Associate Director, Clinical Trials Materials Position Available In Cobb, Georgia

Tallo's Job Summary: We are seeking an Associate Director, Clinical Trials Materials to join IQVIA Laboratories in Marietta, GA. As the Associate Director, you will direct operational actions, planning, development, and implementation of clinical trials materials processes and procedures. Responsibilities include providing regulatory expertise, guidance, and strategic direction to staff, internal, and external customers. A Bachelor's Degree and 6 years of relevant experience, including 3 years in a leadership capacity, are required for this role. The potential base pay range for this position is $107,500.00 - $199,700.00. Join us at IQVIA Laboratories and help make the extraordinary possible!

Company:
IQVIA
Salary:
$153600
JobFull-timeOnsite

Job Description

Associate Director, Clinical Trials Materials Associate Director, Clinical Trials Materials
locations
Marietta, Georgia, United States of America
time type
Full time
posted on
Posted 30+ Days Ago
job requisition id

R1454035

We are seeking an Associate Director, Clinical Trials Materials to join IQVIA Laboratories in Marietta, GA.
We hire passionate innovators who drive healthcare forward through thoughtful and inclusive collaboration. If you want to discover a career with greater purpose, join us as we transform and accelerate research and development.
As the Associate Director, Clinical Trials Materials, you will direct operational actions, planning, development, and implementation of clinical trials materials processes and procedures. You will provide regulatory expertise, guidance, and strategic direction to staff, internal, and external customers.
What you’ll be doing:
Supporting strategic direction for global clinical trials materials.
Executing strategic initiatives in a timely manner in accordance with the project plan.
Managing allocation of clinical trials materials resources, including project initiatives and assignments.
Providing operational liaison between departments as needed.
Planning, coordinating, and providing leadership for clinical trials materials projects and initiatives.
Developing and maintainingmunication and collaboration with internal and external clients, regulatory agencies, couriers, and relatedpanies.
Maintaining and adhering to standard operating procedures (SOPs) related to clinical trials materials, regulations, and training.
Serving as a regulatory consultant for internal and external clients and global IQVIA laboratories.
What we are looking for:
Bachelor’s Degree.
6 years of relevant experience, including 3 years experience in a leadership capacity.
Comprehensive knowledge of clinical trials materials procedures.
Effective organizational and interpersonal skills.
Other equivalentbination of education, training, and experience may be accepted in lieu of degree.
The knowledge, skills, and abilities needed for this role:
Ability to lift up to 50 lbs., frequent standing and walking, occasional sitting, close eye work requirement puter, typing, reading small s). Physical demands vary depending on the assigned work area and work tasks. Occasional exposure to cold temperatures.
Effectivemunication skills and strong presentation skills.
Ability to lead and motivate high-performing teams.
Strong organizational and problem-solving skills.
What we offer you:
We put our employees at the center of everything we do and aremitted to providing them, and their families, with benefits that meet their diverse and changing needs. We invest in integrated benefits programs and resources to take care of our employees’ physical, mental, emotional, financial, and social well-being so they can thrive at home and at work, at any stage of their well-being journey.
To learn more about our benefits, visit /benefits.
If you’re looking to unleash your potential, join IQVIA Laboratories to help make the extraordinary possible!
IQVIA is a leading global provider of clinical research services,mercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development andmercialization of innovative medical treatments to help improve patient oues and population health worldwide. IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. /eoe
The potential base pay range for this role, when annualized, is $107,500.00 – $199,700.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms ofpensation may be offered, in addition to a range of health and welfare and/or other benefits.
About Us
IQVIA is a leading global provider of clinical research services,mercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development andmercialization of innovative medical treatments. Everything we do is part of a journey to improve patient oues and population health worldwide.
To get t, we seek out diverse talent with curious minds and a relentlessmitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our d goal of helping customers improve the lives of patients everyw. Thank you for your interest in growing your career with us.

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