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Job Details

Regulatory Submissions/ Study Start Up

Company: Planet Pharma Staffing Limited
Location: Rotterdam, Netherlands
Reference: RHSSU
Closing Date: 11 Aug 18
Type: Permanent
Salary (£): Competitive
Benefits: On application

Job Summary:

You will play a key role in the management process for study start up and clinical trials by managing start-up of projects while being provided with training to ensure career progression. Please apply if you are interested in finding out more!

Requirements:

Job Title


Regulatory Submissions/ Study Start Up

Location

Office-based in Rotterdam, Netherlands 

Company Statement

Our client is a full service global CRO that has been in the market for over 25 years and soon becoming one of the main providers for many top 10 pharmaceutical, bio-tech and start-up companies.

They have been awarded several times as a top-quality provider organization and rewarded of their therapeutic excellence which is reflected in their commitment to continue growing and investing in their employees. They have excellent training programs in place tailored to your needs that will ensure that everyone working there will become an expert in their field and be able to offer the highest quality to clients. Furthermore, the fact that they are a mid-sized company means that you will have the chance to really take ownership of your own work as well as achieve quick career progression from day one.

 

Summary

You will play a key role in the management process for study start up and clinical trials by managing start-up of projects while being provided with training to ensure career progression.

Role/ Description

Responsibilities:

  1. Responsible for managing all aspects related with global start-up activities
  2. Prepare and review clinical trial applications
  3. Ensure that submissions are compliant with regulations and deadlines are met
  4. Advise sponsors on compliance requirements and regulations
  5. Requirements:
  6. Bachelor’s degree required
  7. At least 1 years of experience in a similar position
  8. Experience with the preparation, revision and submission of regulatory documents
  9. Excellent oral and communication skill

About Planet Pharma

Planet Pharma is an American parented Employment Business/Agency that provides global staffing services with its head-quarters in Chicago and our EMEA regional office located in Central London. We have invested significantly in creating a robust international platform that enables us to work compliantly in 30+ countries with a current network of 2500+ active contractors globally as well as a very strong permanent / direct hire recruitment offering.

Our specialist knowledge and close relationships with our clients and the wider industry really makes us unique in our field. Just recently we were recognised by FORBES as the 17th best professional staffing firm, and have won multiple awards from industry accredited bodies for our commitment to excellence and service delivery. We have extensive functional expertise including: Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs / Writing.

We are an equal opportunities Recruitment Business and Agency. We welcome applications from all suitably qualified candidates regardless of their race, sex, disability, religion/belief, sexual orientation or age.

www.planet-pharma.com

 

To apply 


If you would like to discuss this vacancy further or to discuss your career options in confidence, please telephone on +44 (0)20 3868 1012 or e-mail Rowena on rhorn@planet-pharma.co.uk

If this role isn’t suitable for you, please let us know if you can refer anyone – any recommendations are much appreciated! Planet Pharma offers a competitive referral scheme so you will be rewarded for your help!

 

Keywords

Study start up, submissions, regulatory, bid defenses

Apply for this job: Regulatory Submissions/ Study Start Up

Contact Information:

Address:  Head Office
10 Greycoat Place, London,
SW1P 1SB
England
Tel:  +44 203 868 1000
Website:  Visit Our Web Site

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