Indero
This role is a key partner in designing, administering, and continuously improving compensation programs aligned with organizational objectives. You will lead compensation analysis, market benchmarking, salary structure governance, annual compensation cycles, and pay equity activities, while providing expert guidance to…
The Statistical Programmer will be responsible for the development, maintenance, and validation of aCRFs, as well as of specifications and statistical programming of SDTMs, ADaMs (or derived datasets, as applicable), Tables, Listings, and Figures (TLFs), and submission packages required for…
This role is a key partner in designing, administering, and continuously improving compensation programs aligned with organizational objectives. You will lead compensation analysis, market benchmarking, salary structure governance, annual compensation cycles, and pay equity activities, while providing expert guidance to…
The Clinical Scientist is responsible for medical writing activities at Innovaderm. The individual will author or contribute to development of clinical and regulatory documents (synopsis, study protocols, statistical analysis plans, clinical study reports), as well as scientific publications. This role…
The Clinical Data Coordinator will participate in various clinical data management activities required to ensure that data captured in clinical trials undertaken, or managed by Indero, are collected, managed and reported clearly, accurately and securely. In addition, this position is…
The Clinical Scientist is responsible for medical writing activities at Innovaderm. The individual will author or contribute to development of clinical and regulatory documents (synopsis, study protocols, statistical analysis plans, clinical study reports), as well as scientific publications. This role…
The Project Director is responsible for oversight of the conduct of a program or portfolio of clinical studies or large global multicentered trials with large study budgets. The portfolio may comprise studies for specific customers, and/or a group of studies…
*** Please note that this is an 18 month contract *** Reporting to AP/AR Manager, the Team Lead, Project Account Payable is responsible for helping and supporting the Site payment team on their day to day activities, reconciling general ledger…
Please note that this is an 18 month contract Reporting to AP/AR Manager, the Team Lead, Project Account Payable is responsible for helping and supporting the Site payment team on their day to day activities, reconciling general ledger and projects…
The Project Director is responsible for oversight of the conduct of a program or portfolio of clinical studies or large global multicentered trials with large study budgets. The portfolio may comprise studies for specific customers, and/or a group of studies…
The Principal Biostatistician will act as Lead Biostatistician on multiple phase 1 to 4 clinical trials and/or Biostatistical Oversight for programs of phase 1 to 4 clinical trials, providing input into the statistical sections of protocols (incl. sample size calculation/…
The Associate Project Manager is involved in all phases of clinical trial project management. This person works closely with the Project Manager and functional team members. The Associate Project Manager is responsible for tracking the study budget, project scope and…
The Project Coordinator works with Project Managers, Clinical Trial Managers, Site Selection Team and Clinical Research Associates (CRA) to provide administrative and coordinating support for site activation activities and other site level deliverables through all phases of the clinical trial…
The role of the Sr. Auditor, Clinical Quality and Compliance is to act as lead person in the establishing audit plans, assessing/securing compliance in study conduct and to provide strong support to operations via GxP consultation. This role will be…
The eCOA and RTSM Application Specialist is responsible for supporting the design, deployment, configuration, and oversight of electronic Clinical Outcome Assessment (eCOA) solutions—including ePRO, eConsent, and other patient centric electronic data capture tools— and of Randomization and Trial Supply Management…
The Research Practical Nurse provides assistance to clinical research coordinators during visits to research subjects. This role will be perfect for you if: You have a Licensed Practical Nurses degree; You have an interest for the clinical research; RESPONSABILITIES More…
THIS IS A TEMPORARY POSITION FOR ONE YEAR MATERNITY LEAVE The Human Resources Specialist provides comprehensive support to the Human Resources team in executing key HR processes and initiatives throughout the employee lifecycle. Acting as a central point of coordination,…
As the Office Coordinator, you will be the administrative backbone of our organization. You will play a key role in supervising support activities while collaborating with different departments to optimize processes and assist management in achieving strategic objectives. This position…
