Senior/Clinical Research Associate II - South West England - FSP
at Parexel
Remote, Scotland, United Kingdom -
Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
---|---|---|---|---|---|---|---|
Immediate | 21 Jan, 2025 | Not Specified | 21 Oct, 2024 | N/A | Clinical Trials,Interpersonal Skills,Terminology,Time Management,Clinical Research,Addition | No | No |
Required Visa Status:
Citizen | GC |
US Citizen | Student Visa |
H1B | CPT |
OPT | H4 Spouse of H1B |
GC Green Card |
Employment Type:
Full Time | Part Time |
Permanent | Independent - 1099 |
Contract – W2 | C2H Independent |
C2H W2 | Contract – Corp 2 Corp |
Contract to Hire – Corp 2 Corp |
Description:
Parexel is currently seeking Senior & Clinical Research Associate IIs in South West England.
These will be home-based positions and fully dedicated to a single sponsor.
Working as a Senior or Clinical Research Associate II at Parexel offers tremendous long-term job security and prospects. We undertake vital clinical studies for sponsors including the leading global biotechs and Pharma top 50. And we have an incredible pipeline of work.
Whether you see your future path as a CRA, or in fields such as clinical operations, project management, line management, or other positions, we have a world of opportunity waiting for you.
Our CRAs work from their home office base, supporting studies within their country or region. ‘Manageable sites, manageable protocols’ is our mantra. Expect exciting professional challenges in inspiring studies, but with time for your outside life.
Responsibilities:
SOME SPECIFICS ABOUT THIS ADVERTISED ROLE
- Dedicated to one client.
- Responsible for all site management and monitoring activities across assigned oncology studies
- Work with industry leaders and subject matter experts.
- Opportunity to mentor junior CRAs.
- Work with world-class technology.
- A pivotal role in the drug development process.
HERE ARE A FEW REQUIREMENTS SPECIFIC TO THIS ADVERTISED ROLE.
- Substantial Site Management experience, with an understanding of the clinical
- trial methodology and terminology.
- Experience in, or willingness to monitor oncology clinical trials.
- Experience in independent monitoring, all types of visits.
- Effective time management, organizational and interpersonal skills & problem-solving skills, with the ability to multi-task and prioritize.
- Good understanding and working knowledge of clinical research, phases of clinical trials, current GCP/ICH & country clinical research law & guidelines.
We care about our people and your passion, as they are the key to our success, and provide an open and friendly work environment where we empower people and provide them with opportunities to develop their long-term careers. In addition, you will have the opportunity to develop within your role and tackle further responsibilities or develop your skill set within other related departments of Parexel.
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REQUIREMENT SUMMARY
Min:N/AMax:5.0 year(s)
Pharmaceuticals
Pharma / Biotech / Healthcare / Medical / R&D
Clinical Pharmacy
Graduate
Proficient
1
Remote, United Kingdom