Jobs at Indero | HiringCafe

Project Manager (Argentina)

Project Manager

B.Sc. preferred; 3+ years in clinical study project roles (2+ years coordinating trial activities); strong knowledge of GCP/ICH/FDA/Canadian regs, Microsoft Office, English required, French an asset, project management and people management experience.

Project Manager (Romania)

B.Sc. in related field, 3+ years in similar clinical study roles, 2+ years coordinating clinical trial activities, strong knowledge of GCP/ICH/FDA regulations, Microsoft Office proficiency, English required; French is an asset.

Clinical Operations Manager, Gestionnaire des opérations cliniques, North America, Remote

Clinical Operations Manager

Bachelor's degree in a relevant field, minimum 6 years clinical research experience (4 years as Sr. CRA or 2 years as Project Manager/CTM), strong monitoring and quality experience, Microsoft Office proficiency, experience with AI tools, travel up to 20%.

Clinical Trial Manager II, US, remote

Clinical Trial Manager

8+ years clinical research experience including monitoring, 2+ years in Lead CRA/Clinical Team Leader role, B.Sc. or nursing degree or equivalent experience preferred, strong ICH/GCP knowledge, Microsoft Office proficiency, leadership and problem-solving skills.

Project Manager (Germany)

3+ years in clinical study/project roles, 2+ years coordinating clinical trial activities; B.Sc. preferred; strong GCP/ICH knowledge, Microsoft Office proficiency, project management and people management skills; English required.

Regulatory Affairs Specialist-Romania

Regulatory Affairs Specialist

Bachelor's degree in a scientific discipline, 2+ years clinical research regulatory experience in Romania, experience preparing/submitting CTAs, CTIS experience preferred, strong knowledge of EU regulatory guidelines, GCP/ICH, and fluent English.

Line Manager, Regulatory Affairs, Canada, remote

Regulatory Affairs Manager

Bachelor's in a scientific discipline, 3+ years regulatory affairs experience in pharma/biotech/CRO with IRB/IEC and CTA submissions, CTIS knowledge, Microsoft Office proficiency, English fluency; functional staff management experience an asset.

Clinical Study Builder-Canada

Clinical Study Builder

B.Sc. or M.Sc.; minimum 2 years Veeva CDMS study build experience; Veeva Study Builder certification and Medidata Rave/Medrio experience preferred; knowledge of CRF design, GCP/ICH, strong English communication and multitasking.

Project Manager II (Romania)

B.Sc. in a related field; 5+ years industry experience with minimum 3 years managing Phase I-III trials; experience with dermatology/rheumatology and multi-site trials > $3M; strong GCP/ICH knowledge, Microsoft Office, and English communication.

Project Manager II (Germany)

B.Sc. in clinical research, 5+ years industry experience, 3+ years Phase I-III project management, experience with dermatology/rheumatology multi-site trials > $3M, knowledge of GCP/ICH/FDA/Canadian regs, Microsoft Office, English.

Administrateur Azure principal/Senior Azure Administrator-Canada

Azure Administrator

Bachelor's in CS/InfoSec, 10+ years cloud security architecture experience (Azure preferred), expertise with Azure security services, IAM/Azure AD, compliance frameworks, project management; preferred Azure security certifications.

Project Manager (Spain)

B.Sc. in a related field, 3+ years in similar clinical study/project roles (2+ years coordinating trial management), strong knowledge of GCP/ICH/FDA/Canadian regs, Microsoft Office proficiency, English required, project and people management skills.

Director Business Development, East coast, United States

Business Development Director

5+ years experience in biotech/pharma/CRO business development or sales, bachelor’s degree required (master’s preferred), strong clinical research knowledge, proven sales track record, leadership and MS Office 365 proficiency.

Project Coordinator I-Argentina

Project Coordinator

Entry-level support for clinical study documentation and site activation; college/bachelor's degree preferred, English proficiency, Microsoft Office skills, attention to detail, knowledge of GCP/SOPs, CTMS/eTMF experience a plus.

Project Coordinator II (Argentina)

Bachelor's degree or equivalent experience; 1-2 years clinical research experience (CRO/biotech/pharma preferred); knowledge of GCP/ICH and FDA/Health Canada guidelines; strong English communication and organizational skills.

Regulatory Affairs Associate-Romania

Regulatory Affairs Associate

Bachelor's in a scientific discipline, 0-2 years clinical regulatory affairs experience; IRB/IEC or CTA submission experience preferred; Microsoft Office proficiency; English fluency; strong attention to detail and organizational skills.

Medical Monitor, Rheumatology, Canada or Argentina

Medical Monitor

Medical degree required; minimum 2 years relevant clinical research/CRO experience (medical monitoring, medical affairs, safety); rheumatology experience preferred; strong knowledge of drug development and GCP; ability to provide 24/7 on-call medical support.

