Management, Communication, Stakeholder Management, Project Coordination
Reading, England, United Kingdom · On-site
The Block Manager is responsible for the day-to-day management and performance of residential apartment buildings, ensuring they are safe, compliant, and well maintained. The role has a strong focus on health and safety …
Skills: Residential Block Management, Health & Safety Compliance, Budget Management, Contractor Management, Stakeholder Management
Reading, England, United Kingdom · On-site
Company Description Trading Lead Because your perspective shapes trends. Innovate, your way. The Trading Lead role works in partnership with our Central Trade & Planning Team, BMD, and Commercial Retail functions as well…
Skills: Pricing & Promotions, Markdown Management, Licence Management, Campaign Management, Data Analysis
Reading, England, United Kingdom · On-site
Exceptional Hospitality Starts with You Picture yourself brightening someone’s day. When you join Hilton Reading, that’s exactly what you’ll do every time you come to work! As an Assistant Night Manager, you’re not just …
Skills: Hospitality Management, Financial Operations, Leadership, Teamwork, Guest Experience
Reading, England, United Kingdom · On-site
Team Leader Ventilation Hygiene Engineer – Grease Extraction & Fire Damper Testing Location: Reading / Slough / Bracknell and surrounding areas Salary: £32,500 + overtime + bonus Hours: Days and Nights - 10 hour days (in…
Skills: Ventilation Hygiene, Fire Damper Testing, Grease Extraction, Ductwork Cleaning, Team Leadership
Reading, England, United Kingdom · On-site
Team Leader Ventilation Hygiene Engineer – Grease Extraction & Fire Damper Testing Location: Reading / Slough / Bracknell and surrounding areas Salary: £32,500 + overtime + bonus Hours: Days and Nights - 10 hour days (in…
Skills: Ventilation Hygiene, Fire Damper Testing, Ductwork Cleaning, Team Leadership, TR19 Grease Standards
Reading, England, United Kingdom · On-site
Team Leader Ventilation Hygiene Engineer – Grease Extraction & Fire Damper Testing Location: Reading / Slough / Bracknell and surrounding areas Salary: £32,500 + overtime + bonus Hours: Days and Nights - 10 hour days (in…
Skills: Ventilation Hygiene, Fire Damper Testing, Ductwork Cleaning, Team Leadership, Grease Extraction
Reading, England, United Kingdom · Remote OK
This is where your work makes a difference. At Baxter, we believe every person—regardless of who they are or where they are from—deserves a chance to live a healthy life. It was our founding belief in 1931 and continues …
Skills: Marketing, Medical Devices, Sales, Strategic Planning, Product Marketing
Reading, England, United Kingdom · On-site
IQVIA Medical Communications is seeking an Associate Director, Client Services to drive growth, quality and customer relationships across account(s) in our global business. Who We Are IQVIA is a global leader in bringing…
Skills: Client Services, Account Management, Business Development, Financial Performance, Strategic Planning
Reading, England, United Kingdom · On-site
International. Sport enthusiasts. Collaborative team members. Stronger together through our driving force to move people through the wonders of sport. At Decathlon UK and Ireland, we offer Careers That Let You Play. As p…
Skills: Retail Management, Customer Excellence, Stock Management, P&L Management, Team Leadership
Reading, England, United Kingdom · Hybrid
Wood is currently looking to recruit a Principal Rotating Equipment Engineer to undertake a Project Management Consultant role on the EPC phase of a Major Middle East Oil and Gas Development Project. This is a 6 month co…
Skills: Rotating Equipment Engineering, Project Management Consulting, Pumps, Compressors, FEED
Reading, England, United Kingdom · On-site
Established in 1981 with a single store in the Northwest of England, the JD Group is a leading omni-channel retailer of Sports Fashion, Outdoors and Gyms with our colleagues working in stores across several retail fascia…
Skills: Leadership, Team Development, Retail Operations, Customer Service, Commercial Awareness
Reading, England, United Kingdom · On-site
Project Manager L1 Band: B3/C1 Location: Reading, United Kingdom Position: 1 Role Summary · Provide senior project leadership and governance oversight for the ServiceNow CSDM-aligned re-platforming program in an onshore …
Skills: Project Management, Program Governance, Stakeholder Management, ServiceNow CSDM, RAID Management
Reading, England, United Kingdom · Hybrid
Location: Reading, United Kingdom Thales is a global technology leader with more than 83,000 employees on five continents. With over 7,500 people in the UK, operating across defence, space, aerospace, and digital securit…
Skills: Bid Management, Commercial Acumen, Stakeholder Management, Proposal Writing, Cost Estimation
