Indero

Clinical Trial Manager II / Gestionnaire d’essais cliniques II, Canada, remote

Indero · Full Time · 2 days ago

Indero

🌎 Canada ⭐ 10+ yrs exp 💼 Healthcare

Responsible for the operational management and oversight of clinical investigative sites and monitoring deliverables for clinical trials. This includes training CRAs, identifying quality issues, and ensuring timelines and regulatory requirements are met.

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Strategist, Patient Recruitment & Site engagement (Romania)

Indero · Full Time · 3 days ago

Indero

🌎 Oman, Romania ⭐ 2-5 yrs exp 💼 Recruitment

Develop and implement project-level patient recruitment and site engagement strategies in collaboration with project teams. Monitor enrollment progress, create recruitment models, and design advertisement scripts and images following ethics guidelines.

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Strategist, Patient Recruitment & Site engagement (Argentina)

Indero · Full Time · 3 days ago

Indero

🌎 Argentina ⭐ 2-5 yrs exp 💼 Recruitment

Develop and implement project-level patient recruitment strategies and site engagement plans in collaboration with project teams. Monitor subject enrollment progress and create recruitment models and trackers to ensure study targets are achieved.

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Strategist, Patient Recruitment & Site engagement (Poland)

Indero · Full Time · 3 days ago

Indero

🌎 Poland ⭐ 2-5 yrs exp 💼 Recruitment

Develop and implement project-level patient recruitment and site engagement strategies in collaboration with project teams. Monitor enrollment progress, create recruitment models, and design advertisement materials while ensuring compliance with ethics committee guidelines.

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Strategist, Patient Recruitment & Site engagement (Germany)

Indero · Full Time · 3 days ago

Indero

🌎 Germany ⭐ 2-5 yrs exp 💼 Recruitment

Develop and implement project-level patient recruitment and site engagement strategies in collaboration with project teams. Monitor subject enrollment progress and create recruitment models and trackers to ensure study targets are achieved.

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Project Director, Dermatology & Rheumatology CRO, Poland

Indero · Full Time · 5 days ago

Indero

🌎 Spain ⭐ 10+ yrs exp 💼 Sales

Oversees a portfolio of clinical studies in dermatology and rheumatology, managing Project Managers and ensuring adherence to quality standards and regulatory requirements. Leads operational contributions to business development, proposal pricing, and client relationship management.

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Project Director, Dermatology & Rheumatology CRO, EU, Spain

Indero · Full Time · 5 days ago

Indero

🌎 Spain ⭐ 10+ yrs exp 💼 Sales

Oversees a portfolio of clinical studies in dermatology and rheumatology, managing Project Managers and ensuring adherence to quality standards and regulatory requirements. Leads operational contributions to business development, proposal pricing, and client relationship management.

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Project Director, Dermatology & Rheumatology CRO, Germany

Indero · Full Time · 5 days ago

Indero

🌎 Spain ⭐ 10+ yrs exp 💼 Sales

Oversees a portfolio of clinical studies in dermatology and rheumatology, managing Project Managers and ensuring adherence to quality standards and regulatory requirements. Leads operational contributions to business development, proposal pricing, and client relationship management.

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Project Director, Dermatology & Rheumatology CRO, EU

Indero · Full Time · 5 days ago

Indero

🌎 Germany ⭐ 10+ yrs exp 💼 Sales

Oversees a portfolio of clinical studies in dermatology and rheumatology, managing Project Managers and ensuring adherence to quality standards and regulatory requirements. Leads operational contributions to business development, proposal pricing, and client relationship management.

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Project Director, Dermatology & Rheumatology CRO, Argentina

Indero · Full Time · 5 days ago

Indero

🌎 Argentina ⭐ 10+ yrs exp 💼 Sales

Oversees a portfolio of clinical studies in dermatology and rheumatology, managing Project Managers and ensuring adherence to quality standards and regulatory requirements. Leads operational contributions to business development, proposal pricing, and client relationship management.

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Spécialiste, rédaction de propositions/Proposal Writer Specialist

Indero · Full Time · 21 days ago

Indero

🌎 Canada ⭐ 2-5 yrs exp 💼 Writing

Responsible for developing and writing scientific and technical content for study proposals and responding to RFIs. Coordinates with internal subject matter experts and external KOLs to ensure accurate, compelling, and compliant proposal documents.

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Clinical Trial Manager II, US, remote

Indero · Full Time · a month ago

Indero

🌎 United States ⭐ 10+ yrs exp 💼 Healthcare

The Clinical Trial Manager II oversees clinical investigative sites and manages clinical monitoring deliverables to ensure quality and timeline compliance. This includes mentoring CRAs, reviewing site visit reports, and developing clinical monitoring plans.

