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Senior Clinical Research Associate (Lead CRA)

IQVIA

Senior Clinical Research Associate (Lead CRA)

IQVIA

2 Locations

·

On-site

·

Full-time

·

1w ago

Required Skills

Clinical research monitoring

Data management

Project coordination

The Lead CRAs will be assigned as CRA to one study site as a minimum to verify an adequate understanding of sponsor requirements, procedures, and systems. Thus, requiring the CRA to have more than 4 years of onsite monitoring experience.

The main responsibilities of the Lead CRA are:

  • To oversee the overall study monitoring plan compliance for the studies and countries assigned.

  • To serve as the primary point of contact for IQVIA CRAs and sponsor LSADs for any study monitoring-related questions or concerns.

  • To provide oversight of site monitoring data management activities (entails pulling data management reports and leading the follow-up on missing pages, outstanding queries, etc.).

  • To review Monitoring Visit Reports and advise CRAs on any study-related questions. Initially, 100% MVR review is expected, moving in the future to a risk-based approach after consultation and agreement with sponsor Project Manager.

  • To prepare, lead, and follow up on regular meetings (frequency to be determined by the Project Manager and Lead CRA for each of the studies) with the IQVIA CRA and sponsor Project Manager to review study status, risks, trends, upcoming data timelines, etc.

  • To collaborate and liaise with sponsor Project Manager for project execution support as appropriate.

  • To support CRA with study issue resolution.

  • To report any staff performance concerns to the CRA's manager.

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.

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About IQVIA

IQVIA

IQVIA

Public

Focused on health information technology and clinical research.

10,001+

Employees

Durham

Headquarters

$17B

Valuation

Reviews

3.9

2 reviews

Work Life Balance

2.5

Compensation

2.0

Culture

2.8

Career

3.0

Management

2.5

65%

Recommend to a Friend

Pros

Structured feedback and development process

Meaningful contribution to client businesses

Problem-solving with specialized knowledge

Cons

Strict performance requirements and termination risk

High-level rubric definitions lack detail

No performance bonuses offered

Salary Ranges

42 data points

Junior/L3

Senior/L5

Junior/L3 · Analyst

2 reports

$107,910

total / year

Base

$93,834

Stock

-

Bonus

-

$97,750

$118,068

Interview Experience

3 interviews

Difficulty

3.0

/ 5

Duration

14-28 weeks

Experience

Positive 0%

Neutral 33%

Negative 67%

Interview Process

1

Application Review

2

HR Screen

3

Hiring Manager Interview

4

Technical Manager Interview

5

Executive/GM Interview

6

Offer

Common Questions

Behavioral/STAR

Case Study

Technical Knowledge

Past Experience

Culture Fit