Jobs at Indero | HiringCafe

Intern, Finance / Stagiaire en finance

Finance Intern

Currently pursuing a Bachelor's in accounting/finance/business; basic accounting knowledge, Microsoft Excel familiarity, attention to detail, strong communication in English, discretion with confidential information, ability to work independently and in teams.

Quality Systems Specialist / Spécialiste, Systèmes Qualité, Canada

Quality Systems Specialist

Bachelor's or equivalent, 3+ years QA experience in pharma/clinical research, strong QMS/CAPA/audit skills, knowledge of ICH/GxP/FDA/Health Canada/EU, bilingual French & English, Microsoft Office proficiency, willing to travel 10–30%.

Director, Business development Dermatology & Rheumatology, CRO, Romania

Director Business Development

Bachelor's degree required, Master’s preferred. 5+ years in biotech/pharma/CRO business development or sales, scientific knowledge of clinical research, proven sales track record, strong industry network, and Microsoft Office 365 proficiency.

Director, Business development Dermatology & Rheumatology, CRO, Spain

Director, Business Development

Bachelor's degree required (Master's preferred), 5+ years CRO/pharma/biotech sales or business development experience, scientific knowledge of clinical research, proven sales track record, strong leadership and communication, Microsoft Office 365 proficiency.

Director, Business development, Dermatology & Rheumatology, CRO, Poland

Director of Business Development

Bachelor's degree required, 5+ years CRO/pharma/biotech sales or business development experience, strong sales track record and industry network in dermatology/rheumatology, Microsoft Office 365 proficiency, leadership and negotiation skills.

Business Development Director

Bachelor's degree required, Master’s preferred; 5+ years CRO/pharma/biotech sales or business development experience; proven sales track record; strong leadership, communication, and organizational skills; Microsoft Office 365 proficiency.

Strategist, Operational Strategy (Spain)

Strategist

Defines operational strategy and proposal content for clinical trials; requires B.Sc. or equivalent, dermatology and CRO experience, 5+ years in clinical operations/project management with 2+ years leadership, ICH-GCP knowledge, and strong English communication.

Strategist, Operational Strategy (Poland)

B.Sc. or equivalent, 5+ years in clinical operations/project management (CRO required) with ≥2 years leadership; dermatology experience required; strong knowledge of ICH-GCP and CRO services; excellent English; analytical and stakeholder engagement skills.

Statistical Programmer-Romania

Statistical Programmer

Develop and validate SDTM/ADaM datasets, aCRFs, TLFs; use SAS and Pinnacle 21; 1+ year clinical research/statistical programming experience; Bachelor's in Statistics/Computing or related; knowledge of CDISC and XML.

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

B.Sc. or equivalent experience; 5+ years in clinical operations/project management with 2+ years in leadership; dermatology experience required; strong ICH-GCP knowledge; excellent English; familiarity with tools informing operational strategy.

Technician, Accounts Payables (Argentina)

Accounts Payable Technician

Diploma in accounting, 3 years in a similar role, excellent English, strong MS Office skills (Excel, Word, Outlook), ability to work in fast-paced environment, autonomy and initiative.

Risk Manager (Clinical Research)-Spain

Risk Manager

Bachelor's degree in a relevant field; 3+ years risk management in clinical research and 5+ years across monitoring, data management or drug safety; expertise in GCP/ICH E6 (R3), risk-based monitoring, MS Excel and RACT; fluent English.

Senior Regulatory Affairs Specialist-Germany

Regulatory Affairs Specialist

Bachelor's in a scientific discipline, 3+ years clinical regulatory affairs experience with IRB/IEC/CTA submissions, strong knowledge of global regulatory requirements (EU-CTR, FDA, Health Canada), and fluency in English.

Risk Manager (Clinical Research)-Poland

Bachelor's degree in a clinical research field, 3+ years risk management in clinical research and 5+ years across monitoring/data management/drug safety, GCP/ICH E6 (R3) expertise, Microsoft Excel (pivot tables) and data visualization proficiency, Lean Six Sigma knowledge, fluent English.

