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Senior Clinical Quality Assurance Associate - GCP experienced
Encorium Group, Inc.
Wayne, PA
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Encorium is a full-service Contract Research Organization (CRO)
providing comprehensive solutions for pharmaceutical, biotechnology, and
medical device companies with 23 years experience representing over 30
countries. Encorium has over 250 professionals working internationally
with our Global Headquarters located in Wayne, Pennsylvania and our
European Headquarters in Finland. Please visit us at
www.encorium.com
We value high quality, flexibility, honesty and trust. Our team in
Wayne, Pennsylvania is growing and we are looking for a
Senior Clinical Quality Assurance Associate with GCP experience
With minimal management oversight the qualified candidate will be
responsible for:
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Professional communication with Encorium and Sponsor study team members
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Ensuring
set-up and maintenance of the QA Central File (department and
project-specific) |
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Participating/Conducting all applicable QA activities (i.e. Audit Plan,
ICF reviews, site audits, database audits, CSR audits to ensure
compliance to applicable regulations., Encorium Procedures and ICH/GCPs.
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Assisting
in the identification of areas and/or individuals that require
additional training and ensure appropriate training sessions are
conducted (i.e. audit observations). |
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Assisting
in providing Good Clinical Practice (GCP) training to Encorium, and/or
Sponsor, investigative site, personnel through presentations and
meetings, as applicable. |
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Assisting
in the development, implementation and training of QA Procedures and
other Encorium Procedures. |
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Responsible for providing training, mentoring and support to QA and/or
Encorium personnel, as appropriate. |
The qualified candidate MUST have the
following minimum requirements:
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Bachelor’s
degree in a life science/related area (e.g. biology; chemistry) with 4 or
more years of clinical research experience and 3 or more years recent
auditing (preferred) or monitoring experience. |
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Demonstrated expertise in Quality Assurance procedures, through
knowledge of the drug development process, FDA regulations and guidance
documents, ICH guidelines, strong oral and written skills, effective
problem-solving skills and ability to orchestrate multiple activities at
one time. International experience a plus. |
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Experience
with the development, implementation and management of corporate and
departmental policies and procedures and be able to ensure that
employees comply with them. |
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Strong
interpersonal skills and be able to build constructive relationships
both internally and with sponsor personnel. |
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Be able to
consistently meet deadlines and complete tasks according to established
levels of quality. |
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Approximately 30% travel. |
To
apply: email resumes with salary requirements to
hr@encorium.com
E/O/E
Search Firm Representatives, Please Read Carefully.
Encorium is not seeking assistance or accepting unsolicited resumes from
search firms for this employment opportunity. Regardless of past
practice, all resumes submitted by search firms to any employee at
Encorium via-email, the Internet or directly to hiring managers at
Encorium in any form without a valid written search agreement in place
for that position will be deemed the sole property of Encorium, and no
fee will be paid in the event the candidate is hired by Encorium as a
result of the referral or through other means. |