Biostatistician - Argentina

Biostatistician

Master's or PhD in statistics/biostatistics required, 1+ year clinical trials experience, knowledge of ICH and clinical trial processes, CDISC/SAS experience preferred, strong English communication; French is an asset.

Regulatory Affairs Associate-Poland

Bachelor's in a scientific discipline, 0-2 years clinical regulatory affairs experience, experience preparing IRB/IEC or CTA submissions preferred, Microsoft Office (Word, Excel, Outlook) proficiency, fluent English, strong attention to detail and organizational skills.

AI Transformation Lead, Argentina, remote

AI Transformation

5+ years in similar role, CRO experience preferred; hands-on deployment of M365 Copilot, Copilot Studio and Power Platform; strong stakeholder engagement, AI governance, and workshop facilitation skills; bachelor’s degree preferred.

Regulatory Affairs Specialist-Poland

Bachelor's in a scientific discipline, 2+ years clinical research/regulatory experience in Poland, experience with CTA/CTIS desirable, strong knowledge of EU CTR, GCP/ICH, fluent English, document preparation and submission expertise.

Project Manager (Poland)

B.Sc. preferred; 3+ years in similar clinical research role (2+ years coordinating clinical trial activities). Strong knowledge of GCP/ICH/FDA/Canadian regulations, Microsoft Office, project management competencies, and excellent communication skills (English required, French asset).

Project Manager II / Gestionnaire de projet II (Canada)

B.Sc. in clinical research field, 5+ years industry experience with minimum 3 years managing Phase I-III clinical trials, experience with dermatology/rheumatology and multi-site trials >$3M, strong GCP/ICH/FDA knowledge, Microsoft Office proficiency, English required.

Business Applications Analyst, Argentina, remote,

Business Applications Analyst

Bachelor's degree in related field, 3+ years with enterprise systems (ERP/HRMS/CRM), experience gathering requirements, configuring enterprise applications, functional analysis; Infor FSM, Salesforce, Bob are assets.

Risk Manager (Clinical Research)-Argentina

Risk Manager

Bachelor's in a clinical-research field, 3+ years in clinical research risk management (5+ years across monitoring/data/drug safety preferred), GCP/ICH E6 (R3) expertise, Microsoft Excel and RACT tool proficiency, strong analytical and communication skills, fluent English.

Future opportunities/Opportunités de carrière

Future Opportunities

Express interest in future roles; must be legally able to work in Canada. Opportunities include career advancement, collaborative environment, and learning; remote candidates in Canada and internationally may be considered.

Project Manager II (Spain)

B.Sc. in related field; 5+ years industry experience with minimum 3 years in Phase I-III project management; experience with dermatology/rheumatology trials and managing budgets > $3M; GCP/ICH/FDA knowledge; Microsoft Office; English required, French an asset.

Future opportunities / Opportunités de carrière

Open talent pool for future roles; candidates must be legally able to work in Canada. Company offers career advancement, collaborative environment, learning opportunities, and accommodations for applicants with disabilities.

Project Manager II (Argentina)

B.Sc. in a related field, 5+ years industry experience with at least 3 years in Phase I-III clinical trial project management; experience with dermatology/rheumatology and multi-site trials; strong GCP/ICH knowledge, Microsoft Office, and English communication skills.

Clinical Study Builder-India

2+ years Veeva CDMS study build experience, B.Sc. or M.Sc. in a related field, eCRF/CRF design and build, familiarity with Medrio/Medidata Rave, strong English communication, ability to lead multiple study builds.

Administrative Assistant / Assistant(e) administrative

Administrative Assistant

Secondary school diploma or vocational studies; reception/administrative experience an asset; bilingual French and English; intermediate Microsoft Office (Word, Excel, PowerPoint); strong communication, attention to detail, multitasking, and customer-service skills; legal authorization to work in Canada.

Biostatistician - Romania

Master's or PhD in Statistics/Biostatistics or related, 1+ year clinical trials experience in biotech/pharma/CRO, knowledge of ICH and regulatory guidance, CDISC standards and SAS experience preferred, strong communication and project skills.

Clinical Study Builder-Romania

2+ years Veeva CDMS study build experience; BSc/MSc in related field; proficiency with Veeva CDMS, Medrio/Rave; CRF design and programming knowledge; English proficiency; ability to lead multiple study builds.

Project Coordinator II-Canada

Bachelor's degree or equivalent experience, 1+ year clinical research experience, knowledge of GCP/ICH, CTMS/eTMF experience preferred, strong communication and organizational skills; English required.

Project Manager II (Poland)

B.Sc. in clinical research or related field; 5+ years industry experience with minimum 3 years in Phase I-III trial project management; experience with dermatology/rheumatology trials and managing >$3M budgets; strong GCP/ICH knowledge and MS Office skills; English required.