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Job Details

COVANCE UK - we are currently recruiting Drug Safety Associate in Maidenhead to process full service SAEs (including narrative writing)

Company: Covance
Location: Maidenhead
Reference: 41628BR
Closing Date: 14 Dec 16
Type: Permanent
Salary (£): Competitive
Benefits:

Job Summary:

COVANCE UK - we are currently recruiting Drug Safety Associate in Maidenhead to process full service SAEs (including narrative writing). More details http://careers.covance.com/job-postings/41628BR/drug-safety-associate

Requirements:

COVANCE is a leading global drug development services company and we provide support to the Pharmaceutical and Biotechnology industries. 

You can make a difference by helping to deliver life-saving and life-enhancing medicines to people around the world. Our commitment to this mission has resulted in Covance’s impressive history of company stability and growth. We’ve achieved these results by fostering a work environment that encourages, develops and leverages our team’s capabilities. 
This is your chance to become part of a team that helps to bring miracle of medicine to market sooner. 

We are currently recruiting Drug Safety Associate in Maidenhead to to process full service SAEs (including narrative writing). 

About the Job: 

• Assist with the overall Clinical Safety and/or PV&DSS operations associated with products including the entire adverse events process: which may include safety data collected from clinical trials and/or post marketing setting (i.e., unsolicited reports). 

• Manage and process expeditable adverse events to the required standard and submit them to the client and the regulatory agencies (if required) within the agreed/stated timelines. Responsible for providing this service to clients either as a support function to the client project groups or as stand-alone business. 

• Responsible to provide all clients, both internal and external, with the appropriate quality of service in a safe and cost-effective manner. 

About You: 

• Safety experience including actual experience processing AE/SAE reports, generating narratives, queries, working within safety databases, and experience with regulatory 
• Typically have a life science degree or equivalent 
• Pay attention to detail 
• High degree of accuracy with attention to detail. 
• Functions as a team player. 
• Good Communication. 
• Knowledge of medical and drug terminology desirable. 
• Familiarity of Good Clinical Practice (GCP) related to clinical safety documentation. 
• Familiarity with ICH Guidelines 
• Familiarity of worldwide regulatory requirements and reporting of adverse event for both marketed and investigational products. 
• Familiarity of worldwide regulatory requirements and reporting of adverse event for both marketed and investigational products. 
• Good written and verbal communication skills. 
• Ability to work independently with moderate supervision. 
• Good keyboard skills, preferably with knowledge of MS office and Windows would be beneficial. 

THERE IS NO BETTER TIME TO JOIN US!

Education/Qualifications

Experience

EEO Employer

Covance is committed to diversity in the workplace and is an equal opportunity employer. Your confidentiality and privacy are important to us.

Apply for this job: COVANCE UK - we are currently recruiting Drug Safety Associate in Maidenhead to process full service SAEs (including narrative writing)

Contact Information:

Address:  Covance- Brussels


Belgium
Tel: 
Fax: 
Website:  Visit Our Web Site

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