Pharmiweb ChannelsAll | PharmaCo | Clinical Research | R&D/BioTech | Sales/Mktg | Healthcare | Recruitment | Pharmacy | Medical Comms

Pharmiweb.com RSS Feed Pharmiweb.com RSS Feeds

Pharmiweb.com RSS Feed PharmiWeb Candidate Blog

Pharmiweb.com RSS Feed PharmiWeb Client Blog

Job Details

Senior Clinical Research Associate - Specialist Global CRO - Spain

Company: Barrington James Clinical
Location:
Reference: ACCRA100817
Closing Date: 10 Sep 17
Type: Permanent
Salary (£): Competitive
Benefits:

Job Summary:

Alex Coppen

Requirements:

Role: Senior Clinical Research Associate (Will consider CRA II)

Location: Spain - Barcelona/Spain

Company: Small, global CRO (rare/complex disease)

Salary: Competitive

Do you want to be involved in more than monitoring? Are you working on a huge amount of studies at once, traveling too much and looking to focus on the quality of your work?

To be considered for this role:

Degree in life sciences.
4 or more years monitoring in clinical research experience: preferably in a CRO
IMP trial experience
Oncology experience is highly recommended - Other TA experience should ideally encompass complex indications and/or rare disease and/or trials in ICU settings
Experience in EC and regulatory submissions would be a bonus
Ability to work home based


I have recently met with the Head of Clinical Operations for a small-medium sized, specialist, global CRO who are looking to expand across Europe. The company specialises in working with small-medium Biotech’s on rare, complex studies that have huge potential to change people’s lives, often indications that have a high unmet medical need.

 

The company offers a both a professional and family environment where everyone knows each other and there are short lines of communication within the company. People are not numbers on a spreadsheet. 

 

You will be able to develop a wide range of skills as you will not only be monitoring, but will be involved in SSU activities such as EC submissions and contract negotiations. They are conscious that their CRAs are involved in more than monitoring, so they do not ask them to monitor 12 to 15 times per month. The more Senior CRAs also get the chance to evolve as Lead CRAs on some studies in order to develop new management skills.

 

The role will include:

Administration and full investigator site responsibility for clinical studies according to Standard Operating Procedures (SOPs), ICH-GCP and local regulations
Acts as mentor for less experienced CRAs
Senior CRA - May act as lead CRA assisting a Project Manager (PM) and may act as lead CRA or as a PM of national studies
Ensures clinical trials are monitored such that subjects' rights, safety and wellbeing are protected and that the clinical trial data are reliable
Assists the PMs in the preparation and review of protocols and informed consent forms
Negotiates investigator budgets and assists with the execution of site contracts with support from the legal department
EC and regulatory submissions

 

If you are looking for a company that invests in its people, enables you to work within rare indications and offers opportunities to grow and challenge yourself, this could be your next move. 

For more information on the opportunity, send me an email at acoppen@barringtonjames.com or even better, call 01293776644

Alex Coppen

Apply for this job: Senior Clinical Research Associate - Specialist Global CRO - Spain

Contact Information:

Address:  Head Office
Victoria House
Consort Way
Horley
Surrey
RH6 7AF
England
Tel:  01293 776644
Fax:  01293 822333

Advertising
Share | | |
Site Map | Privacy & Security | Cookies | Terms and Conditions

PharmiWeb.com is Europe's leading industry-sponsored portal for the Pharmaceutical sector, providing the latest jobs, news, features and events listings.
The information provided on PharmiWeb.com is designed to support, not replace, the relationship that exists between a patient/site visitor and his/her physician.