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Line Manager, Regulatory Affairs, Canada, remote

Indero · Full Time · a month ago

Indero

🌎 Canada ⭐ 2-5 yrs exp 💼 Legal

This role combines people leadership with operational delivery, overseeing regulatory submissions to Ethics Committees and Regulatory Authorities for clinical trials. The manager is responsible for resource management, team development, and ensuring compliance with regional regulatory guidelines.

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Medical Monitor Associate, Dermatology & Rheumatology, Argentina

Indero · Full Time · 2 months ago

Indero

🌎 Argentina ⭐ 2-5 yrs exp 💼 Healthcare

Provide medical, scientific, and administrative support to the medical monitoring team for clinical trials in dermatology and rheumatology. Responsibilities include reviewing safety data, coding adverse events, and supporting protocol development and business development activities.

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Senior Clinical Trial Manager, Canada or US, remote

Indero · Full Time · 2 months ago

Indero

🌎 Italy ⭐ 10+ yrs exp 💼 Healthcare

The Senior Clinical Trial Manager oversees clinical investigative sites and manages clinical monitoring deliverables to ensure quality and regulatory compliance. This includes mentoring CRAs, developing monitoring plans, and establishing corrective action plans for site performance issues.

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Business Applications Analyst, Argentina, remote,

Indero · Full Time · 2 months ago

Indero

🌎 Argentina ⭐ 2-5 yrs exp 💼 Others

Acts as the functional bridge between business users and enterprise systems by gathering requirements and configuring applications. Collaborates with development teams to implement scalable system enhancements and provides ongoing support and documentation.

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Statistical Programmer-Argentina

Indero · Full Time · 2 months ago

Indero

🌎 Argentina ⭐ 0-2 yrs exp 💼 Software Development

Responsible for developing and validating SDTM and ADaM datasets, as well as Tables, Listings, and Figures (TLFs) for clinical study reports. Collaborates with biostatistical teams to ensure deliverables meet ICH guidelines and regulatory requirements.

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Statistical Programmer-Romania

Indero · Full Time · 2 months ago

Indero

🌎 Oman, Romania ⭐ 0-2 yrs exp 💼 Software Development

Responsible for developing and validating SDTM and ADaM datasets, as well as producing Tables, Listings, and Figures (TLFs) for clinical study reports. The role involves collaborating with biostatistical teams to ensure deliverables meet ICH guidelines and regulatory requirements.

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Senior Statistical Programmer-Romania

Indero · Full Time · 2 months ago

Indero

🌎 Oman, Romania ⭐ 5-10 yrs exp 💼 Software Development

Lead the development, maintenance, and validation of SDTM and ADaM datasets, as well as Tables, Listings, and Figures (TLFs) for clinical trials. Collaborate with biostatistical teams to ensure deliverables meet ICH guidelines and regulatory requirements for submission packages.

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Statistical Programmer-Canada

Indero · Full Time · 2 months ago

Indero

🌎 Canada ⭐ 0-2 yrs exp 💼 Software Development

Responsible for developing and validating SDTM and ADaM datasets, as well as Tables, Listings, and Figures (TLFs) for clinical study reports. Collaborates with biostatistical teams to ensure deliverables meet ICH guidelines and regulatory requirements.

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Senior Statistical Programmer-Argentina

Indero · Full Time · 2 months ago

Indero

🌎 Argentina ⭐ 5-10 yrs exp 💼 Software Development

Lead the development, maintenance, and validation of SDTM and ADaM datasets, as well as Tables, Listings, and Figures for clinical trials. Collaborate with biostatistical teams to ensure deliverables meet ICH guidelines and regulatory requirements while mentoring junior programmers.

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Senior Statistical Programmer

Indero · Full Time · 2 months ago

Indero

🌎 Argentina ⭐ 5-10 yrs exp 💼 Software Development

Lead the development, maintenance, and validation of SDTM and ADaM datasets, as well as Tables, Listings, and Figures for clinical trials. Collaborate with biostatistical teams to ensure deliverables meet ICH guidelines and regulatory requirements for submission packages.

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Statistical Programmer

Indero · Full Time · 2 months ago

Indero

🌎 Argentina ⭐ 0-2 yrs exp 💼 Software Development

Develop, maintain, and validate SDTM and ADaM datasets, as well as Tables, Listings, and Figures (TLFs) for clinical study reports. Collaborate with biostatistical teams to ensure deliverables meet ICH guidelines and regulatory requirements.

