Career Opportunities: Clinical Research Officer (68237)
JobLeads GmbH
España
hace 3 días

For more than 75 years, Grifols has worked to improve the health and well-being of people around the world. We are a global healthcare company that produces essential plasma-

derived medicines for patients and provides hospitals and healthcare professionals with the tools, information and services they need to deliver expert medical care.

Headquartered in Barcelona, Spain, Grifols has nearly 18,500 employees in 30 countries. Grifols' three main divisions - Bioscience, Diagnostic and Hospital -

develop, manufacture and market innovative products and services available in more than 100 countries. A leader in transfusion medicine, the Diagnostic Division is a global business focused on providing innovative solutions to help ensure the safety of the blood and plasma supply, detect human diseases and monitor therapies.

The division advances patient care with diagnostic solutions to improve disease detection and management, and simplify laboratory operations.

Grifols is a global healthcare company with more than 75 years of history improving the health and well-being of people around the world.

We produce essential plasma medicines for patients and provide hospitals, pharmacies, and healthcare professionals with tools, information, and services they need to efficiently deliver expert medical care.

We are present in more than 100 countries, with global headquarters in Barcelona, Spain, where the company was founded. As a company committed to serving people, we seek to hire and retain the very best employees.

Our day-today corporate culture reflects the Grifols Spirit, which is defined by our Values. Career Opportunities : Clinical Research Officer (68237) Req Id 68237 -

Posted 11 / 06 / 2018 - Region (1) - Country (1) - Location (1) - Temporary Full-Time - Clinical Trials Job Description Print Preview Apply Apply Using LinkedIn For more than 75 years, Grifols has worked to improve the health and well-

being of people around the world. We are a global healthcare company that produces essential plasma-derived medicines for patients and provides hospitals and healthcare professionals with the tools, information and services they need to deliver expert medical care.

Headquartered in Barcelona, Spain, Grifols has nearly 18,500 employees in 30 countries. Grifols' three main divisions - Bioscience, Diagnostic and Hospital -

develop, manufacture and market innovative products and services available in more than 100 countries. A leader in transfusion medicine, the Diagnostic Division is a global business focused on providing innovative solutions to help ensure the safety of the blood and plasma supply, detect human diseases and monitor therapies.

The division advances patient care with diagnostic solutions to improve disease detection and management, and simplify laboratory operations.

WHO WE ARE Grifols is a global healthcare company with more than 75 years of history improving the health and well-being of people around the world.

We produce essential plasma medicines for patients and provide hospitals, pharmacies, and healthcare professionals with tools, information, and services they need to efficiently deliver expert medical care.

We are present in more than 100 countries, with global headquarters in Barcelona, Spain, where the company was founded. As a company committed to serving people, we seek to hire and retain the very best employees.

Our day-today corporate culture reflects the Grifols Spirit, which is defined by our Values. From the Clinical Development department we are looking for a Clinical Research Officer.

YOUR TASK AND RESPONSABILITIES Executes studies in one or more assigned therapeutic area(s) from early phase and up to the market authorization.

Manages timelines and quality of deliverables for assigned study(ies). Primary Responsibilities for role :

  • Executes studies in one or more assigned therapeutic area(s) from start formal development and up to the market authorization.
  • Manages timelines and quality of deliverables for assigned study(ies).

  • Participates in clinical trial design.
  • Orchestrates relationships with external vendors (e.g., CROs) providing clinical input / review to clinical documents and ensures the integrity of clinical data (e.
  • g., protocols, investigator brochures, clinical study reports).

  • Drafts or provides review / input for publications from clinical study managing clinical timelines and external resources against the approved CDP in collaboration with his / her line manager.
  • Maintains good knowledge of the literature for the indication being studied and reviews and summarizes relevant literature for the therapeutic area of interest, as necessary.
  • Provides review / input of clinical study reports from clinical studies and interprets the data from tables, listings and figures to incorporate into written and diagrammatic format to support the key medical / scientific messaging for external reviewers.
  • Oversees third party vendors (e.g., CROs, central labs and trains them on SOPs, as necessary.
  • Manages the vendor's performance, including on time study completion, Budget adherence, and quality deliverables along with the senior management participating in development of vendor specifications to ensure accurate interpretation of the protocol requirements (e.
  • g. processes and data collection).

  • Attends across functional Project team meetings like collaborate with Biometry to ensure timely data transfers for data cleaning, review and analysis and with the Manager, Clinical Supplies to ensure timely manufacturing, packaging, labeling, shipping of clinical trial supplies for which the incumbent is responsible.
  • Offers guidance to resolve escalated study conduct issues and provides clinical responses to questions from study center personnel, regulatory authorities and institutional review boards / ethics committees maintains awareness of SAEs that are reported.
  • Presents clinical data, and ensures accuracy of data presented verbally or in written documentation.
  • Supports the development of study status presentation materials during internal management and advisory meetings.
  • Identifies risks, mitigations, opportunities and contingency plans for assigned study (ies).
  • Participates and contributes to internal and external training for clinical trials (e.g. kick-off meeting, Investigator meeting). WHO YOU ARE
  • Life Sciences Degree. Master Degree in Clinical Development would be a plus
  • A minimum of 2 years in a similar role in international CRO or pharmaceutical company overseeing / managing international studies
  • Native level of Spanish and Advanced in English
  • Ability and willingness to travel internationally, up to 25% of the time
  • Good knowledge of Microsoft Office, eTMF, and EDC platforms. WHAT WE OFFER It is a brilliant opportunity for you, Grifols is fully aware that its employees are one of its major assets.
  • We are committed to maintaining an atmosphere that encourages all our employees to develop their professional careers in an excellent working environment.

    Information about Grifols is available at www.grifols.com. If you are interested in joining our company and you have what it takes for such an exciting position, then don't hesitate to apply! We look forward to receiving your application! Grifols is an equal opportunity employer.

    Contract of Employment : Temporary position Location : Sant Cugat del Vallès Learn more about Grifols Apply Apply Using LinkedIn Email this job to a friend The job has been sent to Please provide the information below Job title : *Your email address : *Your friend's email address : Message : Maximum character limit : 1000 *Confirm you are not a robot : * Life Sciences Degree.

    Master Degree in Clinical Development would be a plus

  • A minimum of 2 years in a similar role in international CRO or pharmaceutical company overseeing / managing international studies
  • Native level of Spanish and Advanced in English
  • Ability and willingness to travel internationally, up to 25% of the time
  • Good knowledge of Microsoft Office, eTMF, and EDC platforms.It is a brilliant opportunity for you, Grifols is fully aware that its employees are one of its major assets.
  • We are committed to maintaining an atmosphere that encourages all our employees to develop their professional careers in an excellent working environment.

    Information about Grifols is available at www.grifols.com. If you are interested in joining our company and you have what it takes for such an exciting position, then don't hesitate to apply!

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