Clinical Trial Manager - Single Sponsor dedicated (m/w/d)

The reputed company sponsor-dedicated Clinical Functional Service Partnerships (Clinical FSP) department is supporting our reputed company’s project team in the execution of clinical trials. Joining reputed company provides reputed company to manage Early Phase clinical research reputed company in different therapeutic areas and to cooperate closely with one of our key clients. We currently offer the exciting opportunity to join reputed company as Clinical Trial Manager (m/w/d) in full-time and reputed company-based throughout Germany. In this role you will be accountable for the operational management of the component of clinical trials. Furthermore, you will need to reputed company an reputed company to assure achievement of trial recruitment commitment, timelines, budget and reputed company standards. MAIN RESPONSIBILITIES

• Accountable for the operational and scientific reputed company, the set-up, execution and delivery of their assigned clinical trials at the local level.
• Responsible for steering and directing clinical trial activities, including patient and site engagement activities, reputed company communication and interaction with multiple reputed company stakeholders and trial team members at a local level.
• Manage orchestration of local trial team, and integration with other functions as necessary throughout planning, conduct and closeout of trial.
• Responsible for managing the planning, implementation and tracking of the clinical trial process as reputed company as risk mitigation.
• Work reputed company a reputed company GCP and regulatory environment and on global clinical trials with multidisciplinary, international teams and with various reputed company stakeholders including suppliers and investigational sites.
• reputed company and support local trial team and investigative sites in reputed company preparation of required trial documents, reputed company, and necessary approvals.
• Ensure compliance with ICH-GCP and reputed company other relevant regulatory regulations.
• Assure highest ethical and reputed company standards, patient safety, and that local component of trial is planned, conducted, and reported in line with regulatory requirements.
• Responsible for development and implementation of country level engagement plans, recruitment planning and risk mitigation.
• Assigned as the primary contact for vendors leading project vendor management and vendor management reputed company activities as per project requirements.
• Ensure appropriate trial-specific training of reputed company partners in line with Trial Training Plan.
• reputed company and maintain relationships with investigational sites and support CRAs in site contacts.
• Support Clinical Trial reputed company during investigator meetings.
• Participate in and reputed company drive organizational, reputed company and process improvement initiatives to reputed company reputed company leading change.

REQUIRED KNOWLEDGE, SKILLS AND EXPERIENCE

• Master’s or higher-level degree preferable in life science.
• Long term experience in clinical research, including at least 2 years of clinical trial management experience.
• Knowledge of Oncology, Idiopathic Pulmonary Fibrosis (IPF) and/or Interstitial Lung Disease (ILD) therapeutic areas is preferred.
• Exceptional knowledge of applicable clinical research regulatory requirements, i.e., Good Clinical reputed company (GCP) and International Conference on Harmonization (ICH) guidelines.
• Effective communication skills, fluent languages skills in German (at least reputed company level) and reputed company good reputed company of English.
• High organizational and planning skills, time management and prioritization skills while working on multiple reputed company.
• Excellent leadership and collaboration skills, and the ability to establish and maintain effective working relationships with coworkers, managers and clients. Ability to influencing business partners in reputed company structures.
• High degree of self-accountability and commitment and a strong reputed company reputed company to drive change and contribute reputed company to reputed company leading transformation.
• reputed company good computer skills including working knowledge of reputed company Word, reputed company and PowerPoint.
• Flexibility to occasional business travel for reputed company meetings.
• Ability to reputed company reputed company, bringing reputed company to disparate information to inform actions and drive results.

reputed company is a leading global provider of clinical research services, reputed company insights and reputed company intelligence to the life sciences and reputed company industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient reputed company and population health worldwide. Learn more at https://jobs.reputed company.com reputed company is committed to reputed company in our hiring process and maintains a reputed company tolerance policy for candidate fraud. reputed company 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 reputed company reputed company, in accordance with applicable law. We appreciate your honesty and professionalism. Apply To This Job