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CTS Project Executive Company & Role Description Founded in 2002, Tanner Pharma Group is a specialty service provider in the biopharmaceutical industry focused on improving patient access to medicines on a global basis. Tanner Pharma offers its biopharmaceutical partners a portfolio of four distinct service offerings that span the product lifecycle from clinical development to commercialization. With its global headquarters in Charlotte, North Carolina and offices in the United Kingdom, Switzerland and Ireland, Tanner Pharma is in a phase of rapid growth. The Project Executive is responsible for ensuring success and completion of CTS projects, supporting the Project Manager, liaising with customers and suppliers to guarantee complete satisfaction. To support our Clinical Trial Services (CTS) department using solid project management and key account management skills to successfully see a project through to completion and to achieve Clinical Trial Supply (CT) group sales target (AOP). Role Accountabilities Expected Responsibilities for the CTS Project Executive are: Customer Account and Sales Operation Management • Provide proactive communication and excellent customer service to build and nurture client loyalty, trust, and satisfaction., • Working with the Project Managers and Snr Director to ensure the accurate and successful delivery of CTS projects against agreed KPIs and timeframes., • Prompt effective response time for internal and external communication., • Effective handling of all sales activities from order enquiry through to shipment., • Resolve queries and complaints in accordance with TPG SOPS or inform PM and Snr CTS Director in a timely manner., • Liaise with vendors to elevate competitive advantage through value and sourcing solutions., • Develop and maintain CTS Vendor database., • Liaise with customers to ensure timely and accurate delivery of projects., • Ensure all Customer records and Trackers are accurate and up to date with all CT projects and related information., • Maintain all documents used to aid internal communication and reporting are accurate and up to date., • Ensure all logistical aspects of project delivery are communicated in a timely and accurate manner with the necessary department., • Ensure compliance and traceability opposite product integrity throughout the procurement/project supply chain., • Ensure all license documentation and QA related activities are in place and being managed opposite CT orders and project delivery., • Ensure any risks identified are escalated to the PM and Senior Director in a timely manner., • Work within current quality, regulatory and Company requirements., • Work closely with the finance team to ensure that all financial aspects of project delivery are communicated in a timely and accurate manner., • Work closely with all departments within the organization., • Understand and work within the constraints of customs, import and export regulations for global shipping and complete necessary shipping documents. Desired Candidate Profile & Capabilities Required: • Local to the St Albans area and able to travel into the office (located in Redbourn), • Bachelors or equivalent experience., • Have the right to work in the UK., • Excellent verbal and written communication skills in English., • Familiarity with project management tools, Microsoft Teams etc., • Ability to work as an individual contributor in a Results-Focused work environment., • Customer Orientation: The ability to demonstrate concern for satisfying one’s external and/or internal customers., • Problem-solving: Able to handle difficult or unexpected situations in the workplace as well as complex business challenges., • Results Orientation: The ability to focus on the desired result of one’s own or one’s unit’s work, setting challenging goals, focusing effort on the goals, and meeting or exceeding them., • Communication: Able to communicate in a clear, appropriate, effective, and efficient manner in various situations., • Project Management: Able to effectively coordinate a project from start to finish; using effective communication, interpersonal skills, and organization to complete projects within defined parameters and timelines. Compensation & Benefits • Salary £35,000 plus commission, • Pension scheme, • Private health insurance, • Attractive performance incentive plan, • Vacation, Volunteer and paid sick leave Tanner Pharma Group’s Core Values: Everything we do at Tanner Pharma Group is dictated by our values. We take them very seriously, and we're proud of this unwavering commitment. Check out view our core values and learn more about our company. Candidates may be required to organize reference calls upon request. Confidentiality will be respected. Additionally, Pre-employment drug and background screening will be required. Tanner Pharma Group is an Equal Opportunity/Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability, or protected Veteran status.

A clinical research organization in the United Kingdom is seeking an Associate Clinical Trial Manager to join their London team. Candidates will manage clinical trial activities and collaborate globally with project teams.

As a Trial Manager you will have responsibility for at least one clinical trial, including maintenance of Trial Master File and key study documentation, obtaining relevant ethical and regulatory approvals, safety reporting of adverse events, monitoring trial progress and facilitating meetings, and p

Medpace is the leading CRO for Biotech companies and is continuing to add Clinical Trial Managers of different experience levels to join our Clinical Trial Management Group in London. Clinical Trial Managers with expertise in Cardiovascular/Endocrine/Metabolic are welcome to continue to work in thei

Support the Global Clinical Trial Manager, Global Early Clinical Development Manager, Local Trial Manager, Regional or Country Study Manager in the delivery of the clinical and operational strategy and assist the execution of clinical trials. Clinical Risk Manager / Clinical Trial Manager. Senior Cl