Start-Up, Manager, EU, remote: Poland, Spain or Germany

Start-Up Manager

Bachelor's in life sciences, nursing or related (Master's preferred); 3+ years clinical trial start-up experience; ability to lead multi-country start-up activities, strong project management and communication skills.

Risk Manager (Clinical Research)-Canada

Bachelor's in a relevant field; experience in CRO/pharma with minimum 3 years in clinical research risk management and 5 years across monitoring, data management, or drug safety; expertise in GCP/ICH E6 (R3), RBM, Excel, analytical visualization, and Lean Six Sigma.

Senior Regulatory Affairs Specialist-Romania

Bachelor's in a scientific discipline, 3+ years clinical regulatory affairs (IRB/IEC/CTA experience), strong knowledge of global regulatory requirements (EU-CTR, FDA, Health Canada), English fluency, and leadership/mentoring experience.

Sr Talent Acquisition Advisor (contractual) / Conseiller senior acquisition de talents (consultant)

Talent Acquisition Advisor

University degree in HR or related field, 5+ years in in-house recruiting, bilingual English/French, ATS and sourcing experience, MS Office (Excel/Word/Outlook), knowledge of GCP/Health Canada/FDA, strong communication and stakeholder management.

Senior Statistical Programmer-Romania

Bachelor's in statistics/computer science (master's preferred); 5+ years clinical research experience including 4 years statistical programming and 1 year as Lead; strong SAS, CDISC knowledge; XML and Pinnacle 21 experience an asset; must be legally able to work in Romania.

Sr Talent Acquisition Advisor (9-month contract)/ Conseiller.ère senior en acquisition de talents

Bilingual (EN/FR) recruiter with 5+ years in in‑company recruiting, ATS and sourcing experience, university degree preferred, MS Office proficiency, knowledge of pharma/CRO and GCP/Health Canada/FDA an asset.

Senior Project Coordinator-Spain

Project Coordinator

Bachelor's in a relevant field or equivalent experience, minimum 2 years as a project coordinator in clinical research/CRO, site start-up experience, proficiency in Microsoft Word/Excel/PowerPoint and eTMF, English required; French or other languages an asset.

Senior Clinical Research Associate, Dermatology & Rheumatology CRO, Alberta, Canada

Clinical Research Associate

B.Sc. or nursing degree (or equivalent experience); 5+ years of on-site clinical monitoring experience in CRO/pharma/biotech; dermatology and rheumatology exposure; strong ICH/GCP knowledge, English communication, Microsoft Office proficiency, and ability to travel ~65%.

Statistical Programmer-Canada

Bachelor's in statistics/computing, 1+ year clinical research/statistical programming experience, strong SAS skills, knowledge of CDISC/SDTM/ADaM, Pinnacle 21 and XML exposure, strong communication and project skills.

Senior Regulatory Affairs Specialist-Poland

Bachelor's in a scientific discipline, 3+ years clinical regulatory affairs experience, experience with IRB/IEC/CTA submissions, strong knowledge of global regulatory requirements (EU-CTR, FDA, Health Canada), and fluency in English.

Senior Regulatory Affairs Specialist-Spain

Bachelors in a scientific discipline, 3+ years clinical regulatory affairs experience (IRB/IEC/CTA submissions), strong knowledge of global regulatory requirements (EU-CTR, FDA, Health Canada), and fluency in English.

Senior Statistical Programmer-Canada

Bachelor's in statistics or computing, 5+ years clinical research experience including 4 years statistical programming and 1 year as lead; strong SAS and CDISC knowledge, Pinnacle 21 and XML experience; English required, French an asset.

Senior Project Coordinator, EU

Bachelor’s in relevant field or equivalent experience, minimum 2 years as a project coordinator in clinical research/CRO; site start-up experience, proficiency in Microsoft Word/Excel/PowerPoint and eTMF, strong communication and knowledge of GCP/FDA/Health Canada.

