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.
The Project Manager II 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 coordinating operational activities across various departments.
The Clinical Data Manager will lead and manage clinical studies, ensuring data is collected, managed, and reported accurately and securely. They are responsible for developing eCRF specifications, conducting database validation, and overseeing data management documentation throughout the study lifecycle.
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 Clinical Trial Manager II is responsible for the operational management and oversight of clinical investigative sites and monitoring deliverables for early-phase trials. They also manage project timelines, budgets, and resources while ensuring compliance with regulatory standards and study-specific requirements.
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 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 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 Senior Clinical Data Manager leads multiple clinical studies, ensuring accurate data collection, management, and reporting in compliance with regulatory requirements. They are responsible for EDC system development, vendor oversight, data cleaning, and mentoring junior team members.
The Senior Clinical Data Manager will lead and manage multiple clinical studies, ensuring data accuracy, security, and regulatory compliance. Responsibilities include overseeing EDC system development, managing vendor relationships, and performing ongoing data cleaning and reconciliation.
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 service delivery. They lead a team of support personnel while driving continuous improvement, automation, and compliance with 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.
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 delivery.
Oversee Ethics Committee and Regulatory Authority submissions to ensure compliance with regulations and contractual timelines. Provide line management for direct reports, including resource allocation, mentoring, and professional development.
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 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.
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.
The Accounts Receivable Team Lead manages the AR team, oversees invoicing and collections, and maintains KPIs for stakeholders. They are responsible for ensuring operational efficiency, accuracy in billing, and continuous improvement of AR processes.
The Team Lead manages the accounts receivable process, including KPI tracking, invoicing, and collections while overseeing the AR team's workload. They are responsible for maintaining accurate customer profiles, ensuring compliance, and driving continuous improvement in AR tools and processes.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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 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 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.
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 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.
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 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.
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.
