6 publicaciones de empleo destacadas de clinical scientist, clinical science, cronos en buenos aires, b (¡Están contratando!)

Site Activation Manager
IQVIA —Buenos Aires, Buenos Aires
- Tiempo completo
Internal Account Director (Recruitment & Retention)
サイネオス・ヘルス —Buenos Aires, Buenos Aires
Associate Project Services Manager
IQVIA —Buenos Aires, Buenos Aires
- Tiempo completo
(Senior) Data Team Lead
IQVIA —Buenos Aires, Buenos Aires
- Tiempo completo
Site Contracts Specialist with clinical trials experience Home-Based in Argentina
サイネオス・ヘルス —Buenos Aires, Buenos Aires
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RAM Reporting Programmer II
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Site Activation Manager

IQVIA -
Buenos Aires, Buenos Aires

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Detalles del empleo

Tiempo completo

Descripción completa del empleo

Buenos Aires, Argentina | Full time | Home-based | R1546189

Job Overview
Direct and manage the execution of the strategic, operational and financial delivery of required Site Activation activities, including but not limited to Site ID and Selection, Ethics and Regulatory processes and Site Contracting for assigned studies as determined by Company, scope of work and/or sponsor requirements.

Essential Functions

Provides strategic planning and project oversight accelerating Site Activation through best in class project management to ensure fast site activation for patient enrollment, responsibilities may include; Accountable for multiple regions.
Support and/or participate in pre-award/bid defense activities.
Oversee the execution of Start Up (including pre-award through Site Activation) and/or Lifecycle Maintenance for assigned projects in accordance with the agreed start up strategy, adhering to agreed project timelines and in compliance with regulatory requirements (International Conference on Harmonization (ICH)-Good Clinical Practice (GCP), protocol, customer requirements, and internal policies.
Study Delivery Scope minimum expectations: accountable for multiple regions or Global SAM project oversight responsibilities.
Develop, implement and maintain the Site Activation Management Plan according to the Scope of Work and Project Plan, within the agreed project strategy, resolving project related issues where required.
Collaborate with key stakeholders both internal and external, through effective communication and resolution management, including communication with regions and countries, to successfully deliver the agreed project scope in compliance with the Site Activation Management Plan.
Execute operational strategy/ expectations for maintenance of clinical study approvals, authorizations and review/ negotiation of contracts and essential documents.
Assess and review the regulatory landscape and contribute to the collection, interpretation, analysis and dissemination of accurate regulatory intelligence to support assigned studies and wider company, as required.
Determine regulatory strategy/expectations and parameters for submissions and all necessary authorizations. Identify regulatory complexity and challenges and offer creative and practical solutions to support the bid process and subsequent execution of the Site Activation Management Plan.
Provide ongoing updates and reporting to various levels of the organization, both study team and in some cases senior level colleagues.
Ensure accurate completion and maintenance of internal systems, databases, tracking tools, timelines and project plans with project specific information.
Create and/or review technical and administrative documentation to support business development and enable study initiation and maintenance, as required.
Adhere to quality standards, regulated and Company specific through the duration of the trial period.
Mentor and coach colleagues as required: mentor to Grade 140.
May take a lead role in developing long standing relationships with preferred IQVIA customers: Maintain and develop the customer relationship through study teamwork and support providing input to customer level processes and/or initiatives , attend Early Engagement Customer or Partnership Meetings if required.
Deliver presentations/training to clients, colleagues and professional bodies, as required.
Contribute to initiatives that affect positive change within the department and organization: support department and organizational initiatives.

Qualifications

Bachelor's Degree Life sciences or related field Req
At least 5 years with 2 years of lead experience in a scientific or clinical environment. Req
Demonstrable experience in an international role; or equivalent combination of education, training and experience. Req

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

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clinical scientist, clinical science, cronos empleos en buenos aires, b

Site Activation Manager

Internal Account Director (Recruitment & Retention)

Associate Project Services Manager

(Senior) Data Team Lead

Site Contracts Specialist with clinical trials experience Home-Based in Argentina

RAM Reporting Programmer II

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