Senior Statistical Programmer-Argentina

Bachelor's in statistics/computing (master's preferred), 5+ years clinical research (including 4 years statistical programming and 1 year as Lead), strong SAS and CDISC knowledge, Pinnacle 21 and XML experience, English proficiency; must be eligible to work in Argentina.

Statistical Programmer-Argentina

Bachelor's in Statistics/Computer Science (master's preferred); 1+ year clinical research including statistical programming; strong SAS and CDISC knowledge; experience with SDTM/ADaM, Pinnacle 21, XML; strong communication and attention to detail.

Senior Project Coordinator-Poland

Bachelor's in a relevant field or equivalent experience, minimum 2 years as a project coordinator in clinical research/CRO, site start-up experience, proficiency in English, MS Word/Excel/PowerPoint, knowledge of essential trial documentation and GCP/FDA/Health Canada guidance.

Risk Manager (Clinical Research)-India

Bachelor's degree relevant to clinical research; 3+ years risk management in clinical research and 5+ years across monitoring, data management or drug safety; GCP/ICH E6 (R3) expertise; Excel and data visualization proficiency; strong analytical, communication and leadership skills.

Senior Azure Administrator-Argentina

Azure Administrator

Bachelor's in CS/Info Security, 10+ years cloud security architecture experience (Azure preferred), expertise in Azure security services and IAM, knowledge of compliance frameworks, strong communication and project skills.

Risk Manager (Clinical Research)-Romania

Bachelor's degree in a relevant field; minimum 3 years risk management in clinical research and 5 years across monitoring/data/safety; expertise in GCP/ICH E6 (R3), risk-based monitoring, MS Excel, RACT, Lean Six Sigma, strong analytical and communication skills, fluent English.

Risk Manager (Clinical Research)-USA

Bachelor's degree relevant to clinical research, 3+ years risk management in clinical research and 5+ years across monitoring/data management/drug safety; expertise in risk-based monitoring, GCP/ICH E6 (R3), Microsoft Excel, analytical visualization, Lean Six Sigma and RACT tools.

Clinical Study Builder-Argentina

Clinical Study Builder

B.Sc./M.Sc. in a related field; minimum 2 years Veeva CDMS study build experience; eCRF design and database programming skills; Medrio/Rave experience preferred; strong English communication and project skills.

Biostatistician - Canada

Biostatistician

Master's degree or PhD in Statistics/Biostatistics required; 1+ year clinical trials experience required; CDISC, SAP/TLF experience and SAS knowledge preferred; strong project, communication, and regulatory knowledge (ICH/FDA/Health Canada).

Auditeur, qualité clinique et conformité / Auditor, Clinical Quality and Compliance, Canada

Clinical Quality and Compliance Auditor

Bachelor's or equivalent, 3+ years in pharmaceutical/research clinical quality, strong knowledge of ICH/FDA/Health Canada and EU standards, audit and CAPA expertise, bilingual French/English, Microsoft Office proficiency, willing to travel 10–30%.

Medical Monitor Associate, Dermatology & Rheumatology, Argentina

Medical Monitor Associate

Medical degree and board-certified dermatologist; minimum 1 year clinical research/CRO or pharmaceutical industry experience; proficiency with Microsoft Word, Excel, PowerPoint, EDC and SharePoint; knowledge of GCP and relevant regulatory guidelines.

Clinical Trial Manager II / Gestionnaire d’essais cliniques II, Dermatology & Rheumatology, Canada

Clinical Trial Manager

8+ years clinical research experience with monitoring experience and 2+ years Lead CRA/Team Leader experience; strong ICH/GCP knowledge; Microsoft Office proficiency; fluent English; occasional travel up to 10%.

Clinical Scientist, Dermatology & Rheumatology CRO, Canada

Clinical Scientist

MSc in life sciences (PhD an asset); experience writing clinical/regulatory documents and analyzing study data; strong English writing skills and Good Clinical Practice knowledge; Microsoft Word proficiency.