IQVIA

Chercheur(se) clinicien(ne), Sciences cliniques, Cronos -- Clinical Scientist, Clinical Science, Cronos

IQVIA • $97K — $147K *
Mississauga, ON L4T 0A1In-Person
Healthcare
Less than 5 years of experience
2 months ago
Job Overview by Ladders

Qualifications

  • Master's degree in Psychology, Counseling, Psychiatric, Nursing or Social Work, or equivalent.
  • At least 3 years experience with psychiatric or neuropsychiatric populations.
  • Minimum 3 years experience administering psychiatric assessments and structured clinical interviews.
  • Preferred experience with central nervous system (CNS) trials.
  • Advanced proficiency in English.

Responsibilities

  • Attend sponsor meetings as required.
  • Conduct protocol reviews for clinical studies.
  • Develop training materials for raters according to assignment.
  • Perform quality control reviews of clinician's work on studies.
  • Provide feedback to clinical trial raters through calls and emails.
  • Review clinical trial site data and determine necessary interventions with Clinical Managers/Directors.
  • Support the development of standardized operational procedures and work instructions.

Benefits

  • Opportunity to work in a fast-paced, dynamic environment.
  • Collaboration with a highly skilled clinical science team.
  • Contribution to innovative global clinical trials.
  • Access to comprehensive training and professional development opportunities.
  • Engagement with a diverse range of stakeholders.
Full Job Description
Chercheur(se) clinicien(ne) - Sciences cliniques, Cronos

Rôles et responsabilités

L'équipe Sciences cliniques de Cronos assure la supervision et l'expertise scientifiques nécessaires pour garantir la qualité, la cohérence et la fiabilité des données d'évaluation des résultats dans les essais cliniques internationaux. L'équipe assure la formation et l'étalonnage des évaluateurs, examine les données d'évaluation, identifie et gère les risques liés aux mesures et collabore étroitement avec les équipes Opérations et Technologie des études afin de promouvoir une administration standardisée, la conformité réglementaire et des indicateurs de résultats de haute qualité dans toutes les études.

En tant que chercheur(se) clinicien(ne) au sein de l'équipe Sciences cliniques de Cronos, vos responsabilités seront les suivantes :
  • Assister aux réunions avec les promoteurs, au besoin.
  • Effectuer une revue des protocoles.
  • Contribuer au développement de la méthodologie de formation des évaluateurs.
  • Élaborer les supports de formation des évaluateurs, selon les directives.
  • Effectuer des contrôles de qualité du travail des cliniciens sur les études qui leur sont attribuées.
  • Fournir une rétroaction aux évaluateurs d'essais cliniques par téléphone et/ou par courriel.
  • Effectuer des analyses des données des centres d'essais cliniques et déterminer les interventions nécessaires, en consultation avec les gestionnaires/directeurs cliniques s'il y a lieu.
  • Contribuer à la création de diapositives illustrant les problèmes et tendances identifiés dans les données de l'étude.
  • Faire éventuellement office de principal(e) représentant(e) clinique pour les interactions avec les promoteurs.
  • Contribuer à l'élaboration de méthodologies d'intervention et du matériel de soutien.
  • Collaborer avec la direction clinique et le personnel, le cas échéant, en vue d'identifier, de suivre et de mettre à jour les livrables cliniques.
  • Communiquer directement avec les fournisseurs et clients externes, au besoin.
  • Contribuer éventuellement à l'élaboration de procédures opérationnelles normalisées et de directives de travail, selon les recommandations de la direction clinique.
  • Soutenir les activités cliniques, en assurant l'exécution et le suivi des activités liées au service ou au produit.
  • Communiquer efficacement les indicateurs du département clinique et des services/produits concernés à la direction clinique.
  • Exécuter les activités de préparation des données (nettoyage, transformation et validation) et réaliser les tâches d'analyse de données adaptées au niveau d'expérience.
  • Maîtriser l'utilisation de MS Office (Word, Excel, Outlook, PowerPoint) et de SharePoint dans l'exécution des tâches professionnelles.
  • Autres tâches attribuées.


