The senior clinical scientist is responsible for authoring and reviewing clinical and regulatory documents, including study protocols, statistical analysis plans, and clinical study reports. They also provide scientific expertise during study conduct, mentor junior staff, and support business development initiatives.
The Principal Central Monitor leads the development of tools and analyses for centralized statistical review to proactively identify and manage study risks. They act as a strategic lead across multiple studies, mentoring junior staff and ensuring monitoring approaches align with study data and processes.
The Principal Central Monitor leads the development of tools, guidelines, and analyses for centralized statistical review of clinical study data. They act as a strategic lead to identify, communicate, and manage risks at the study, country, and site levels throughout the study lifecycle.
The Legal Specialist supports the Legal Department by managing clinical research contracts, ensuring regulatory compliance, and maintaining legal documentation. They also coordinate contract execution workflows and liaise with internal stakeholders and external counsel to provide timely legal support.
The Legal Specialist supports the Legal Department by managing clinical research contracts, ensuring regulatory compliance, and maintaining legal documentation. They also coordinate contract execution workflows and provide administrative support for privacy assessments and internal legal inquiries.
The Legal Specialist supports the Legal Department by managing clinical research contracts, ensuring regulatory compliance, and maintaining documentation systems. They also coordinate with internal stakeholders and external counsel to facilitate efficient legal and administrative operations.
The Clinical Trial Manager oversees clinical investigative sites and manages operational deliverables to ensure trials meet quality, budget, and timeline requirements. They provide leadership to clinical research associates, conduct risk assessments, and serve as the primary point of contact for sponsors.
Lead complex, high-risk validation initiatives across the lifecycle of GxP computerized systems, including strategy, risk assessment, documentation, execution, and release or retirement. Provide technical oversight, coordinate project schedules and stakeholders, mentor analysts, and support audits, inspections, and continuous improvement of CSV practices.
The Vice President of Medical Affairs will provide unified leadership for Medical Monitoring and Pharmacovigilance functions, overseeing strategy, P&L, and regulatory compliance. The role involves driving business development, managing client relationships, and advising the Chief Medical & Scientific Officer on medical and safety risks.
The Medical Monitor provides medical and scientific support to clinical research programs, ensuring data integrity and subject safety oversight. They act as the primary medical contact for investigators and project teams, managing safety reporting and protocol-related medical inquiries.
The Clinical Data Manager is responsible for the development, maintenance, and validation of clinical databases and eCRF specifications. They also oversee data cleaning, reconciliation, and vendor management to ensure compliance with regulatory requirements and study timelines.
The Clinical Study Builder designs and develops electronic case report forms (eCRFs), visit schedules, and data quality checks for medical research studies. They also provide technical support, conduct end-user training, and collaborate with data management teams to ensure compliance with regulatory requirements.
The Clinical Data Coder is responsible for accurately coding medical terms and medications using industry standards like MedDRA and WHO Drug. They also participate in data management activities, including dictionary up-versioning, data review, and resolving data clarifications to ensure accuracy and regulatory compliance.
The Regulatory Project Assistant provides administrative support for regulatory and eTMF operations, including managing documentation in the CTIS portal. They are responsible for tracking project timelines, preparing regulatory submissions, and maintaining trackers for clinical studies.
The Senior Statistical Programmer will lead clinical trials by developing and validating SDTM and ADaM datasets, TLFs, and submission packages. They will also collaborate with biostatistical teams to ensure deliverables meet quality standards and regulatory requirements.
The Senior Statistical Programmer will lead clinical trials by developing and validating SDTM and ADaM datasets, TLFs, and submission packages. They will also collaborate with biostatistical teams to ensure deliverables meet regulatory standards and internal SOPs.
The Senior Statistical Programmer will lead clinical trials by developing and validating SDTM and ADaM datasets, TLFs, and submission packages. They will also collaborate with biostatistical teams to ensure deliverables meet regulatory standards and internal SOPs.
