Clinical Project Manager

Job Overview

Accountable for regional study delivery with appropriate inspection readiness quality, within agreed timelines and budget. The Clinical Project Manager leads the regional clinical operations team (including oversight of external partners working on the regional level) and acts as point of escalation for resolution of issues within the region for the assigned study. Ensures alignment of regional deliverables with overall study goals.

Essential Functions

Leads the regional clinical operations team effectively, ensures effective decision making and acts as point of escalation for resolution of issues within the region for the assigned study

Leads external vendors involved in study delivery on a regional level

Collaborates with key stakeholders in the region and provides regular updates on study progress in the region to senior management and Global Clinical Project Manager as required

Represents the regional project team at internal meetings and at the cross-functional Clinical Project Team (CPT) meetings

Leads regional operations meetings with all regional project team members

Leads planning and management of the assigned clinical projects from feasibility through closeout activities for region, in line with global project timelines

Generates, manages, and maintains high quality study start up and recruitment timelines for region and tracks progress towards these

Ensures that the clinical study is operationally feasible in the region, drives trial feasibility, country allocation and site selection process for assigned region in collaboration with feasibility managers, country heads, medical affairs and any other stakeholders

Provides regional input on global study plans as required

Ensures timely availability of local adaptations of global study documents such as informed consent forms, in close collaboration with other key stake holders to ensure timely submission to regulatory authorities and ECs/IRBs

Accountable for submissions of study in countries in assigned region in close collaboration with regional study start up team and regulatory affairs

Ensures regional and country information in study systems and tools is entered and up to date

Collaborates closely with CRAs in the region to ensure proper study execution at the sites. Reviews and signs-off monitoring reports

Responsible for working with regional and country teams to ensure that country and site level Trial Master File is created, maintained and QC’d on a regular basis as per the study TMF QC plan

Provides input to Global Clinical Supplies regarding drug inventories in region and reviews local drug labels for region. Provides input on local regulatory approval and reimbursement status of comparator drugs used in study for countries in region

Manages the trial data collection process for the region, drives data entry and query resolution

As required, supports planning and execution of the Clinical Study Report in collaboration with Global Clinical Project Manager and Medical Writing

Handles escalated issues or problems with the sites in region in close collaboration with stakeholders such as country heads

Monitors study activities in region to ensure compliance with the study protocol, SOPs, ICH/GCP and all other relevant regulations

Ensures inspection readiness for study in region at any point in time throughout the study life cycle

Informs Global Clinical Project Manager of any issues arising on the study, evaluates impact and ensures solutions are implemented

Prepares sites for quality assurance audits and inspections, drives responses to audit and inspection findings as appropriate

Collaborates with CPT members and colleagues to ensure cross-team, site learnings, and best practices are shared

Leads improvements and partners with CPT members to enhance the efficiency and the quality of the work performed on assigned studies

Contributes to development, optimization and review of work instructions and SOPs as required

Works with the sourcing team to select and manage regional study vendors

Manages regional study budgets

Works closely with Clinical Business Operation on investigator fees, site payment issues and patient travel reimbursement activities

Identifies and manages regional team resource needs and establishes contingency plans for key resources

Monitors regional resource utilization over study life cycle and liaises with functional managers as needed

Qualifications

Bachelor's Degree Life sciences or related field

Progressive experience in clinical research within biotech, pharma or CRO industry

7 years of monitoring experience including > 1 years project management experience or equivalent combination of education, training and experience.

Advanced knowledge of job area, and broad knowledge of other related job areas, typically obtained through advanced education combined with experience.

Knowledge of clinical trials - Knowledge of clinical trial conduct, and skill in applying applicable clinical research regulatory requirements i.e. ICH GCP and relevant local laws, regulations and guidelines, towards clinical trial conduct. Broad protocol knowledge; therapeutic knowledge desired.

Communication - Strong written and verbal communication skills including good command of English language. Strong presentation skills.

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.