Please note that this is a temporary contract until end of February The Patient Recruitment Assistant is responsible for providing patients with information on clinical research studies and verifying their eligibility for various research project. More specifically, the Patient Recruitment…
Projects Managers are crucial to the success of Clinical Trials managed by Indero. They are the main point of contact internally as well as externally, ensuring all activities and deliverables are completed on time, on budget, and as expected. Great…
THIS IS A TEMPORARY POSITION FOR ONE YEAR MATERNITY LEAVE The Human Resources Specialist provides comprehensive support to the Human Resources team in executing key HR processes and initiatives throughout the employee lifecycle. Acting as a central point of coordination,…
THIS IS A TEMPORARY POSITION FOR ONE YEAR MATERNITY LEAVE The Human Resources Specialist provides comprehensive support to the Human Resources team in executing key HR processes and initiatives throughout the employee lifecycle. Acting as a central point of coordination,…
Clinical Trial Manager II (CTM II), Dermatology & Rheumatology, Canada The Clinical Trial Manager II (CTM II), Dermatology & Rheumatology is responsible for the operational management and oversight of the clinical investigative sites as well as the clinical monitoring deliverables…
As a Senior Clinical Data Manager, you will ensure that data captured in multiple clinical trials undertaken or managed by Indero is collected, managed, and reported clearly, accurately and securely. This role will be perfect for you if: You want…
The Regulatory Documents Assistant will establish and maintain the Sponsor electronic or paper Trial Master File (TMF) throughout the life of the trial and will perform record review of essential documents for accuracy and quality according to ICH GCP. The…
As a Senior Clinical Data Manager, you will ensure that data captured in multiple clinical trials undertaken or managed by Indero is collected, managed, and reported clearly, accurately and securely. This role will be perfect for you if: You want…
As a Senior Clinical Data Manager, you will ensure that data captured in multiple clinical trials undertaken or managed by Indero is collected, managed, and reported clearly, accurately and securely. This role will be perfect for you if: You want…
As the Office Coordinator, you will be the administrative backbone of our organization. You will play a key role in supervising support activities while collaborating with different departments to optimize processes and assist management in achieving strategic objectives. This position…
Clinical Trial Manager II (CTM II), Dermatology & Rheumatology, Canada The Clinical Trial Manager II (CTM II), Dermatology & Rheumatology is responsible for the operational management and oversight of the clinical investigative sites as well as the clinical monitoring deliverables…
The Associate Project Manager, Early Phase and Translational Research (APM, EPTR) ensures the successful initiation, planning, execution, monitoring, controlling and closure of assigned Early Phase clinical research projects. In addition, the APM, EPTR is responsible for the operational management and…
The Senior Project Manager, Early Phase and Translational Research (Sr. PM, EPTR) oversees and manages domestic, regional and/or international projects. The senior project manager is responsible for developing and managing project teams, communications, risk, scope, schedule, cost, quality, and stakeholders,…
The Senior Project Coordinator works with Project Managers, Clinical Trial Managers, Site Selection Team and Clinical Research Associates (CRA) to provide administrative and coordinating support for site activation activities and other site level deliverables through all phases of the clinical…
Reporting to the Sr. Director, Operational Strategy, the Strategist, Operational Strategy is responsible, in concert with the assigned Project Director, for defining the operational strategy (countries/sites/timelines/key project success factors, outsourcing vendor needs, risk identification, and mitigation strategies, etc.), preparation and…
The Office Administrator supervises the administrative activities from different departments. He is also responsible for providing administrative support to the management of the clinical research unit. ?RESPONSIBILITIES More specifically, the Team leader, Administration must: Supervise the Administrative Assistants team; and…
The Medical Monitor Dermatology provides medical and scientific support to clinical research programs. The Medical Monitor will perform thorough data review to ensure data integrity and subject safety oversight, and will communicate with sites, investigators, and internal project team members…
Projects Managers with experience in Rheumatology are crucial to the success of Clinical Trials managed by Innovaderm. They are the main point of contact internally as well as externally, ensuring all activities and deliverables are completed on time, on budget,…