Helena Hallberg Email & Phone Number | MSc Biomedicine with experience of clinical trials and currently working within Regulatory Affairs. Eight years of professional experience in production and R&D in the pharmaceutical industry. Experience in analytical quality control and quality assurance in accordance with current GMP. Accountability for substance, formulation and formulation analysis in pre-clinical toxicity studies according to GLP. Principal Investigator for formulation analysis in studies performed at CROs. Collaborated with a large global network of contacts both internally and externally to support pre-clinical safety assessment and have experience interacting with people from different professional backgrounds. A positive person with great commitment and good organizing skills who enjoy working in a wide network and like working in teams.

Helena Hallberg

MSc Biomedicine with experience of clinical trials and currently working within Regulatory Affairs....
Greater Stockholm Metropolitan Area, Greater Stockholm Metropolitan Area, Sweden

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Helena Hallberg’s Email helena.hallberg@astrazeneca.com

Helena Hallberg’s Phone Numbers +46 46 33 6****

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Helena Hallberg’s Location Greater Stockholm Metropolitan Area, Greater Stockholm Metropolitan Area, Sweden

Helena Hallberg’s Current Industry Astrazeneca

Helena Hallberg’s Prior Industry Amgen | Quintiles

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Work Experience

Astrazeneca

Regulatory CMC Manager

2018-01-01 00:00:00 - Present

Amgen

Regulatory Affairs Associate/Manager (DOCS consultant)

2016-01-01 00:00:00 - 2018-01-01 00:00:00

Quintiles

Clinical Trial Associate (Amgen)

2015-03-01 00:00:00 - 2015-12-01 00:00:00

Skills

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Languages

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FAQ About Helena Hallberg

Helena Hallberg is located at
Greater Stockholm Metropolitan Area, Greater Stockholm Metropolitan Area, Sweden

Helena Hallberg is a MSc Biomedicine with experience of clinical trials and currently working within Regulatory Affairs. Eight years of professional experience in production and R&D in the pharmaceutical industry. Experience in analytical quality control and quality assurance in accordance with current GMP. Accountability for substance, formulation and formulation analysis in pre-clinical toxicity studies according to GLP. Principal Investigator for formulation analysis in studies performed at CROs. Collaborated with a large global network of contacts both internally and externally to support pre-clinical safety assessment and have experience interacting with people from different professional backgrounds. A positive person with great commitment and good organizing skills who enjoy working in a wide network and like working in teams.