À propos de vous

Les candidat(e)s souhaitant rejoindre l'équipe doivent respecter les critères suivants :

CONNAISSANCES, COMPÉTENCES ET APTITUDES REQUISES
  • Capacités avérées de résolution de problèmes.
  • Esprit d'initiative, excellentes aptitudes relationnelles et fort esprit d'équipe et capacité de travailler de manière autonome avec l'ensemble de nos collaborateurs.
  • Solides compétences informatiques, notamment dans l'utilisation des applications Microsoft Office.
  • Capacité à établir des relations d'affaires solides et à exercer une influence auprès des principales parties prenantes à tous les niveaux de l'entreprise.
  • Maîtrise de Microsoft Excel (niveau intermédiaire).
  • Capacité à assimiler rapidement différents types de renseignements provenant de sources variées pour une prise de décision efficace.
  • Excellentes compétences en communication écrite et orale, notamment une maîtrise de la rédaction technique et des règles grammaticales.
  • Excellente attention aux détails et grande précision.
  • Aptitude à communiquer avec assurance et à présenter efficacement des informations à l'équipe interne.
  • Capacité à travailler dans un environnement dynamique et aptitude avérée à gérer efficacement plusieurs tâches et projets.
  • Forte capacité d'initiative individuelle.
  • Solides compétences organisationnelles.
  • Engagement fort envers la qualité.
  • Capacité à établir et à entretenir des relations de travail efficaces avec les collègues, les gestionnaires et les clients.


FORMATION ET EXPÉRIENCE MINIMALES REQUISES
  • Détenir au minimum une maîtrise (MA/MS) en psychologie, counseling, psychiatrie, sciences infirmières ou travail social, ou l'équivalent.
  • Au moins 3 ans d'expérience auprès de populations psychiatriques (ex. : schizophrénie, trouble dépressif majeur) et/ou neuropsychiatriques (ex. : maladie d'Alzheimer).
  • Au moins 3 ans d'expérience dans l'administration d'évaluations psychiatriques, d'échelles d'évaluation et/ou d'entrevues cliniques structurées.
  • Une expérience préalable dans le cadre d'essais sur le système nerveux central (SNC) constitue un atout.
  • Maîtrise avancée de l'anglais.


Clinical Scientist - Clinical Science, Cronos

Role & Responsibilities

The Cronos Clinical Science team provides scientific oversight and expertise to ensure the quality, consistency, and reliability of clinical outcome assessment data in global clinical trials. The team supports rater training and calibration, reviews assessment data, identifies and addresses measurement risk, and partners closely with Study Operations and Technology to promote standardized administration, regulatory compliance, and high-quality endpoints across studies.

As a Clinical Scientist in the Cronos Clinical Science team, your responsibilities will include:
  • Attend sponsor meetings, as required.
  • Conduct protocol review.
  • Contribute to the development of rater training methodology.
  • Develop rater training materials, as assigned.
  • Conduct Quality Control reviews of clinician work on assigned studies.
  • Provide feedback to clinical trial raters via calls and/or emails.
  • Conduct reviews of clinical trial site data and make determinations regarding required interventions, in consultation with Clinical Managers/Directors as needed.
  • Assist with creation of slides indicating issues and trends identified in study data.
  • May serve as the primary clinical representative for sponsor interactions.
  • Assist with development of intervention methodologies and supporting materials.
  • Coordinate with Clinical Leadership and staff, as appropriate, to identify, track, and update clinical deliverables.
  • Communicate directly with external vendors/clients, as required.
  • May contribute to the development of Standard Operating Procedures and Work Instructions, under the guidance of Clinical Leadership.
  • Support Clinical activities, ensuring appropriate execution and tracking of activities related to the service/product.
  • Effectively communicate Clinical Department and assigned service/product metrics to Clinical Leadership.
  • Execute data preparation activities-including cleaning, transformation, and validation-and perform data analytics tasks appropriate to experience level.
  • Utilize MS Office (Word, Excel, Outlook, Powerpoint) and SharePoint proficiently in execution of job tasks.
  • Other duties as assigned.


