Lavori attuali relativi a Research Associate - Desio MB - OPIS
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Clinical Research Associate: Drive Study Success
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Desio (MB), Italia OPIS A tempo pienoA leading biotech CRO in Italy is seeking a Clinical Research Associate (CRA) to coordinate clinical studies and ensure compliance with protocols. The ideal candidate will possess a degree in a scientific field, preferably with some experience in clinical research. Responsibilities include conducting feasibility studies, monitoring sites, and ensuring data...
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Research Associate
19 minuti fa
Desio (MB), Italia OPIS A tempo pienoClinical Research Associate (CRA) Clinical Research Associate (CRA) is responsible for coordinating and overseeing the execution of clinical studies, mainly observational, and clinical investigations under the supervision by the Project Manager: identify, select, initiate and close‐out appropriate investigational sites for clinical studies and clinical...
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Clinical Research Associate: Study Monitor
7 giorni fa
Desio (MB), Italia OPIS s.r.l. A tempo pienoA biotech-focused CRO in Italy is seeking a Clinical Research Associate (CRA) to coordinate and oversee clinical studies, ensuring compliance with protocols and regulations. The ideal candidate should have a degree in a scientific field and up to 12 months of experience as a CRA. Responsibilities include site monitoring, interaction with regulatory teams,...
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Clinical Research Associate
19 minuti fa
Desio (MB), Italia OPIS A tempo pienoClinical Research Associate (CRA) Clinical Research Associate (CRA) is responsible for coordinating and overseeing the execution of clinical studies, mainly observational, and clinical investigations under the supervision by the Project Manager: identify, select, initiate and close‐out appropriate investigational sites for clinical studies and clinical...
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Desio (MB), Italia Successinjapan A tempo pienoA leading international Clinical Research Organization is seeking a Business Development Associate to expand its global network within the life sciences sector. The role requires fluent English and Japanese, with responsibilities including conducting market research, contacting clients, and maintaining CRM data. OPIS offers competitive salary, training, and...
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Clinical Research Associate: Study Monitor
2 giorni fa
desio, Italia OPIS s.r.l. A tempo pienoA biotech-focused CRO in Italy is seeking a Clinical Research Associate (CRA) to coordinate and oversee clinical studies, ensuring compliance with protocols and regulations. The ideal candidate should have a degree in a scientific field and up to 12 months of experience as a CRA. Responsibilities include site monitoring, interaction with regulatory teams,...
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Clinical Research Associate: Study Monitor
4 giorni fa
Desio, Italia OPIS s.r.l. A tempo pienoA biotech-focused CRO in Italy is seeking a Clinical Research Associate (CRA) to coordinate and oversee clinical studies, ensuring compliance with protocols and regulations. The ideal candidate should have a degree in a scientific field and up to 12 months of experience as a CRA. Responsibilities include site monitoring, interaction with regulatory teams,...
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Clinical research associate
5 giorni fa
Desio (MB), Italia OPIS A tempo pienoClinical Research Associate (CRA) is responsible for coordinating and overseeing the execution of clinical studies, mainly observational, and clinical investigations under the supervision by the Project Manager: identify, select, initiate and close-out appropriate investigational sites for clinical studies and clinical investigations. To monitor those sites...
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Clinical Research Associate
4 settimane fa
Desio (MB), Italia OPIS A tempo pienoClinical Research Associate (CRA) is responsible for coordinating and overseeing the execution of clinical studies, mainly observational, and clinical investigations under the supervision by the Project Manager: identify, select, initiate and close-out appropriate investigational sites for clinical studies and clinical investigations. To monitor those sites...
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Clinical Research Associate
7 giorni fa
Desio (MB), Italia OPIS s.r.l. A tempo pienoClinical Research Associate (CRA) is responsible for coordinating and overseeing the execution of clinical studies, mainly observational, and clinical investigations under the supervision by the Project Manager: identify, select, initiate and close-out appropriate investigational sites for clinical studies and clinical investigations. To monitor those sites...
Research Associate
4 settimane fa
Clinical Research Associate (CRA) is responsible for coordinating and overseeing the execution of clinical studies, mainly observational, and clinical investigations under the supervision by the Project
Manager: identify, select, initiate and close-out appropriate investigational sites for clinical studies
and clinical investigations. To monitor those sites to ensure that studies are carried out according to
Participate in the feasibility process of new studies/clinical investigations, collect feasibility questionnaire (if applicable) and other documents necessary for the ethical and administrative
verify that the Investigator and staff are qualified for the study and have sufficient available time and resources/facilities; verify that the Site is suitable with regard to its structure, instruments and the availability of patients affected by the pathology being studied.
ensure that the Investigator and staff have adequate training on study protocol and all related procedures, including the Investigational Medicinal Product/Investigational Product/Medical Device and the ICH-GCP, ISO1455 and any other applicable standards.
Interact with the Regulatory and submission team and support in collecting the documents or information necessary for the ethical and administrative submission.
Check that the enrolment schedule is in line with the study plan/projections and motivate
Investigators to achieve the planned recruitment targets.
Ensure delivery of study materials and products are available prior to study initiation.
Ongoing management of study materials, including study product(s), as foreseen for the specific study and as applicable (product supply and return, CRFs, laboratory material and samples, study documents, etc.).
Conduct regular on site and remote monitoring visits in accordance with the Monitoring Plan, the contract, OPIS/Sponsor SOPs/WIs as appropriate.
Ensure accuracy and completeness of data entered into OPIS/Sponsor systems and ensure that
Perform source data verification according to the Monitoring Plan or other similar documents.
Verify that Adverse Events and Serious Adverse Events have been reported according to OPIS and/or Sponsor procedures and in adherence to regulatory requirements.
0-12 Months of experience as CRA
~ Knowledge of ICH-GCP and ISO14155 and techniques for the monitoring of clinical studies and clinical investigations.
~ for CRA working in Italy, of Ministerial Decree in order to conduct interventional clinical trials)
~ Able to carry out all the activities related to the monitoring of clinical trials/clinical investigations, guaranteeing the security of information
~ Good knowledge of English language
~ Able to work independently under the supervision of the Project Managers and Clinical Operations Managers
~ Able to interact with the personnel of clinical studies and clinical investigations
Founded in 1998 in Italy and now operating at an international level, OPIS is a full-service science driven biotech focused CRO providing premium trial management for multi-country clinical trials, including state-of-the-art information technology solutions and innovative approaches to the increasing complexity and variety of current projects.
OPIS added value lies in its highly specialized professionals who can assist their clients using their deep know-how and experience to guarantee a top-quality level of Clinical Trial Management and ability to operate in a wide range of fields (medical writing, scientific and statistical consultancy for trial design, regulatory activities, pharmacovigilance, etc.) Please read the information notice on the processing of personal data in the candidates information section of our company website.