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Statistical Programmer

Indero · Full Time · 2 months ago

Indero

🌎 Canada ⭐ 0-2 yrs exp 💼 Software Development

Responsible for developing and validating SDTM and ADaM datasets, as well as Tables, Listings, and Figures (TLFs) for clinical study reports. The role involves collaborating with biostatistical teams to ensure deliverables meet regulatory requirements and company SOPs.

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Statistical Programmer

Indero · Full Time · 2 months ago

Indero

🌎 Oman, Romania ⭐ 0-2 yrs exp 💼 Software Development

Responsible for developing and validating SDTM and ADaM datasets, as well as Tables, Listings, and Figures (TLFs) for clinical study reports. The role involves collaborating with biostatistical teams to ensure deliverables meet ICH guidelines and regulatory requirements.

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Senior Statistical Programmer

Indero · Full Time · 2 months ago

Indero

🌎 Oman, Romania ⭐ 5-10 yrs exp 💼 Software Development

Lead the development, maintenance, and validation of SDTM and ADaM datasets, as well as Tables, Listings, and Figures (TLFs) for clinical trials. Collaborate with biostatistical teams to ensure deliverables meet ICH guidelines and regulatory requirements for submission packages.

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Project Manager (Romania)

Indero · Full Time · 2 months ago

Indero

🌎 Oman, Romania ⭐ 2-5 yrs exp 💼 Product

The Project Manager oversees the initiation, planning, and execution of clinical research projects while ensuring compliance with budgets, timelines, and regulatory requirements. They coordinate between sponsors, vendors, and internal teams to manage site activation and project deliverables.

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Project Manager (Germany)

Indero · Full Time · 2 months ago

Indero

🌎 Germany ⭐ 2-5 yrs exp 💼 Product

The Project Manager oversees the initiation, planning, and execution of clinical research projects while ensuring compliance with budgets, timelines, and regulatory requirements. They serve as a primary contact for sponsors and vendors while coordinating site activation and monitoring activities.

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Project Manager (Poland)

Indero · Full Time · 2 months ago

Indero

🌎 Poland ⭐ 2-5 yrs exp 💼 Product

The Project Manager oversees the initiation, planning, and execution of clinical research projects while ensuring compliance with budgets, timelines, and regulatory requirements. Key duties include coordinating between departments, managing sponsor expectations, and overseeing site activation and patient recruitment activities.

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Administrative Assistant / Assistant(e) administrative

Indero · Full Time · 2 months ago

Indero

🌎 Canada ⭐ 0-2 yrs exp 💼 Data Entry

Provide comprehensive administrative support to the clinical research unit, including managing office supplies, archiving, and coordinating meetings. The role also involves reception duties such as welcoming patients, managing appointments, and supporting medical secretaries.

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Senior Regulatory Affairs Specialist-Germany

Indero · Full Time · 2 months ago

Indero

🌎 Germany ⭐ 2-5 yrs exp 💼 Legal

Lead global and multinational regulatory submissions for complex large clinical trials and manage sponsor-facing regulatory deliverables. Provide leadership on project timelines, regulatory strategy, and mentor junior colleagues within the regulatory team.

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Project Manager II (Poland)

Indero · Full Time · 2 months ago

Indero

🌎 Poland ⭐ 5-10 yrs exp 💼 Product

The Project Manager II is responsible for the end-to-end management of clinical trials, ensuring compliance with budgets, timelines, and regulatory standards. They act as the primary point of contact for sponsors and lead cross-functional teams to deliver high-quality study outcomes.

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Project Manager II (Germany)

Indero · Full Time · 2 months ago

Indero

🌎 Germany ⭐ 5-10 yrs exp 💼 Product

The Project Manager II is responsible for the initiation, planning, execution, and closure of clinical trials while ensuring compliance with budgets, timelines, and regulatory standards. They act as the primary contact for sponsors and lead cross-functional teams to ensure study deliverables are met.

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Project Manager II (Romania)

Indero · Full Time · 2 months ago

Indero

🌎 Oman, Romania ⭐ 5-10 yrs exp 💼 Product

The Project Manager II is responsible for the end-to-end management of clinical trials, ensuring compliance with budgets, timelines, and regulatory standards. They act as the primary point of contact for sponsors and lead cross-functional teams to deliver high-quality study outcomes.

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Future opportunities/Opportunités de carrière

Indero · Full Time · 3 months ago

Indero

🌎 Canada ⭐ 0-2 yrs exp 💼 Others

This is a general talent pool posting for future career opportunities at Indero. Candidates are invited to express their interest in joining the team for potential upcoming roles.

