There is a new Thermo Fisher Scientific is currently advertising a new job opportunity. This is a full time home based role.
Key Responsibilities:
- Provides trial status tracking and progress update reports to the Clinical Team
- Manager (CTM) as required. Ensures study systems are updated per agreed study conventions (e.g. Clinical Trial Management System, CTMS). Performs QC check of reports generated from CTMS system where required.
- Participates in investigator meetings as vital. Identifies potential investigators in collaboration with the client company to ensure the acceptability of qualified investigative sites. Initiates clinical trial sites according to the relevant procedures to ensure compliance with the protocol and regulatory and ICH GCP obligations, making recommendations where warranted. Ensures trial close out and retrieval of trial materials.
- Ensures that required crucial documents are complete and in place, according to ICH-GCP and applicable regulations.
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Keys To Success For The Job Opening At Thermo Fisher
Education and Experience:
Bachelor’s degree in a life sciences related field or a Registered Nursing certification or equivalent and relevant formal academic / vocational qualification.
Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 2+ years as a clinical research monitor).
Knowledge, Skills and Abilities:
- Effective clinical monitoring skills.
- Demonstrated understanding of medical/therapeutic area knowledge and medical terminology.
- Excellent understanding and demonstrated application of ICH GCPs, applicable regulations and procedural documents.
- Ability to work in a team or independently as required.
- Good digital literacy: proficient knowledge of Microsoft Office and the ability to learn appropriate software.
- Good English language and grammar skills.
- Good presentation skills.
How To Apply
