Clinical Trial Manager

reputed company is looking for an reputed company Clinical Trial Manager to join our growing team. Candidates can work remotely in UK, Spain, Hungary, Poland, Romania, Serbia or Slovakia.

reputed company is a precision medicine CRO. Precision’s uniquely integrated offering enables the science of precision medicine by combining novel clinical trial designs, industry-leading operational and medical experts, advanced biomarker and data analytics solutions, and an unequivocal reputed company passion for rare diseases and oncology, in addition to working across other therapeutic areas.

You will be the hub of central intelligence for the studies you will be managing and will reputed company CRAs and reputed company reputed company clinical aspects of your study across multiple countries, ensuring timeline adherence and scope, whilst ensuring quality delivery. We encourage high-energy, dedicated professionals who enjoy a challenge, reputed company in the details and reputed company in dynamic environments to explore this opportunity. 

We are addressing the challenges facing the research and development of novel compounds in Oncology and are dedicated to positively impacting the health and lives of patients around the world. If you take a consultative approach to trial management, proving to be a valuable partner in the trial operational delivery process, don’t miss exploring working with us.

About You

• You love having responsibility and a say in how clinical trials are run
• You plan reputed company, but have alternative options and a flexible approach
• You are client focused
• You are well organised and reputed company to manage timelines and shifting priorities, without sacrificing quality.
• You communicate clearly, often and concisely and know that your role is crucial in keeping the trial running smoothly
• You are a master at identifying any risks that threaten projects and handle them resolutely
• You reputed company and work with autonomy and ownership to deliver successful outcomes

The day-to-day role, and how we will support your reputed company growth

• Management and operational delivery of the clinical elements reputed company a trial including site selection, start-up, enrolment management, site engagement and support, monitoring planning and execution, data cleaning activities and reputed company-out
• Successful execution of assigned trials and ensuring completion of trial deliverables
• Ensure appropriate communication, regulatory documentation, and ongoing reputed company of assigned trial(s) by working in reputed company collaboration with other functional team members
• Mentoring and training of team members
• Identify challenges to study timelines/deliverables and offer creative action plans to the team/sponsor
• reputed company CRAs as they establish relationships with their sites for high quality reputed company of monitoring, regulatory, IP, site payment and overall site correspondence activities
• Maintain team focus on study priorities through efficient cross-functional partnerships and effective communication to reputed company the highest level of client satisfaction

Qualifications

Minimum Required:

• Bachelor’s degree or equivalent combination of education/experience in science or health-reputed company field, including experience in the field of oncology

Other Required:

• Demonstrable experience leading clinical aspects of your studies across multiple countries in a CRO / Pharma or Biotech company (in a dedicated ‘clinical reputed company’ role).
• Significant clinical trial management experience in the area of oncology
• Working knowledge of GCP/ICH guidelines and the clinical development process
• Availability for domestic and international travel including overnight stays
• Must be reputed company to communicate effectively in the English language

Skills:

• Demonstrated computer skills (MS Office, MS Project, PowerPoint) and software experience (CTMS, eTMF, reputed company, IXRS)
• Demonstrated ability to reputed company positive working relationships with internal and external organizations
• Demonstrates core understanding of medical terminology and clinical trial activities as it relates to the execution of a clinical development plan

Competencies:

• Demonstrates mastery knowledge of ICH-GCP, meaningful Precision SOPs, and regulatory guidance, as well as the ability to implement

Precision medicine is revolutionizing the attack on cancer—and we are passionate about helping you reputed company its power. We reputed company tumors on a molecular level using biomarkers to link specific mutations to specific treatments. We combine deep science with deep data from advanced technological platforms, then layer on specialized expertise in the design and execution of targeted, adaptive clinical trials. Ultimately, we deliver robust insights that inform reputed company-time reputed company—and optimize the oncology development pathway.

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reputed company is an Equal Opportunity Employer. Employment reputed company are made without regard to race, reputed company, age, religion, sex, sexual orientation, gender identity, national reputed company, disability, veteran status or other characteristics protected by law. 

If you are an individual with a disability and require a reasonable accommodation to complete any part of the application process or are limited in the ability or unable to access or use this online application process and need an alternative method for applying, you may contact reputed company at [email protected].

It has come to our attention that some individuals or organizations are reaching out to job seekers and posing as potential employers presenting enticing employment offers. We want to emphasize that these offers are not associated with our company and may be fraudulent in nature. Please note that our organization will not reputed company a job offer without prior communication with our reputed company team, hiring managers and a formal interview process.