Reading, England, United Kingdom · On-site
Job Overview Join LKQ UK & Ireland as a Driver Coordinator and play a key role in keeping our delivery operations running smoothly. You’ll manage driver schedules, support the team, and ensure our customers receive their…
Skills: Route Planning, Team Leadership, Customer Service, Health and Safety Compliance, Cost Control
Reading, England, United Kingdom · Hybrid
Sr CRA ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven organisation, integrity, collaboration, …
Skills: Clinical Trial Monitoring, Good Clinical Practice (GCP), Site Management, Data Integrity, Stakeholder Management
Birmingham, England, United Kingdom · Hybrid
At EY, you’ll have the chance to build a career as unique as you are, with the global scale, support, inclusive culture and technology to become the best version of you. And we’re counting on your unique voice and perspe…
Skills: Employment Tax, Expenses & Benefits, Employment Status, Payroll, Construction Industry Scheme
Reading, England, United Kingdom · On-site
$13/hr–$14/hr
Job Description: Senior Care Assistant Location: Parkside Care Home, Parkside Road, Reading RG30 2DP Contract: Permanent - Full Time Hours: 44 hours per week, covering days and nights Salary: £13.25 - £14.84 per hour dep…
Skills: Clinical Duties, Medication Administration, Care Planning, Team Management, Staff Supervision
Sign up with Clera and we'll reach out the moment a role actually fits you — no more spraying applications into the void.
Lead Local Study Teams to deliver clinical study components according to budget, timelines, and regulatory guidelines. Oversee site identification, qualification, monitoring, and the archiving of essential documentation.
Requires a bachelor's degree in life sciences and at least 3 years of experience in development operations or related fields. Must possess strong knowledge of ICH-GCP, clinical study processes, and therapeutic areas such as Oncology or Cardiology.
To lead Local Study Teams (LSTs) at country level to deliver committed components of clinical studies according to agreed resources, budget and timelines complying with Sponsor Procedural Documents, international guidelines such as ICH-GCP as well as relevant local regulations. In addition to leading LST(s), the Local Study Associate Director may perform site monitoring as needed to support the flexible capacity model.
The Local Study Associate Director is responsible to ensure that sites are identified, site qualifications performed, set up, initiated, monitored, closed and documentation archived.
Has the overall responsibility for the study commitments within the country and for timely delivery of data to required quality.
Leads Local Study Team consisting of CRA(s), CSA(s), for assigned study/studies
Leads and optimises the performance of the Local Study Team(s) at country level ensuring compliance with Sponsor Procedural Documents, ICH-GCP and local regulations.
Ensures, as required, that clinical and operational feasibility assessment of potential studies is performed to the highest quality.
Coordinates the site selection process by identifying potential sites/investigators, performing initial Site Quality Risk Assessment, and conducting Site Qualification Visits to evaluate suitability and quality risks.
Ensures timely submission of application/documents to EC/IRB at start up and for the duration of the study. Works together with Regulatory Affairs to ensure timely delivery of application/documents for submissions to Regulatory Authority for the duration of the study, and in line with local regulations.
Ensures timely preparation of country financial Study Management Agreement (fSMA) and maintains accurate study budget in Sponsor clinical studies financial system by regular checks of the system and financial reports (as agreed with Director, SMM/ Director, Country Head.
Ensures timely preparation of local Master CSA (including site budget) and amendments as needed.
Ensures timely preparation of country level Master Informed Consent Form (MICF) and subsequent site level ICFs, as required, including any relevant translations, and in line with relevant Sponsor SOPs and local regulations.
Ensures all country and site level trial essential documents required by ICH-GCP prior to study start have been collected and verified for correctness, prior to setting sites ready to enrol, and in line with Sponsor SOPs.
Plans and coordinates applicable local drug activities (from local purchase or reimbursement to drug destruction).
Sets up and maintains the study in CTMS at study country level as well as local websites as required by local laws and regulations.
Oversees, manages and coordinates monitoring activities from site activation through to study closure at country and site level in accordance with the Monitoring Plans.
