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Thermo Fisher Scientific
3.5
Sr CTM/CTM - FSP - Germany - Atopic Dermatitis (m/w/d)
Home office
The Clinical Trial Manager is accountable for achieving the final clinical deliverable (usually clean data from evaluable patients as specified in the study……
30d+
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doinstruct Software
4.8
Senior Customer Success Manager (f/m/d)
Berlin
Our customers have real operational complexity, long internal decision cycles, and limited appetite for tools that don't immediately prove their worth.…
30d+
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Moss
3.6
Customer Support Associate (f/m/d)
Berlin
This is not a traditional support role — you will gain deep insight into our product and business while solving real customer problems.…
30d+
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Moss salaries
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Benifex
3.8
Customer Success Manager (German Speaking)
München
Growth: Build deep technical and operational expertise by supporting customer admins on a complex SaaS platform. Two days per year dedicated to volunteering.…
21d
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Aily
3.6
Sr / Principal Pharma Industry Business Impact Lead (CSM)
München
Easy Apply
This role goes beyond a traditional Customer Success Manager profile, combining strategic account leadership, executive advisory, and industry authority.…
23d
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Moss
3.6
Customer Experience Associate (f/m/d)
Berlin
This is not a traditional support role — you will gain deep insight into our product and business while solving real customer problems.…
2d
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PTC
4.1
Senior Customer Success manager
München
As a Customer Success Manager (CSM) at PTC, you will play a critical role in being responsible for post-sale account management ensuring our customers achieve……
30d+
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AstraZeneca
4.0
Country Study Manager
München
The Country Study Manager (CSM) has local responsibility for the delivery of the studies in compliance with Good Clinical Practice (GCP), and regulatory……
25d
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Deepki
4.2
Senior Sustainability Consultant - Berlin - (F/M/X)
Berlin
They will be contributing to the overall success of Deepki in the DACH market. Under the supervision of the Head of Client Delivery - Germany, your main……
30d+
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Aily
3.6
Senior / Principal Beauty & Luxury CPG Industry Business Impact Lead (CSM)
München
Easy Apply
Leverage beauty and luxury CPG industry expertise to understand business challenges translate them into AI solutions to achieve measurable business value.…
23d
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Superchat
4.8
Product Manager | Integrations (m/f/d)
Berlin
Easy Apply
You'll design API surfaces, debate OAuth and webhook patterns, and hold your own with senior engineers and external partner teams. The engineers write the code.…
22d
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DHL
3.8
Manager Project Methodology (m/f/d)
Bonn
You maintain a cohesive framework of processes, templates, standards, and quality gates while enabling teams to apply agile practices consistently and……
21d
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RoomRaccoon
2.6
Customer Success Manager (German Speaker)
Deutschland
Easy Apply
Location: Remote (DE based) or in one of our office locations (Lisbon, Breda or Cape Town) Contract Type: Full-time (12-month freelance contract, with a view to……
30d+
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ComfNet Solutions
3.7
IT- Project Manager
Hamburg
ComfNet is looking for a proficient Project Manager who is very passionate about taking up the responsibilities such as services of a project manager to manage……
30d+
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Alexion Pharmaceuticals
3.8
Country Study Manager
München
The Country Study Manager (CSM) has local responsibility for the delivery of the studies in compliance with Good Clinical Practice (GCP), and regulatory……
25d
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The Cloud People
4.6
Business Process Consultant – Customer Service ...
Stuttgart
The Cloud People is a leading Elite ServiceNow Partner, specializing in delivering innovative and scalable solutions for organizations looking to harness the……
30d+
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The Cloud People
4.6
Business Process Consultant – Customer Service Management
Leinfelden-Echterdingen
As a Business Process Consultant / Business Analyst (CSM), you ensure that business objectives, operational processes, and the ServiceNow platform remain……
30d+
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Coverflex Manufacturing
5.0
Head of Marketing - Founding Team
München
Today, thousands of companies use Coverflex to manage benefits, meal allowance, insurance, and flexible compensation through a single platform.…
30d+
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SimScale
4.8
Customer Success Manager (m/f/d)
München
Easy Apply
As a Strategic Customer Success Manager, you will be the commercial and strategic lead for a dedicated cohort of customers.…
30d+
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Moss
3.6
(Senior) Account Executive, DACH (f/m/d)
Berlin
At Moss, we give finance professionals the power to automate their day-to-day and make forward-thinking decisions. Here's a bit more of what you can expect:…
16d
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Circula
4.6
Senior Account Manager (m/w/d)
Berlin
€105K (Employer provided)
Easy Apply
Mit über 30 Nationalitäten in unseren Büros in Europa schätzen wir die Vielfalt und fördern eine inklusive Kultur, die unterschiedliche Perspektiven willkommen……
30d+
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Kayzen
4.0
Programmatic Trader (m/f/d)
Home office
Easy Apply
The Trading team is responsible for creating growth through the management and optimization of mobile performance advertising campaigns for clients utilizing……
30d+
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Netskope
4.3
Solutions Engineer
Hamburg
You will work closely with customers and partners as your primary point of contact for feedback and resolution of issues and will be the customers' advocate for……
23d
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Freshworks
3.4
Senior Account Executive - DACH (m/f/d)
Berlin
Easy Apply
Working hand-in-hand with our marketing team and our business development representatives, you will especially be responsible for the acquisition of new……
30d+
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The Cloud People
4.6
ServiceNow Senior Solution Architect
Stuttgart
You will work closely with business stakeholders to translate requirements into scalable, sustainable solutions—leveraging the ServiceNow platform to its……
30d+
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Parloa
4.6
(Senior) Technical Program Manager - Agentic AI Deployments
Berlin
Easy Apply
In this role, you'll own the end-to-end delivery lifecycle from scoping and planning through go-live and hypercare, working in a pod model alongside a Forward……
30d+
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Moss
3.6
(Senior) Account Executive, DACH (f/m/d)
München
This role will be crucial in managing the entire sales cycle, from finding a potential client to finalising the deal.…
30d+
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osapiens Services
3.4
Strategic Customer Success Manager
München
Easy Apply
Munich or Madrid · Hybrid · Full-time. The osapiens HUB serves 2,500+ customers, from Mittelstand to global enterprise, across four solution areas:……
30d+
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SimScale
4.8
Strategic Account Manager (m/f/d)
München
Easy Apply
SimScale is an engineering simulation platform that is revolutionizing the way engineers, designers, scientists, and architects design products.…
11d
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Blue Yonder
3.6
Senior Account Executive
Karlsruhe
We are looking for a Sr Account Executive with passion, high energy, Supply Chain knowledge and ideally with Grocery sales experience within the software……
30d+
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Thermo Fisher Scientific

