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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.

Minimum 5 years' experience in longitudinal clinical research, including hands‑on clinical trial experience (industry or academic setting). Partner closely with cross‑functional teams including Clinical Operations, Safety, Biostatistics, Regulatory Affairs, Clinical Pharmacology, Biomarkers, and

A global biotechnology company seeks a Lead Medical Director in Welwyn to oversee the Clinical Development Plan for designated drugs. The ideal candidate will have over 5 years of clinical trial experience, proficiency in gastroenterology or hepatology, and a deep understanding of Phase II/III drug

FDA, EMA)* You have a strong understanding of statistical principles and methodology relevant to clinical trial design and analysis* You are proficient in SAS and/or R and familiar with CDISC standards* You demonstrate capacity for independent thinking and ability to make decisions based upon sound

A leading pharmaceutical company based in Welwyn seeks a Medical Director in Ophthalmology.You will lead clinical strategies from pre-clinical stages and ensure trial compliance and ethical standards.Ophthalmology and a proven track record in the pharmaceutical industry.This role involves significan

For many, taking part in clinical research offers hope, purpose, and a chance to shape the future of dementia care. But finding the right trial, understanding what it involves, and knowing how to take part can be confusing.

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.

A global healthcare innovator is looking for a Senior Statistician to provide statistical expertise in the design, conduct, analysis, and interpretation of clinical trials. The role requires a master's or doctoral degree in Statistics or a related field and at least three years of relevant experienc

Minimum of 3‑4 years of progressive clinical trial experience. Lead the preparation of country specific agreements, confidentiality agreements, clinical trial applications and other applicable country documents. Assist in the clinical trial insurance process; track approvals, revisions and renewal

Want to join a fast‑paced, exciting department working with some of the biggest names in healthcare? At Langland CTE (Clinical Trial Experience), we create campaigns that recruit and support volunteers for groundbreaking clinical trials. To date, we've supported over 800 clinical trials in more th

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.

A leading health communications agency in Greater London seeks an experienced Account Manager to oversee campaigns for clinical trial recruitment.

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. All materials we create are translated and rolled‑out in each country supporting the clinical trial. Langl

A leading healthcare communications agency is seeking an experienced Account Manager to oversee client services in clinical trial campaigns.

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. All materials we create are translated and rolled‑out in each country supporting the clinical trial. Langl

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. Want to join a fast-paced, exciting department working with some of the biggest names in healthcare? At Lang

In this role, you will create impactful campaigns for clinical trials, manage vital client relationships, and ensure the success of global health initiatives.

Job Description:**Job Title:Director, Clinical Trial Management SystemsDivision / Function:Clinical Trial Excellence, Clinical Development OperationsManager’s Job Title:Head of Clinical Trial ExcellenceLocation:London, UK - Paris, France - Cambridge, USWHAT - **Summary & Purpos

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

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. Work with the clinical trial management staff to support

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.

A clinical trial consultancy in the United Kingdom is looking for a skilled statistical lead to oversee clinical trial programs/projects. Master’s degree in statistical science or a related field, along with demonstrated experience in clinical trial projects. You will provide statistical methodolo

Want to join a fast‑paced, exciting department working with some of the biggest names in healthcare? At Langland CTE (Clinical Trial Experience), we create campaigns that recruit and support volunteers for groundbreaking clinical trials. To date, we've supported over 800 clinical trials in more th

The Clinical Trials Manager will manage individual clinical trials and/or programs as part of the Clinical Trial Working Group. Manage monitoring activities (may include routine on-site clinical monitoring) at clinical study sites to assure adherence to Good Clinical Practices (GCPs), SOPs and study

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

A leading dermatology company based in London is seeking a Clinical Trial Associate Manager to ensure successful execution of clinical trials. The role involves overseeing a team of Clinical Trial Associates, ensuring compliance with ICH-GCP and regulatory requirements. Candidates should possess a B

A leading biopharmaceutical solutions organization is looking for a Single Sponsor European Clinical Trial Manager to coordinate Phase III clinical research studies across Europe. The successful candidate will have a bachelor's degree in life sciences or clinical research and experience in managing

A leading clinical research organization based in London is seeking an Associate Clinical Trial Manager to join their team. The position includes a comprehensive training period aimed at enhancing your career in clinical research and development. This full-time role offers a dynamic work environment

A leading healthcare communications agency in Greater London is seeking an Account Manager to oversee the management of key client accounts.This position demands excellent verbal and written communication skills, ability to manage multiple projects, and a passion for healthcare.The ideal candidate w

This full-time, office-based role involves implementing recruitment strategies for clinical research trials, collaborating with Clinical Research Associates, and ensuring effective patient retention. A leading clinical research organization is seeking a Sr Clinical Patient Recruitment Coordinator to

Assist in training Clinical Trials Management Associates (CTMAs) and Clinical Project Assistants (CPAs). Proficiency with clinical trial management software and tools. As a P22 level Clinical Trial Manager, you will oversee the development, coordination, and implementation of Phase I‑IV studies, e

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. Compile and maintain project-specifi

This role involves leading statistical input into clinical trials and collaborating with cross-functional teams. The ideal candidate will hold an MSc or PhD in a quantitative field, possess proven experience in clinical trial statistics, and be proficient in SAS and R.

Vice President, Global Clinical Trial Management. This has been driven by the successful delivery of clinical trials of the highest standards, through their people, innovation and transparency. VP Global Clinical Trial Management.

Associate Clinical Trial Manager (aCTM). Clinical Trial Management team. Clinical Trial Management (CTM).

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

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. All materials we create are translated and rolled‑out in each country supporting the clinical trial. Langl

Responsibilities will include: education of patients, families, and colleagues; coordination of the care of patients on trials; collection and preparation of biological samples; collection of trial data; monitoring of expected and unexpected side effects of drugs and other treatment modalities; deve

Senior Sales Representative/ BDM – Clinical Trial Services. Outsourced scientific or operational services supporting clinical trials. This role is responsible for generating new business and developing existing client relationships across biotechnology and pharmaceutical organisations involved in

Provides guidance to clinical teams and clinical sites regarding collection, storage, and shipping of samples acquired in the course of clinical trials or other human sample acquisition projects. We are seeking a professional with working knowledge of clinical trials and clinical databases. Prior ex

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. Want to join a fast-paced, exciting department working with some of the biggest names in healthcare? At Lang

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. Assist in training for Clinical Trials Management Associates (CTMAs) and

Parexel International is seeking an experienced Clinical Trial Manager (CTM) to join their team in the UK, dedicated to managing individual clinical trials. Candidates should have at least 5 years of experience in clinical studies and a Bachelor's or nursing degree. Preferably, candidates will have

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

A leading health communications agency is seeking an experienced Account Manager to join their Clinical Trial Experience team. The role involves creating impactful campaigns for clinical trials and managing relationships with pharmaceutical clients.

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. Want to join a fast‑paced, exciting department working with some of the biggest names in healthcare? At La

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