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IQVIA
Sr. Site Activation Specialist, IQVIA BiotechIQVIA • Toronto, Ontario, Canada
Sr. Site Activation Specialist, IQVIA Biotech

Sr. Site Activation Specialist, IQVIA Biotech

IQVIA • Toronto, Ontario, Canada
12 days ago
Salary
CA$78,800.00 yearly
Job type
  • Full-time
  • Part-time
Job description

Job Overview
Perform tasks at a country level associated with Site Activation (SA) activities in accordance with applicable local and/or international regulations standard operating procedures (SOPs) project requirements and contractual/budgetary guidelines. May also include maintenance activitie. Developing professional individual contributor who works under moderate oversight and supervision. Responsible for making recommendations for enhancements in systems and processes to solve problems or improve effectiveness of job area. Problems faced are general and may require understanding of broader set of issues but are not complex.

Essential Functions
Under general supervision serve as Single Point of Contact (SPOC) in assigned studies for investigative sites Site Activation Manager (SAM) Project Management team and other departments as necessary. Ensure adherence to standard operating procedures (SOPs) Work Instructions (WIs) quality of designated deliverables and project timelines.
Perform feasibility site ID start up and site activation activities according to applicable regulations SOPs and work instructions. Distribute completed documents to sites and internal project team members.
Prepare site documents reviewing for completeness and accuracy.
Ensure accurate completion and maintenance of internal systems databases and tracking tools with project specific information.
Review and provide feedback to management on site performance metrics.
Review establish and agree on project planning and project timelines. Ensure monitoring measures are in place and implement contingency plan as needed.
Inform team members of completion of fesibility site ID regulatory and contractual documents for individual sites.
Review track and follow up the progress the approval and execution of documents questionnaires CDA/SIF regulatory ethics Informed Consent Form (ICF) and Investigator Pack (IP) release documents in line with project timelines.
Provide local expertise to SAMs and project team during initial and on-going project timeline planning.
Perform quality control of documents provided by sites.
May have direct contact with sponsors on specific initiatives.

Qualifications
Bachelors Degree Life science or related field Req And
Other 3 years clinical research or other relevant experience; or equivalent combination of education training and experience.
3 years clinical research experience including 1 year experience in a leadership capacity. Equivalent combination of education training and experience. Req

IQVIA est un fournisseur mondial de premier plan de services de recherche clinique dinformations commerciales et de renseignements sur les soins de santé pour les secteurs des sciences de la vie et de la santé. IQVIA se consacre à accélérer le développement et la commercialisation de traitements médicaux innovants pour aider à améliorer les résultats des patients et la santé de la population dans le monde entier. Pour en savoir plus visitez

IQVIA est fière dêtre un employeur souscrivant au principe de légalité daccès à lemploi. Tous les candidats qualifiés seront pris en considération pour un emploi sans égard à la race la couleur la religion le sexe lorientation sexuelle lidentité de genre lorigine nationale le handicap lâge létat matrimonial ou tout autre statut protégé par la loi applicable. Des mesures dadaptation pour les candidats handicapés sont disponibles sur demande dans tous les aspects du processus de recrutement. Si vous avez un handicap qui nécessite une mesure dadaptation nous vous encourageons à contacter notre équipe dacquisition de talents au afin quIQVIA puisse soutenir votre participation au processus de recrutement.

IQVIA sengage à faire preuve dintégrité dans son processus de recrutement et applique une politique de tolérance zéro en matière de fraude des candidats. Toutes les informations et toutes les qualifications soumises dans votre candidature doivent être véridiques et complètes. Toute fausse déclaration présentation trompeuse ou omission importante au cours du processus de recrutement entraînera la disqualification immédiate de votre candidature ou la cessation demploi si elle est découverte ultérieurement conformément aux lois applicables. Nous apprécions votre honnêteté et votre professionnalisme.

Veuillez noter quil est possible que nous utilisions lintelligence artificielle (IA) dans le traitement de votre candidature. Cependant nous utilisons lIA uniquement pour aider notre équipe de recrutement à sélectionner ou à évaluer les candidatures et non pas pour remplacer la prise des décisions par les membres de notre équipe.

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

IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race color religion sex sexual orientation gender identity national origin disability age marital status or any other status protected by applicable law. Accommodations for applicants with disabilities are available in all aspects of the recruitment process upon request. If you have a disability that requires an accommodation we encourage you to contact our Talent Acquisition Team at: so that IQVIA can support your participation in the recruitment process.

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.

Please note that we may use artificial intelligence (AI) in the processing of your application. However we only use AI to assist our recruitment team with the screening or assessment of candidacies and not as a substitute for human decision-making.

La fourchette salariale de base potentielle pour ce poste annualisée est de $78800.00 - $105000.00. Le salaire de base réel offert peut varier selon plusieurs facteurs notamment les qualifications liées à lemploi telles que les connaissances les compétences la formation et lexpérience; lemplacement; et/ou lhoraire (temps plein ou temps partiel). Selon le poste offert des régimes dincitation des primes et/ou dautres formes de rémunération peuvent être proposés en plus dune gamme davantages sociaux liés à la santé au bien-être et/ou dautres bénéfices.

The potential base pay range for this role when annualized is $78800.00 - $105000.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge skills education and experience; location; and/or schedule (full or part-time). Dependent on the position offered incentive plans bonuses and/or other forms of compensation may be offered in addition to a range of health and wellness and/or other benefits.

Required Experience:

Senior IC


Employment Type : Full-Time
Experience: years
Vacancy: 1
Monthly Salary Salary: 78800 - 105000
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Sr. Site Activation Specialist, IQVIA Biotech • Toronto, Ontario, Canada

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