Associate Director, Clinical Trials Materials

IQVIA Argentina; Marietta (GA); On-site; USD 107,000 - 200,000; Full time

Job summary

An established industry player is seeking an Associate Director for Clinical Trials Materials. This role involves directing operational actions and providing regulatory expertise while leading high-performing teams. The ideal candidate will have a strong background in clinical trials materials and effective communication skills. Join a forward-thinking organization committed to transforming healthcare through collaboration and innovation, where your contributions can significantly impact patient outcomes and the development of groundbreaking medical treatments.

Qualifications

• 6 years of relevant experience, including 3 years in a leadership role.
• Comprehensive knowledge of clinical trials materials procedures.

Responsibilities

• Direct operational actions and planning for clinical trials materials.
• Provide regulatory expertise and strategic direction to staff.

Skills

Leadership

Communication Skills

Problem-Solving Skills

Organizational Skills

Regulatory Knowledge

Education

Bachelor's Degree

Job description

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 maintaining communication and collaboration with internal and external clients, regulatory agencies, couriers, and related companies.
• 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 equivalent combination 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 (computer, typing, reading small prints). Physical demands vary depending on the assigned work area and work tasks. Occasional exposure to cold temperatures.
• Effective communication 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 are committed 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 https://jobs.iqvia.com/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, 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 athttps://jobs.iqvia.com

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. https://jobs.iqvia.com/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 of compensation may be offered, in addition to a range of health and welfare and/or other benefits.