Freelance QA/QC consultants based in Israel

Due to the geographic spread of study sites, we are looking for experienced freelance industry professionals to join our Quality Assurance (QA) team. This contract will support and audit global trials based in Israel, in a variety of therapeutic areas, maintaining organizational and regulatory standards. This is a vital role in the Quality Assurance of the study.

Responsibilities, all or any of the following, contract dependent : 

1.    Act as a Quality Program Lead on clinical trials by supporting national and international regulatory standards and guidance for pharmaceuticals, biologics and medical devices.

2.    Develop audit management plans and audit strategy with clients for ongoing clinical trials.

3.    Coordinate and conduct internal system audits and external investigative site/vendor audits in accordance with Good Clinical Practice (GCP) guidelines;

4.    Participate in the development of departmental standard operating procedures, work instructions, forms, and templates;

5.    Develop training materials and applicable interactive tests and proficiency training including company-wide regulatory training (ICH/GCP);

Qualifications : 

1.    Bachelor’s degree in life sciences or related field; 

2.    5+ years of experience in a QA department in the biopharmaceutical industry; 

3.    Experience conducting audits of vendors and investigative sites; 

4.    Experience hosting regulatory authorities and interacting with sponsor/client representatives; 

5.    Independent thinking and planning ability; 

6.    Knowledge and application of Good Clinical Practice (GCP) is required; 

7.    Medical Device and or Phase 1 experience is a plus; 

8.    Ability to travel up to 30%-40% of time; 

9.    Excellent written and verbal communication skills; 

10.  Exceptional teamwork skills; and 

11.  Ability to work independently.

If you are interested please email [email protected] with a copy of your CV.

Pharmalancers, is a new and novel way to match experienced freelance consultants, with prospective opportunities with Pharmaceutical, Biotech companies and CROs. We currently represent over 160 consultants; who are experts  in RA (incl CMC), PV, medical writing, QA/QC, biostats, DM and project management. Our consultants are based across Europe, and throughout North America and South East Asia, and we are currently expanding into Latin America. The platform is free to join, our fees are 15% of the freelancer consultants hourly/ daily/ project rate. www.pharmalancers.com