About You

Candidates interested in joining the team should have:

REQUIRED KNOWLEDGE, SKILLS AND ABILITIES
  • Proven problem-solving skills.
  • A self-starting mind-set with excellent team-based interpersonal skills with the ability to work independently with the full spectrum of our people.
  • Strong computer skills, including Microsoft Office applications.
  • Ability to build strong business relationships and influence with key stakeholders at all levels within the business.
  • Proficiency in Microsoft Excel (intermediate).
  • Ability to rapidly assimilate multiple types of information from a variety of sources for effective decision making.
  • Excellent written and oral communication skills including grammatical/technical writing skills.
  • Excellent attention and accuracy with details.
  • Ability to confidently communicate with and effectively present information to internal team.
  • Must be able to work in a fast-paced environment with demonstrated ability to effectively manage multiple tasks and projects.
  • Strong individual initiative.
  • Strong organizing skills.
  • Strong commitment to quality.
  • Ability to establish and maintain effective working relationships with coworkers, managers and clients.


MINIMUM REQUIRED EDUCATION AND EXPERIENCE
  • Minimum of a Master's degree (MA/MS) in Psychology, Counseling, Psychiatric, Nursing or Social Work, or equivalent.
  • Minimum of 3 years of experience with psychiatric populations (e.g., schizophrenia, major depressive disorder) and/or neuropsychiatric populations (e.g., Alzheimer's Dementia).
  • Minimum of 3 years of experience administering psychiatric assessments, ratings scales and/or structured clinical interviews.
  • Previous experience working with central nervous system (CNS) trials preferred.
  • Advanced English proficiency.

About IQVIA

Innovex offers superior and creative advice to corporations. In addition, they raised venture capital for our own affiliate companies, in addition to having assisted clients in fund-raising efforts, new venture outreaches, and financing. Their engineers and technical staff offer varied backgrounds in manufacturing, high tech, product design, quality control, safety, biomechanics, and robotics.

IQVIA Careers

Join the vibrant team at IQVIA, a leading global provider of advanced analytics, technology solutions, and clinical research services to the healthcare industry. IQVIA is recognized for its commitment to innovation, leadership in healthcare, and a culture that celebrates diversity and inclusion.

Work You’ll Do

At IQVIA, we offer job opportunities that empower you to leverage your skills and drive healthcare forward. Become part of a team that thrives on innovation and the pursuit of operational excellence, helping to improve patient outcomes across the globe.

Transform Your Career

IQVIA is the place where you can transform the world of healthcare while advancing your career. With a variety of positions available, from research and development to business analytics, IQVIA is at the forefront of the industry. Our leadership is committed to fostering a culture of growth and professional development, making IQVIA a prime environment for both seasoned professionals and those seeking an internship to kickstart their career.

Innovative Work Environment

Join over 50,000 dedicated professionals in a dynamic environment where technology meets healthcare. At IQVIA, innovation isn’t just a buzzword; it's the backbone of how we solve complex challenges. With cutting-edge resources and a collaborative global team, your work at IQVIA directly contributes to advancements in life sciences.

Career Development and Benefits

IQVIA believes in nurturing its team members not just as employees but as individuals seeking to grow their careers. We support this with unmatched benefits, diversity training, and opportunities for leadership development. Our commitment to your career growth is matched by our dedication to providing a supportive and inclusive workplace.

Explore Job Opportunities

Whether you’re looking for a full-time position, part-time work, or a graduate internship, IQVIA offers a range of employment options to match your career ambitions. Our hiring process is designed to be transparent and engaging, helping you to understand where your skills can best be utilized within the company.

Networking and Professional Development

At IQVIA, networking and professional development are part of our DNA. Engage with industry leaders, participate in global conferences, and take advantage of our in-house training programs designed to enhance your skills and advance your career.

Stay Connected

Join Our Team Search open positions that match your skills and interests. We look for passionate, curious, creative, and solution-driven team players. Explore the diverse job opportunities at IQVIA and find where you can make an impact.

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Personalize your subscription to receive job alerts, latest news, and insider tips tailored to your preferences. Discover the exciting and rewarding career opportunities that await at IQVIA. Embark on a journey of growth, innovation, and leadership at IQVIA. Shape your future in an environment that values diversity and fosters professional development. Join IQVIA today and transform healthcare through the power of information and technology.
Learn more about IQVIA
Size
82,000 employees
Market Cap
$37.5 billion
Industry
Pharmaceuticals & Biotech
Net Income
$279 million
Founded
2016
5 Year Trend
+15.3%
Revenue
$11.3 billion
NASDAQ
IQV
* Ladders Estimates

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