The Project Manager oversees the initiation, planning, and execution of early-phase clinical research projects while managing investigative sites and monitoring deliverables. They ensure compliance with study budgets, timelines, and regulatory requirements while serving as a primary contact for sponsors and internal teams.
The CRA will conduct site qualification, initiation, monitoring, and close-out visits while ensuring clinical trials comply with protocols and regulatory standards. They are responsible for building productive relationships with site staff and performing source data verification to ensure data integrity.
The Biostatistician will act as a lead or support on phase 1 to 4 clinical trials, overseeing statistical protocols, analysis plans, and data management documentation. They will also manage project budgets, timelines, and collaborate with cross-functional teams to ensure compliance with regulatory standards.
You will be responsible for the preparation and submission of regulatory documents and CTA packages to ensure compliance with EU CTR and other regional guidelines. Additionally, you will provide leadership for clinical trial start-up activities and serve as the primary point of contact for sponsors and subcontractors.
The Senior Project Manager serves as the primary point of contact for sponsors, overseeing all phases of clinical trials from start-up to closure. They are responsible for managing project budgets, timelines, vendor deliverables, and leading cross-functional teams to ensure studies are audit-ready.
The Site Selection Specialist acts as the primary contact for site identification and feasibility activities to support clinical research projects. They are responsible for building relationships with investigators, managing feasibility questionnaires, and tracking site selection progress within the Clinical Trial Management System.
The Clinical Data Coder is responsible for performing accurate coding of medical terms and medications using industry-standard dictionaries like MedDRA and WHO Drug. They also oversee coding module setups, manage coding conventions, and coordinate coding activities across multiple clinical studies.
The Senior Clinical Data Coder leads and oversees clinical data coding activities, including module setup, convention management, and dictionary up-versioning. They also provide mentorship to junior staff and ensure all coding processes align with regulatory requirements and sponsor timelines.
The Site Selection Specialist acts as the primary contact for site identification and feasibility activities within clinical research projects. They are responsible for building relationships with investigators, managing feasibility questionnaires, and tracking site selection progress in the CTMS.
The Site Selection Specialist acts as the primary contact for site identification and feasibility activities within clinical research projects. They are responsible for building relationships with investigators, managing feasibility questionnaires, and coordinating site qualification visits to ensure study success.
The Site Selection Specialist acts as the primary contact for site identification and feasibility activities to support clinical research projects. They are responsible for building relationships with investigators, managing feasibility questionnaires, and coordinating site qualification visits.
The Start-Up Manager oversees the end-to-end clinical trial site activation process, including regulatory submissions, site selection, and contracting. They lead cross-functional teams to ensure study timelines are met while serving as the primary point of contact for internal teams and sponsors.
The Project Manager oversees the end-to-end lifecycle of clinical trials, ensuring compliance with budgets, timelines, and regulatory standards. They act as the primary point of contact for sponsors and internal teams while managing operational activities, vendor relationships, and site performance.
The Talent Acquisition Advisor acts as a business partner to hiring managers to manage the full-cycle recruitment process and develop effective sourcing strategies. They are responsible for ensuring a positive candidate experience, maintaining recruitment systems, and supporting employer branding initiatives.
The Talent Acquisition Advisor manages the full-cycle recruitment process and acts as a business partner to hiring managers to identify and attract top talent. They are responsible for developing sourcing strategies, maintaining recruitment systems, and supporting employer branding initiatives.
The Project Director oversees a portfolio of clinical studies, managing project managers and ensuring adherence to quality standards and regulatory requirements. They also lead operational contributions to business development, proposal pricing, and client satisfaction.
The TMF Document Coordinator II manages and performs quality control on clinical trial documentation to ensure compliance with regulatory standards and study-specific guidelines. They also independently lead TMF activities for Investigator-Initiated Studies and smaller sponsored projects, including oversight of the eTMF from start to closeout.
The Project Coordinator provides administrative and coordinating support for site activation activities and ensures clinical trial deliverables meet quality and timeline expectations. They act as a primary point of contact for clinical sites, manage essential regulatory documentation, and assist with study-specific systems and project tracking.
