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Study Coordinator

vor 5 Monaten

Munich, Deutschland Linical Europe Vollzeit

**Linical Co.**, Ltd. (‘Linical’) is a premier global CRO headquartered in Osaka, Japan, listed in the prime segment of the Tokyo Stock exchange, and dedicated to serve its clients as a true partner in development. With approximately 900 employees Linical directly covers a total of more than 20 countries in Europe, North America and Asia-Pacific including Japan via its own offices and staff.

Linical’s European arm is headquartered in Frankfurt, Germany with a substantial presence in Paris and Madrid. Its geographic footprint facilitates a significant presence in the leading Western European markets, combined with well-established affiliate operations in key emerging markets in Central
- and Eastern Europe.

We offer individualized solutions that are tailored to the specific needs of our sponsors. We work as integrated teams functioning with maximum transparency throughout each study, making sure that the sponsor is kept up to date on all study parameters and progress. We are dedicated to the highest standards of quality, with a special focus on the therapeutic areas oncology, immunology and CNS, based on experience and expertise.

**Pharma Resourcing Solutions PRS**

Linical Pharma Resourcing Solutions (Linical PRS) has the experience and a clear understanding of the importance of our clients’ resourcing strategies. With the flexibility that this level of service requires, Linical is able to serve a full range of resourcing requirements as per our clients’ needs and expectations.

Linical PRS is supported by a strong and continuous recruitment activity, accompanied by qualified and highly experienced line management personnel as well as strong leadership oversight throughout the process. Thus, PRS can guarantee success and commitment to the project objectives of our clients.

We truly believe people are the real value of a company and we invest in their performance and their professional satisfaction.

**Responsibilities**:

- Set-up and maintain project files (electronic and hardcopy) and project plan
- Coordinate tests and procedures of clinical trial participants.
- Support CRAs in charge of the follow up of the clinical trial and solve any problem that may arise during the different phases of the clinical trial.
- Queries resolution
- Maintain time lines of the studies
- Data collection as it is specified in the protocol and assure the timely termination of CRFs (Case Report Forms).
- Have a fluent communication with the Sponsor, clinical trial participants and the IP during the development of the study.
- Support and follow-up for audit and quality assurance activities.
- Ensure study information and documents are maintained following guidelines and in the appropriate systems.
- Correct distribution of materials.
- Administrative responsabilities.