document review

Location: Munich, Germany Dates: 31 Aug - 4 Sep 2026 Schedule: 5 days | 4 hours per day | 9:00 AM – 1:00 PM Language: English Training Fee: 1,200 EUR (total for the full 5 days) Cambridge for Global Training is seeking a highly experienced freelance trainer to deliver an executive-level course titled Mastering Document Control in Munich. Course...

Accept a job offer: Employment Acceptance Letter The terms in your document will update based on the information you provide. Make document Accept a job offer: Employment Acceptance Letter Make document Other Names: Job Offer Acceptance Letter Job Acceptance Letter+1 more Employment Offer Acceptance Letter What is an Employment Acceptance Letter? It's...

Independently performs, coordinates and oversees all aspects of the clinical site monitoring services, assessing protocol and regulatory compliance as per Alimentiv’s and sponsor’s standard processes, ICH/GCP guidelines and local regulation. Serves as the primary liaison between the sponsor/Alimentiv and investigative sites by playing a critical role in...

Confirm a former or existing employee's salary: Salary Verification Letter The terms in your document will update based on the information you provide. Make document Confirm a former or existing employee's salary: Salary Verification Letter Make document Other Names: Income Verification Letter Wage Verification Letter+4 more Proof of Income Letter...

This position is listed on behalf of a partner company, who manages all applications and next steps. Our partner is looking for a Senior/Principal Medical Writer based in Germany. Join a specialized medical writing team supporting the development of high-quality regulatory documentation for the global pharmaceutical industry. In this role, you will...

Summary This position is located at USAG Bavaria - MWR, Tower Barracks (Grafenwoehr), Germany. Incentives and Bonuses Incentives will not be paid. This job is open to Help The public U.S. Citizens, Nationals or those who owe allegiance to the U.S. Clarification from the agency United States (U.S.) Citizens and Non-U.S. Nationals who have...

Department: Solid Waste Start Here. Grow Here. Stay Here. Do you enjoy working with your hands, operating equipment, and seeing the results of your hard work? Join Sarasota County's Solid Waste Department as a Maintenance Skilled Trades Worker II, where you'll perform a variety of maintenance, repair, and improvement projects that help keep our facilities...

Your Tasks:   Operational responsibility for incoming loan applications Review of financing documents, followed by approval, authorisation and comments Identification of credit risks based on specific creditworthiness checks, analysis of balance sheets and financial reports, and requests for further financing documents Clarification of...

The RoleAccounting Preparation of annual financial statements Responsibility for the completion of annual financial statements Main point of contact for external auditors General accounting activities Recording and processing accounting documents in the accounting software Posting credit card statements and preparing travel expense reports Tax Preparation of...

Responsible for the clinical operations of a project within a defined regional/global level. Provides oversight of project deliverables, assigned Clinical Research Associate (CRAs) and Investigator sites in accordance with the Monitoring Plan, Protocol, Good Clinical Practice (GCP), ICH guidelines and local regulations. The COL acts as a primary liaison...

We are looking for fluent German speakers to label information in documents to support the development of data security systems. This is a perfect opportunity for students, beginners, and anyone looking to gain experience in the digital and AI sectors. Responsibilities * Review documents and identify personally identifiable information, including ...

Responsible for the clinical operations of a project within a defined regional/global level. Provides oversight of project deliverables, assigned Clinical Research Associate (CRAs) and Investigator sites in accordance with the Monitoring Plan, Protocol, Good Clinical Practice (GCP), ICH guidelines and local regulations. The COL acts as a primary liaison...

Responsible for the clinical operations of a project within a defined regional/global level. Provides oversight of project deliverables, assigned Clinical Research Associate (CRAs) and Investigator sites in accordance with the Monitoring Plan, Protocol, Good Clinical Practice (GCP), ICH guidelines and local regulations. The COL acts as a primary liaison...

Seeking Experienced Project Engineer With Great Attitude Our Company – Cascade Built – Seattle, WA Mid-size, established and growing strategically Urban construction and real estate development Builds and develops in Seattle’s urban neighborhoods building cutting edge, high-performance sustainable/green projects ranging from single-family to...

ARIS is a Process Intelligence company that helps organizations discover, create, and transform their processes to deliver measurable business outcomes and scale AI with confidence. It combines process design, real execution insight, and AI-driven optimization in a single, integrated platform-enabling organizations to build a governed digital twin of their...

We are seeking a Hepatologist to join our team in Munich. The Medical Director will have overall responsibility for providing medical, scientific, and strategic leadership for the successful planning, execution, and reporting of clinical trials. Additionally, this role acts as the Medpace internal medical expert and will serve as a medical resource for the...

Location: Hybrid / Munich Hours: ~20h/week (working student status) Start: ASAP ABOUT THE ROLE We build AI solutions for engineering. Our platform turns documents, technical drawings and CAD data into structured knowledge for engineers. You will work on the full stack: frontend, backend APIs, worker pipelines and deployment. WHAT YOU'LL WORK ON •...

We are looking for fluent German speakers to label information in documents to support the development of data security systems. This is a perfect opportunity for students, beginners, and anyone looking to gain experience in the digital and AI sectors. Responsibilities Review documents and identify personally identifiable...

The Clinical Research Associate II is responsible for the feasibility, initiation, monitoring, and close-out of investigative sites. Major responsibilities include ensuring the safety and well-being of study participants at assigned sites, ensuring site compliance with Good Clinical Practice (GCPs), applicable regulations, the protocol and study plans;...