The Senior Project Coordinator provides administrative and coordinating support for site activation activities and ensures that clinical trial deliverables meet internal and external expectations. They manage site start-up timelines, review essential regulatory documents, and act as a primary point of contact for clinical sites.
The Project Coordinator provides administrative and coordinating support for site activation activities and ensures deliverables meet study timelines and quality standards. They act as a primary contact for clinical sites, manage essential regulatory documentation, and assist with project tracking and reporting.
The Clinical Trial Manager II oversees clinical investigative sites and monitoring deliverables to ensure quality and regulatory compliance. They are responsible for mentoring CRAs, identifying site performance trends, and developing action plans to meet study timelines.
The Project Manager oversees the initiation, planning, execution, and closure of clinical research projects while ensuring compliance with budgets, timelines, and regulatory standards. They coordinate tasks between departments, manage stakeholder expectations, and supervise site activation activities.
The Project Director oversees a portfolio of clinical studies and manages the Project Managers responsible for their execution. They are also responsible for business development activities, client satisfaction, and ensuring all studies adhere to regulatory and quality standards.
The Project Director oversees a portfolio of clinical studies and manages project managers to ensure operational excellence and client satisfaction. They are responsible for financial oversight, risk mitigation, and driving business development activities while maintaining compliance with regulatory standards.
This is a general talent pool posting for future career opportunities at Indero. Interested candidates are invited to submit their interest to be considered for upcoming roles.
The Project Manager oversees the end-to-end lifecycle of clinical trials, ensuring compliance with budgets, timelines, and regulatory standards. They act as the primary point of contact for sponsors and internal teams while managing operational aspects such as site activation, vendor coordination, and risk mitigation.
The Project Manager II is responsible for the end-to-end initiation, planning, execution, and closure of clinical trials while ensuring compliance with budgets, timelines, and regulatory standards. They act as the primary point of contact for sponsors and internal teams, overseeing operational activities, vendor management, and risk mitigation throughout the study lifecycle.
The Project Manager oversees the end-to-end lifecycle of clinical trials, ensuring compliance with budgets, timelines, and regulatory standards. They act as the primary point of contact for sponsors and internal teams while managing operational activities, vendor relationships, and site performance.
The Project Manager oversees the end-to-end lifecycle of clinical trials, ensuring compliance with budgets, timelines, and regulatory standards. They act as the primary point of contact for sponsors and internal teams while managing operational activities and site performance.
The Project Manager II is responsible for the end-to-end management of clinical trials, including planning, execution, monitoring, and closure. They act as the primary contact for sponsors and coordinate cross-functional teams to ensure compliance with budgets, timelines, and regulatory standards.
The IT Support Services Manager oversees daily Service Desk operations, endpoint management, and vendor relationships to ensure high-quality IT support. They are responsible for driving continuous improvement, managing IT support personnel, and ensuring compliance with security and regulatory standards.
The Senior Clinical Analyst and Programmer will lead programming activities for data review, safety listings, and centralized monitoring reports. They are responsible for gathering requirements from DM and RBSM departments and creating SAS code to meet these needs within budget and timelines.
Oversees the initiation, planning, and execution of early phase and translational clinical trials, ensuring they are audit-ready and within budget. Acts as the primary point of contact for sponsors and vendors while mentoring other project managers.
Serve as the primary contact for sponsors to oversee the planning, execution, and closure of global clinical trials. Manage project budgets, timelines, and cross-functional teams to ensure deliverables are audit-ready and meet quality standards.
Lead the planning and execution of global clinical trials in dermatology and rheumatology, serving as the primary contact for sponsors. Manage project budgets, timelines, and cross-functional teams to ensure deliverables are audit-ready and completed on time.
Serve as the primary contact for sponsors to lead the planning, execution, and delivery of multi-site clinical trials. Manage project budgets, timelines, and cross-functional teams to ensure studies are audit-ready and meet all objectives.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
