# Clinical Research Manager

**Company**: IQVIA
**Experience**: senior
**Job type**: full-time
**Salary**: $74,600.00 - $216,000.00
**Category**: Healthcare
**Industry**: Healthcare

**Apply**: https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Durham-North-Carolina-United-States-of-America/Study-Start-Up-Manager---IQVIA-Biotech_R1545614?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply
**Canonical**: https://yubhub.co/jobs/job_69d8da1f-1b4

## Description

You will direct and manage the delivery of all required site activation, maintenance and regulatory activities for selected studies or multi-protocol programs.

Key responsibilities include:

- Overseeing site activation and maintenance for assigned projects, adhering to project timelines and strategies

- Developing, implementing and maintaining management plans according to the scope of work and project plan

- Ensuring collaboration across regulatory and site activation teams, and providing specialist regulatory and technical scientific support

- Providing guidance and oversight of multi-regional and multi-protocol programs during initial start-up and maintenance phases

- Determining regulatory strategies and expectations, and assessing regulatory landscapes

- Executing operational strategies for maintenance of clinical study approvals and authorizations

- Mentoring and coaching colleagues as required

- Delivering presentations and training to clients, colleagues and professional bodies

You will need:

- A bachelor's degree in life sciences or a related field

- 7 years' relevant experience in a scientific or clinical environment, including demonstrable experience in an international role

- Strong negotiation and communication skills, with the ability to challenge

- Excellent interpersonal skills and the ability to work as a team player

- Proven ability to work through others to deliver results on complex projects

- Thorough understanding of the regulated clinical trial environment and in-depth knowledge of the drug development process

- Demonstrated proficiency in using systems and technology to achieve work objectives

- Good regulatory and/or technical writing skills

- Strong knowledge and ability to apply Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines and applicable regulatory guidelines

Benefits may include a range of health and welfare benefits, incentive plans, bonuses, and other forms of compensation.

The potential base pay range for this role, when annualized, is $74,600.00 - $216,000.00.

## Skills

### Required
- Clinical Practice (GCP)
- International Conference on Harmonization (ICH)
- regulatory affairs
- clinical trials
- life sciences

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Source: [Apply at iqvia.wd1.myworkdayjobs.com](https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Durham-North-Carolina-United-States-of-America/Study-Start-Up-Manager---IQVIA-Biotech_R1545614?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply)