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.
You will be responsible for the preparation and submission of regulatory documents in compliance with EU CTR and other applicable guidelines. Additionally, you will provide leadership for clinical trial start-up activities and serve as the primary point of contact for sponsors and project teams.
The Site Selection Specialist acts as the primary contact for site identification and feasibility activities within clinical research projects. They manage investigator relationships, coordinate site qualification visits, and track activities within the Clinical Trial Management System.
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 Clinical Trial Manager II is responsible for the operational management and oversight of clinical investigative sites and clinical operations deliverables. This includes training and mentoring CRAs, managing site performance, ensuring adherence to study plans, and maintaining project budgets and timelines.
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 Clinical Research Associate II monitors clinical studies at investigative sites to ensure compliance with protocols, SOPs, and regulatory requirements. They also conduct site visits, perform source data verification, and mentor junior staff to meet study objectives.
The Senior CRA monitors clinical studies at investigative sites or remotely to ensure compliance with protocols, SOPs, and regulatory requirements. They are responsible for site qualification, initiation, monitoring, and close-out visits while maintaining productive relationships with site staff.
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 Clinical Trial Manager II is responsible for the operational management and oversight of clinical investigative sites and monitoring deliverables. They lead monitoring efforts, ensure compliance with SOPs and regulations, and provide mentorship to Clinical Research Associates.
The Clinical Operations Manager oversees a team of clinical staff, ensuring monitoring activities meet sponsor requirements and quality standards. They are responsible for resource allocation, performance management, and driving process improvements through innovation and technology adoption.
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 Senior Clinical Data Manager will oversee the end-to-end data management process for clinical trials, ensuring accuracy, security, and compliance with protocols. Responsibilities include database setup, data cleaning, vendor oversight, and providing regular status reports to clients and project teams.
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 Senior Clinical Data Manager will oversee the end-to-end clinical data management process, including study setup, database maintenance, and reconciliation. They are responsible for leading study teams, managing vendor deliverables, and ensuring data accuracy and compliance with protocol requirements.
The Project Manager oversees the initiation, planning, and execution of clinical research projects while managing study-specific vendors throughout the project lifecycle. They act as the primary contact for sponsors and internal teams, ensuring compliance with budgets, timelines, and regulatory requirements.
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 support for site activation and maintenance throughout the clinical trial lifecycle. They ensure project timelines and quality standards are met while collaborating with internal teams and external 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 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 II leads site activation activities and manages essential regulatory and clinical trial documentation. They act as the primary point of contact for investigator sites and ensure compliance with study timelines and quality standards.
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 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 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 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 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 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.
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.
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 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.
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.
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 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.