Reviews monitoring visit reports (as required and following Sponsor SOPs) and pro-actively advices the monitor(s) on study related matters.
Performs any required co-monitoring, Accompanied Site Visits/training visits with study CRAs.
Proactively identifies risks and facilitates resolution of complex study problems and issues.
Organises regular Local Study Team meetings on an agenda driven basis.
Actively works towards achieving good personal relationships with all Local Study Team members, sites’ staff and global stakeholders.
Reports study progress/update to the Global Study Associate Director/ Global Study Team including SMM Lead.
Contributes to patient recruitment strategy including regular communication with participating Investigators as necessary.
Develops, maintains and reviews risk management plan on country study level: proactively manages sites, stakeholders, local and global vendors and customers to ensure risks are timely identified, mitigated and managed.
Communicates and co-ordinates regularly with National Co-ordinating Investigator / National Lead Investigator on recruitment and other study matters, if applicable.
Plans and leads National Investigator meet Ensures that all study documents are ready for final archiving and completion of local part of the eTMF.
Plans and leads activities associated with audits and regulatory inspections in liaison with CQAD and QA.
Provides input to process development and improvement.
Provides regular information to Line Managers at country level on study and planned study milestones/key issues.
Updates Line Managers about the performance of the CRAs/CSAs.
Ensures that study activities at country level comply with local policies and code of ethics.
Provides feedback on any research related information including sites/investigators/competing studies that might be useful for the local market.
Ensures compliance with Sponsor´s Code of Ethics, company policies and procedures relating to people, finance, technology, security and SHE (Safety, Health and Environment).
Collaborates with local Medical Affairs team.
Supports SMM in different initiatives (local, regional or global) as agreed with the SMM Line Management.
Bachelor degree in related discipline, preferably in life science, or equivalent qualification.
Minimum 3 years of experience in Development Operations (CRA, Sr CRA) or other related fields (Medical Affairs-led or Academic-led studies).
Good knowledge of international guidelines ICH GCP as well as relevant local regulations.
Proven ability to lead and motivate cross functional teams to deliver clinical trials according to or ahead of time plan, budget and with required quality.
Good medical knowledge of Oncology, Rare Diseases, cardiology, hematology, CVRM Therapeutic Areas.
Good knowledge of the Drug Development Process.
Excellent understanding of the Clinical Study Process including monitoring.
Very good understanding of the Study Drug Handling Process and the Data Management Process.
Excellent project management skills.
Excellent ability to prioritize and handle multiple tasks, attention to details and negotiation skills.
Excellent knowledge of spoken and written English.
Good ability to learn and to adapt to work with IT systems.
Ability to travel nationally and internationally as required.
Please note: due to sponsor requirements for the role only candidates based in the listed location/s will be considered. Any applications from candidates based outside of these locations will not be considered.
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.
IQVIA (NYSE:IQV) is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. IQVIA’s portfolio of solutions are powered by IQVIA Connected Intelligence™ to deliver actionable insights and services built on high-quality health data, Healthcare-grade AI™, advanced analytics, the latest technologies and extensive domain expertise. With approximately 88,000 employees in over 100 countries, including experts in healthcare, life sciences, data science, technology and operational excellence, IQVIA is dedicated to accelerating the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. IQVIA is a global leader in protecting individual patient privacy. The company uses a wide variety of privacy-enhancing technologies and safeguards to protect individual privacy while generating and analyzing information on a scale that helps healthcare stakeholders identify disease patterns and correlate with the precise treatment path and therapy needed for better outcomes. IQVIA’s insights and execution capabilities help biotech, medical device and pharmaceutical companies, medical researchers, government agencies, payers and other healthcare stakeholders tap into a deeper understanding of diseases, human behaviors and scientific progress, in an effort to advance healthcare. To learn more, visit www.iqvia.com.
Offices: 2400 Ellis Rd, Durham, North Carolina 27703, US
There are currently 321 open management & leadership positions in Reading, United Kingdom listed on Clera. New openings are added daily as companies post roles.
Companies currently hiring include Primark, PepsiCo, EY, IQVIA, ICON plc, among others. Browse the listings above to see every active employer.
Yes — 172 of the 321 open management & leadership positions offer remote or hybrid work (25 remote, 147 hybrid).
Each listing links directly to the employer's application page. Apply early — fresh listings get the most recruiter attention in the first two weeks.