Medpace is the leading CRO for Biotech companies and is continuing to add a Director of Clinical Trial Management (Operational role) to join our Clinical Trial Management Group in London, UK. Clinical Trial Managers with expertise in Oncology or other therapy areas are welcome to continue to work in

The Clinical Trials Manager will manage individual clinical trials and/or programs as part of the Clinical Trial Working Group. Parexel is currently seeking a Clinical Trial Manager (CTM) to join us in the UK, dedicated to a single sponsor. Working as a Clinical Trial Manager at Parexel FSP offers t

Clinical Trial Associate ManagerLocation: LondonAbout the Role**The Clinical Trial Associate Manager plays a key leadership role in ensuring the successful execution of clinical trials by overseeing a team of Clinical Trial Associates (CTAs). Clinical Trial Associate Manager page is loaded##

The aCTM will be a part of the Clinical Trial Management team working with Project Coordinators and Clinical Trial Managers in performance of clinical trial management activities. Associate Clinical Trial Manager (aCTM) to join our. Communicate and collaborate on global study activities; working clo

An educational institution in London is looking for a Trial Manager to coordinate the ‘GP‑TEST‑PRO’ cancer screening trial. The successful candidate will manage participant recruitment, oversee trial timelines, budget adherence, and ensure compliance to regulations.

The aCTM will be a part of the Clinical Trial Management team working with Project Coordinators and Clinical Trial Managers in performance of clinical trial management activities. Associate Clinical Trial Manager (aCTM) to join our Clinical Trial Management team. Communicate and collaborate on globa

Impact and Contribution: Roles within the Clinical Trial Management job family at the P22 level significantly impact the success of clinical trials by ensuring that all aspects of the study are meticulously planned and executed. Single Sponsor European Clinical Trial Manager - 2-3 days a week in Uxb

The aCTM will be a part of the Clinical Trial Management team working with Project Coordinators and Clinical Trial Managers in performance of clinical trial management activities. Associate Clinical Trial Manager (aCTM) to join our. Communicate and collaborate on global study activities; working clo

The Clinical Trial Manager is a highly autonomous and experienced clinical operations professional responsible for all aspects of Clinical Trial Management for global studies. Ensures compliance of clinical trials with national and international regulatory requirements and co‑monitors the assigned

A leading biopharmaceutical solutions organization is seeking a Clinical Trial Manager to oversee Phase III studies across Europe.

A prominent health communications agency in Greater London seeks an experienced Account Manager to oversee day-to-day client management and ensure effective delivery of projects. You'll partner with Project Managers and lead client meetings to drive success, all while enjoying fantastic benefits tha

You will work closely with project managers (central and/or specialty labs) and lend expertise to clinical trial management (CTM) and CRO to ensure samples are collected per protocol and assist with resolving any sample related issues or queries. Parexel are currently recruiting for an experienced C

A leading clinical recruitment firm in the UK is seeking a Clinical Trial Manager to lead the design and execution of global studies for the Renal Denervation portfolio. This fully remote position requires extensive experience in clinical trial operations and regulatory knowledge, as well as fluency

Finance Manager - £45k - £50k per annum - Full time - Permanent - Greater Exeter.

Single Sponsor European Clinical Trial Manager. Impact and Contribution Roles within the Clinical Trial Management job family at the P22 level significantly impact the success of clinical trials by ensuring that all aspects of the study are meticulously planned and executed. Planning logistics and r

Parexel International is seeking an experienced Clinical Trial Manager (CTM) to join their team in the UK, dedicated to managing individual clinical trials. Preferably, candidates will have experience in oncology or CNS trials.

To date, we've supported over 800 clinical trials in more than 290 conditions over 75 countries, helping to convert over 500,000 patients to a clinical trial at a time when they need it most. Webelievethat people are the most valuable asset of any clinical trial. We partner with our clients across t

A leading clinical research organization in Greater London is seeking experienced Clinical Trial Managers to oversee projects and ensure compliance with all regulations. Candidates should have at least 5 years of experience in clinical trial management, preferably within a CRO.

The Senior Manager, Clinical Trial Study Start‑Up is a subject matter expert in clinical study start‑up and is responsible for leading the process that enables planning, coordination, and execution of study, country and site‑level start‑up activities from site identification through to site

The Clinical Trial Associate Manager plays a key leadership role in ensuring the successful execution of clinical trials by overseeing a team of Clinical Trial Associates (CTAs). This position combines people leadership with operational excellence, driving consistency across clinical trial activitie

A healthcare organization in Greater London is seeking a Trial Manager for the RM-CTU Breast team. The successful candidate will coordinate clinical trials, manage documentation, and support junior staff. Responsibilities include ensuring compliance with regulatory requirements and engaging with sta

Impact and Contribution Roles within the Clinical Trial Management job family at the P22 level significantly impact the success of clinical trials by ensuring that all aspects of the study are meticulously planned and executed. Single Sponsor European Clinical Trial Manager - 2-3 days a week in Uxbr

A global biopharma company is looking for a Senior Manager, Clinical Trial Study Start-Up, to lead study start-up activities from site identification to activation.

