18 publicaciones de empleo destacadas en cell development (¡Están contratando!)

Senior/Principal Clinical Team Manager, Hematology/Oncology
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Senior Project Manager (MCF/ Data Centres)
Royal HaskoningDHV —Málaga, Málaga provincia
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- Inglés
- Oficina
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Head of BESS, Global
Enfinity Global —Madrid, Madrid provincia
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- Máster
- Grado
- Ingeniería eléctrica
- Vacaciones pagadas
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Senior Analog Designer
Analog Devices —Valencia, Valencia provincia
- Jornada completa
Architectural/ Civil/ Structural BIM Modeler (MCF/ Data Centres)
Royal HaskoningDHV —Málaga, Málaga provincia
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Lead Mechanical Engineer (MCF/ Data Centres)
Royal HaskoningDHV —Málaga, Málaga provincia
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- Español
- Inglés
- Oficina
Lead Structural Engineer (MCF/ Data Centres)
Royal HaskoningDHV —Málaga, Málaga provincia
- Jornada completa
- Español
- Inglés
- Máster
Staff Engineer, Physical Design
Analog Devices —Valencia, Valencia provincia
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- Oficina
- Scripting
Electrical/ Mechanical BIM Modeler (MCF/ Data Centres)
Royal HaskoningDHV —Málaga, Málaga provincia
- Jornada completa
- Español
- Inglés
- Oficina
Associate Director, Brand Marketing (m/f/x) – Berinert/Haegarda
CSL Behring —Barcelona, Barcelona provincia
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- CRM software
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Senior Fullstack Engineer - Accounting - 100% Remote - EMEA
Hostaway —Barcelona, Barcelona provincia
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Design Manager (MCF/ Data Centres)
Royal HaskoningDHV —Málaga, Málaga provincia
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- Oficina
Associate Director, Medical Affairs
Vertex Pharmaceuticals —Madrid, Madrid provincia
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Data Manager (Childhood cancer and blood disorders)
VHIR —Barcelona, Barcelona provincia
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3d
OPEN CALL FOR PREDOCTORAL FELLOWSHIP- FPU/ FI-AGAUR Joan Oró
IGTP —Badalona, Barcelona provincia
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- Doctorado
- Hospital
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Sr Software Engineer - Media Buying Team
Channel Factory —España
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Senior/Principal Clinical Team Manager, Hematology/Oncology

Thermo Fisher Scientific -
En remoto

Solicitar ahora

Detalles del empleo

Jornada completa

Cualificaciones

Microsoft Word
Microsoft Excel
Inglés
Máster
Grado
Estimación y pronóstico
Liderazgo
Habilidades de comunicación

Descripción completa del empleo

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office

Job Description

Join us as a Senior Clinical Trial Manager - Make an Impact at the Forefront of Innovation

The Senior Clinical Trial Manager is accountable for achieving the final clinical deliverable (usually clean data from evaluable patients as specified in the study protocol) within the time period specified in the contract with the customer. The Clinical Trial Manager interprets data on project issues and makes good business decisions with support from experienced team members or line manager. Works to ensure that all clinical deliverables meet the customer's time/quality/cost expectations. Maintains profitability by ensuring clinical activity is conducted within contract scope, through efficient management of the clinical team. The position involves working on projects of low to moderate complexity and as part of a team of CTMs.

We are seeking experienced Clinical Trial Managers (CTMs) to join our growing Hematology/Oncology team. Ideal candidates will bring regional and/or global CTM experience, along with expertise in one or more of the following therapeutic areas and indications:

Ovarian Cancer
Sickle Cell Disease
Non-Hodgkin Lymphoma
Acute Myeloid Leukemia (AML)
Glioma
Head & Neck Cancer
Pancreatic Cancer
Prostate Cancer
Non-Small Cell Lung Cancer (NSCLC)
Breast Cancer
Colorectal Cancer

Experience with Radiopharmaceuticals, Cell & Gene Therapy, and CAR-T therapies is highly desirable.

What You'll Do:

Manage all clinical operational and quality aspects of allocated studies, of low to moderate complexity, in compliance with ICH GCP. In accordance to project specific requirements, may assume Clinical Study Manager (CSM) responsibilities on small and/or less complex projects.
Develop clinical tools (e.g. Monitoring Plan, Monitoring Guidelines) in conjunction with the Data Quality Plan. Contribute to the development of the Master Action Plan (MAP) for providing clinical related documents. Ensure timely set up, organization, content and quality of the relevant sections of the Trial Master File (local and central). May participate in the design and development of CRFs, CRF guidelines, patient informed consent templates and other protocol specific documents as required. Collaborate with the project manager to prepare, organize, and present at client meetings, including bid defense and hand-off meetings.
Collaborate with the clinical team and other departments as needed to meet deliverables of the project. Regularly communicate with the team and lead team meetings to ensure that timelines, resources, interactions, and quality are maintained. Responsible for the implementation and training of standardized clinical monitoring processes within the study and according to corporate standard policies. Responsible for the timely archiving of documents and study materials for the department.
Ensure achievement of the final clinical deliverable within the contractual time period specified by preparing and monitoring clinical activity timelines and metrics, providing status updates to the project manager, regularly reviewing projects using tracking and management tools, implementing recovery actions, reviewing monitoring visit reports, and managing CRF collection and query resolution. Continuously monitor or co-monitors clinical trials to assess performance and ensure contractual obligations are met. In smaller regions, may routinely conduct Accompanied Field Visits (AFVs) and be accountable for project financials.
May communicate with study sites regarding issues such as protocol, patient participation, case report form completion and other study-related issues.
May coordinate all start-up activities and ensures that timely ethics committee and regulatory submissions (if appropriate) are addressed. Ensure that essential document quality meets the expectation of Regulatory Compliance Review. Review and follows up on all questions raised by the ethics committees.
May provide input into preparation of forecast estimates for clinical activities. Responsible for clinical resource management, assignment, delegation of clinical responsibilities and identification of additional resource requirements.

Education & Experience Requirements:

Bachelor's degree or equivalent and relevant formal academic / vocational qualification
Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 5+ years).

In some cases an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role.

Knowledge, Skills, Abilities:

Good leadership skills, effective at mentoring and training, and capable of motivating and integrating teams
Good planning and organizational skills to enable effective prioritization of workload
Solid interpersonal and problem solving skills to enable working in a multicultural matrix organization
Capable of working effectively in a changing environment with complex/ambiguous situations
Familiarity with the practices, processes, and requirements of clinical monitoring
Good judgment and decision making skills
Effective oral and written communication skills, including English language proficiency
Capable of evaluating workload against project budget and adjusting resources accordingly
Sound financial acument and knowledge of budgeting, forecasting and fiscal management
Strong attention to detail
Solid understanding of relevant regulations e.g. ICH/GCP, FDA guidelines, etc.
Good computer skills to effectively use automated systems and computerized applications such as Outlook, Excel, Word, etc.

Working Conditions and Environment:

Work is performed in an office environment with exposure to electrical office equipment.
Frequently drives to site locations and frequently travels both domestic and international.

Why Join Us?

When you join Thermo Fisher Scientific, you become part of a global team that values passion, innovation, and a commitment to scientific excellence. You’ll work in an environment where collaboration and development are part of the everyday experience—and where your contributions truly make a difference.

Apply today to help us deliver tomorrow’s breakthroughs.

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