Publicat 01 Iul 2019 | Reactualizat 31 Iul 2019 | Expiră 01 Aug 2019

Clinical Research Coordinator

1 post
Expirat
Anunț inactiv

Acest anunț a expirat și nu este disponibil pentru aplicare.

Înapoi la joburi

Candidatul ideal

Job Requirements

Education: Master degree, preferable – Medical or Biological; at least 2 years experiences as a Clinical Research Assistant related experience preferred or similar role;
Must possess excellent organizational an interpersonal skills.
Language Ability: English – communicative, other languages
preferable.
Ability to read and interpret documents, write routine reports and
Correspondence.
Math Ability: ability to calculate figures and amounts such as
discounts, interest, commissions, proportions, percentages,
circumference, and volume. Ability to apply concepts of basic algebra and geometry.
Reasoning Ability: Ability to apply common sense understanding to carry out instruction furnished in written, oral, or diagram form. Ability to deal with problems involving several concrete variables in
standardized situations.
Computer skills: To perform this job successfully, an individual
should have a ‘better than’ working knowledge of Microsoft Office
applications including MS Word, Excel, and PowerPoint.

Descrierea jobului

Summary of the job
To provide technical support for planning, conducting and
documenting all project – related activities within office and/or laboratory parts of the department.
Archiving all project-related documents.
Responsible for working in accordance to actual regulatory guidelines and internal SOPs.

Job description

Performs other related duties and tasks as necessary or as assigned;
Training of new CRC and/or CRA employee
Supervising CRA activities;
Activities using SOP forms;
Preparing archiving documents;
To provide support for the APM functions if needs;
To prepare the Laboratory Manual for the project;
To approve the laboratory results report (formal and essential approval);
To contact with investigator;
Preparing/Formal checking of project reference values list;
Participation to SIVs if asked;
Data cleaning;
Documents archiving;
To assist the APM in the coordination of supplies for each clinical study;
To coordinate all logical aspects of the project;
Arranging transport of specimens related to clinical trials;
Arranging transport of frozen shippers and specimens;
Perform materials/shipment packages quality assessment;
Sampling kit design;
Solving queries from clients related to laboratory aspects of the project;
Solving queries from clients related to logistics aspects of the project;
Perform sample quality assessment;
To coordinate all laboratory activities regarding the project;
Calibration and maintenance of SCL equipments according to calibration and maintenance plan;
Registration the samples into LIS/CTLMS;
Maintaining and developing study related relationships with subcontracted labs and vendors;
Ensure that all laboratory results will be sent of properly;

Descrierea companiei

Synevo este liderul în diagnostic de laborator în România și are în portofoliu peste 2000 de teste de bază și avansate, pentru toate ariile terapeutice efectuând în anul 2018 peste 98 milioane de teste. La finalul anului 2018 Synevo România administrează o rețea națională de 16 laboratoare și 99 de centre de recoltare a probelor biologice. Synevo România face parte din Medicover – unul dintre cei mai importanți furnizori internaționali de servicii medicale și de diagnostic, înființat în 1995 (www.medicover.com).

Pentru mai multe informații, vizitați www.synevo.ro.

Expirat
Clinical Research Coordinator  -  SYNEVO ROMANIA

E timpul pentru un browser mai bun

De la 1 octombrie 2019, te informăm că site-ul eJobs.ro nu va mai putea fi accesat prin browser-ul Internet Explorer din cauza funcționalităților reduse ale acestuia. Accesează-ne cu încredere folosind unul dintre browserele mai moderne: Google Chrome, Mozilla Firefox, Safari sau Edge.

Am înțeles
close