The aCTM will work with Project Coordinators and Clinical Trial Managers in performance of clinical trial management activities. Communicate and collaborate on global study activities; working closely with the Project Coordinator and Clinical Trial Manager. Candidates should expect to have an intens

A prominent health communications agency in Greater London is seeking an Account Manager to oversee client accounts.

A leading health communications agency in Greater London is seeking an ambitious Account Manager to manage client accounts effectively.

R&D Partners is seeking a Clinical Trial Manager to lead the design, planning, execution, and oversight of global clinical studies for the Renal Denervation portfolio. Advanced knowledge of Good Clinical Practices (GCP), ISO 14155, and FDA regulations governing clinical trials. Experience with medic

A pharmaceutical company in the United Kingdom is seeking a Clinical Trial Manager to oversee all aspects of clinical trial management for global studies, ensuring compliance with regulatory standards. The ideal candidate will have a bachelor’s degree in a related field and over 5 years of experie

Together, Inclusive and TrialEngine form the only end‑to‑end platform to automate the back office of clinical trials, from pretrial to trial close. Partnerships Manager (Clinical Trial, SaaS, Health tech). Maintain strong market knowledge to spot emerging players and partnership trends in the di

A leading clinical research organization in London is seeking a Clinical Trial Manager to oversee clinical projects, primarily focusing on Nephrology. Candidates with a passion for clinical trials and at least 5 years of experience in managing such projects are encouraged to apply.

A leading biopharmaceutical company is seeking a Global Study Manager for an interim remote position. Candidates should possess a Bachelor's degree in a related field and have 3-4 years of clinical trial experience, particularly in Early Phase studies.

The Senior Clinical Trial Manager, Clinical Operations, serves as the operational lead for assigned early-phase oncology studies, providing end-to-end trial leadership from start‑up through close‑out. The senior manager has primary responsibility for international regions including Europe, Asia�

To date, we've supported over 800 clinical trials in more than 290 conditions over 75 countries, helping to convert over 500,000 patients to a clinical trial at a time when they need it most. Langland, a Publicis Health company, is the only health communications agency that thinks further across Cli

The Clinical Trial Supply Chain Manager is responsible for overseeing the supply chain and logistics of clinical trial materials to ensure timely and efficient delivery to sites across the globe. Coordinate with vendors and internal teams to ensure the timely production, packaging, labeling, and dis

We are currently looking for a Trial Vendor Senior Manager to join our team. As a Core member of the Clinical Trial Team (CTT) you will independently manage all vendor-related aspects of global clinical trial(s) to deliver study outcomes within schedule, budget, quality/compliance and performance st

To date, we've supported over 800 clinical trials in more than 290 conditions over 75 countries, helping to convert over 500,000 patients to a clinical trial at a time when they need it most. An Account Manager’s primary role is to take responsibility for the day‑to‑day management of a portfol

A leading life sciences company in London is seeking a Clinical Trial Manager to oversee the development and execution of Phase III clinical studies across Europe. The role requires strong project management and organizational skills, as well as familiarity with clinical trial management software.

The Global Study Manager is responsible for supporting the delivery of clinical studies ensuring quality and compliance. Lead the preparation of country specific agreements, confidentiality agreements, clinical trial applications and other applicable country documents. Assist in the clinical trial i

Medpace is the leading CRO for Biotech companies and is continuing to add Clinical Trial Managers of different experience levels to join our Clinical Trial Management Group in London. Clinical Trial Managers with expertise in Nephrology are welcome to continue to work in their area of expertise or t

To date, we've supported over 800 clinical trials in more than 290 conditions over 75 countries, helping to convert over 500,000 patients to a clinical trial at a time when they need it most. Langland, a Publicis Health company, is the only health communications agency that thinks further across Cli

The aCTM will be a part of the Clinical Trial Management team working with Project Coordinators and Clinical Trial Managers in performance of clinical trial management activities. Associate Clinical Trial Manager (aCTM) to join our Clinical Trial Management team. Communicate and collaborate on globa

Single Sponsor European Clinical Trial Manager - 2-3 days a week in Uxbridge. Single Sponsor European Clinical Trial Manager - 2-3 days a week in Uxbridge. Assist in training for Clinical Trials Management Associates (CTMAs) and Clinical Project Assistants (CPAs).

We are currently looking for a Trial Vendor Senior Manager to join our team. As a Core member of the Clinical Trial Team (CTT) you will independently managing all vendor-related aspects of global clinical trial(s) to deliver study outcomes within schedule, budget, quality/compliance and performance