3.5

Sr CTM/CTM - FSP - Germany - Atopic Dermatitis (m/w/d)

Home office

Is your resume a good match?

Use AI to find out how well the skills on your resume fit this job description.

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office

Job Description

Join Us as a Clinical Trial Manager/Sr Clinical Trial Manager - Make an Impact at the Forefront of Innovation
The 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.

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).

Atopic dermatitis experience as CRA and/or CTM
Ability to travel to countries within region

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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Working here doesn’t have to be a secret

3.5

Recommend to a friend
Approve of CEO
CEO: Marc N. Casper
4,722 Ratings

Thermo Fisher Scientific

3.5

Sr CTM/CTM - FSP - Germany - Atopic Dermatitis (m/w/d)

Home office

Thermo Fisher Scientific

3.5

Sr CTM/CTM - FSP - Germany - Atopic Dermatitis (m/w/d)

Home office

Is your resume a good match?

Use AI to find out how well the skills on your resume fit this job description.

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office

Job Description

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).

Atopic dermatitis experience as CRA and/or CTM
Ability to travel to countries within region

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.

See company reviews

Working here doesn’t have to be a secret

3.5

Recommend to a friend
Approve of CEO
CEO: Marc N. Casper
4,722 Ratings

Are you open to new opportunities?

38 Sr. CSM jobs in Germany

Working here doesn’t have to be a secret

Working here doesn’t have to be a secret