• Director , Clinical Research Operations Jobs in United States Of America - 25368131

  • Iqvia
  • United States Of America, Usa
  • Save Job
  • 10 - 13 Years
  • Posted : above 1 month

Job Description:

Join us on our exciting journey! IQVIA is The Human Data Science Company, focused on using data and science to help healthcare clients find better solutions for their patients Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness advances in healthcare information, technology, analytics and human ingenuity to drive healthcare forward


This person is responsible for coordinating clinical studies and will lead the Clinical Team to achieve seamless management and execution of clinical trials The Director of Clinical Operations will develop and implement clinical operations strategies, leading the execution of clinical trials, in collaboration with the Medical Director This person will oversee coordination and management of the clinical studies As Director of Clinical Operations, this person will work closely with the other directors on the clinical sections of Companys work plans, funding applications and regulatory submissions

Qualification Requirements

Education Masters degree or MPH is required Other equivalent or higher degrees are accepted

Experience at least 10 years of experience in clinical research with supervisory experience, regardless of when last degree was obtained

Language skills / other skills / mathematical skills no change from current job description

Essential Duties and Responsibilities

Clinical Operations Oversee planning, implementation, and reporting of clinical trials

Set strategy for effective operational management of clinical trials
Ensure clinical studies meet milestones and timelines
Improve efficiencies within clinical operations, including oversight of SOPs and implementation of risk evaluation and mitigation processes for clinical studies
Ensure clinical studies are properly resourced, managed and executed within budget
Participate in the design, development and review of clinical trial protocols, amendments, informed consent forms, study guides, case report forms, and any other clinical research related documents and study reports
Identify study sites and investigators for clinical studies with Medical Director
Oversee planning for investigator meetings and ensure studies are monitored to industry standards including travel to sites when necessary
Work with Product Development group to oversee packaging, labelling, and distribution of study drug supply from manufacturer to study sites
Participate as required in the preparation of the clinical contribution to IND and IDEs, Investigational Brochure, regulatory Briefing Documents, and other relevant documentation for submission to FDA and other regulatory authorities
Oversee electronic and paper file management, including maintenance and archiving of Trial Master Files and other clinical trial documents in compliance with applicable guidelines and regulations
Accountable for conduct of clinical trials in compliance with GCP and all relevant regulations, policies, and ethical standards

Contract Management Responsible for overall oversight of sub-agreements and contracts in support of clinical trials

Responsible for workscope development, vendor selection, negotiations, and oversight for collaborations and services such as data management/statistical analysis, laboratory analysis
Technical monitor on multiple and diverse funding agreements

Funded Program Management As member of Senior Management Team, work to facilitate communication with and reporting to project funders

Participate in work plan development and monitoring
Prepare routine reports (semi-annual and/or annual) for funders
Prepare presentations and participate in meetings as needed to update funders and discuss program status

Proposal Development Collaborate with Senior Management Team to develop and submit proposals for funding

Provide input on study design and budget development
Support resource allocation


Lead team of 5 to 8 people, including Project Managers, Clinical Research Associates, and support staff
Provide mentorship to direct reports and maintain clear communication on performance
Build and maintain positive team-based culture

Education / Experience

Masters degree, advanced training in a scientific or a health care field preferred
Excellent knowledge of clinical study conduct
Experience managing all phases of clinical trials
Experience being a member of cross-functional team
Experience in managing vendors preferred
Experience developing and monitoring clinical study budgets


Strong management skills

Effective process and project management skills

Solution oriented

Outstanding written and verbal communication skills

Expert knowledge of clinical study conduct

Ability to multi-task

IQVIA is an EEO Employer - Minorities/Females/Protected Veterans/Disabled

We know that meaningful results require not only the right approach but also the right people Regardless of your role, we invite you to reimagine healthcare with us You will have the opportunity to play an important part in helping our clients drive healthcare forward and ultimately improve human health outcomes Whatever your career goals, we are here to ensure you get there! We invite you to join IQVIA

Job ID R1068248

Profile Summary:

Employment Type : Full Time
Eligibility : Any Graduate
Industry : Consulting Services
Functional Area : Bio Tech/R&D/Scientist
Role : Clinical Research
Salary : As per Industry Standards
Deadline : 09th Jun 2020

Key Skills:

These are some of our most popular tutorials

People who search this job also searched for the following Keywords

Salary trends based on over 1 crore profiles

View Salaries

All rights reserved © 2018 Wisdom IT Services India Pvt. Ltd DMCA.com Protection Status