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Project Manager (Argentina)

Indero · Full Time · 3 months ago

Indero

🌎 Argentina ⭐ 2-5 yrs exp 💼 Product

The Project Manager oversees the initiation, planning, execution, and closure of clinical research projects while ensuring compliance with budgets, timelines, and regulatory standards. They serve as the primary contact for stakeholders and coordinate tasks across various departments to ensure successful site activation and study delivery.

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Project Manager I (Argentina)

Indero · Full Time · 3 months ago

Indero

🌎 Argentina ⭐ 2-5 yrs exp 💼 Product

The Project Manager I is responsible for tracking study budgets, project scope, and timelines while ensuring compliance with SOPs and regulatory requirements. They also communicate project information to stakeholders, coordinate tasks across departments, and assist in managing project resources and deliverables.

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Regulatory Affairs Associate-Romania

Indero · Full Time · 4 months ago

Indero

🌎 Oman, Romania ⭐ 0-2 yrs exp 💼 Legal

The Associate will support the preparation, tracking, and coordination of Ethics Committee (EC) and Regulatory Authority (RA) submissions, ensuring clinical trial documentation complies with regulations. Key tasks include assisting with documentation compilation, tracking timelines, coordinating with IRBs/IECs, and managing document formatting and submission processes.

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Regulatory Affairs Associate-Poland

Indero · Full Time · 4 months ago

Indero

🌎 Poland ⭐ 0-2 yrs exp 💼 Legal

The Regulatory Affairs Associate will support the preparation, tracking, and coordination of Ethics Committee (EC) and Regulatory Authority (RA) submissions, ensuring clinical trial documentation complies with regulations and internal timelines. Key duties include assisting in document compilation, maintaining regulatory trackers, coordinating with internal teams, and managing country-specific informed consent forms.

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Regulatory Affairs Specialist-Poland

Indero · Full Time · 4 months ago

Indero

🌎 Poland ⭐ 2-5 yrs exp 💼 Legal

The specialist will prepare and submit regulatory documentation, including Part I and/or Part II following EU CTR, ensuring compliance with regulations and meeting contractual timelines for clinical trial startup. Key duties involve coordinating regulatory timelines for CTIS submissions across EU, APAC, and North America, and reviewing external submissions for quality assurance.

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Regulatory Affairs Specialist-Romania

Indero · Full Time · 4 months ago

Indero

🌎 Oman, Romania ⭐ 2-5 yrs exp 💼 Legal

The specialist will prepare and submit regulatory documents, including Part I and/or Part II following EU CTR, ensuring compliance with regulations and meeting contractual timelines for clinical trial startup. This involves coordinating regulatory timelines across EU, APAC, and North America submissions and reviewing external documentation for quality.

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Strategist, Operational Strategy / Stratège de la stratégie opérationnelle (Canada)

Indero · Full Time · 4 months ago

Indero

🌎 Canada ⭐ 5-10 yrs exp 💼 Others

The Strategist is responsible for defining the operational strategy for new studies, including country selection, timelines, risk mitigation, and vendor needs, while preparing and reviewing commercial proposals for prospective clients. This role involves extensive interaction with internal and external stakeholders to gather requirements and ensure the strategy aligns with project goals and scope.

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Strategist, Operational Strategy (Poland)

Indero · Full Time · 4 months ago

Indero

🌎 Poland ⭐ 5-10 yrs exp 💼 Others

The Strategist is responsible for defining the operational strategy for new studies, including timelines, site needs, and risk mitigation, and preparing content for commercial proposals and bid defense meetings. This involves extensive interaction with internal and external stakeholders to gather requirements and demonstrate industry knowledge.

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Project Manager II / Gestionnaire de projet II (Canada)

Indero · Full Time · 4 months ago

Indero

🌎 Canada ⭐ 5-10 yrs exp 💼 Product

The Project Manager II is responsible for the successful initiation, planning, execution, monitoring, controlling, and closure of assigned clinical trials, ensuring compliance with budget, scope, timelines, SOPs, and regulatory requirements. This role involves serving as the main line of communication to stakeholders, providing input on feasibility and study design, and ensuring progress reporting on resources, budget, and timelines.

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Project Manager II (Argentina)

Indero · Full Time · 4 months ago

Indero

🌎 Argentina ⭐ 5-10 yrs exp 💼 Product

The Project Manager II holds overall responsibility for the successful initiation, planning, execution, monitoring, controlling, and closure of assigned clinical trials, ensuring compliance with budget, scope, timelines, and regulatory requirements. This role involves serving as the primary contact for the Sponsor, leading project deliverables preparation, managing study start-up activities, and overseeing quality and risk management.

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