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Clinical Trial Operations Manager I

Artechinformationsystemllc
BridgewaterLead / ManagerContract
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The job in short

Clinical trial operations management.

AuditRecruitmentPharmacyClinicalCompliance

Details

Found
6 d ago · posted 2016-01-26
Location as listed
Bridgewater, NJ, US
Role
Lab / Clinical Research
Source
The company’s own careers site

Full description

Company Description Artech is the 10th Largest IT Staffing Company in the US, according to Staffing Industry Analysts' 2012 annual report. Artech provides technical expertise to fill gaps in clients' immediate skill-sets availability, deliver emerging technology skill-sets, refresh existing skill base, allow for flexibility in project planning and execution phases, and provide budgeting/financial flexibility by offering contingent labor as a variable cost. Job Description The Trial Supplies Operations Manager is responsible for the implementation of appropriate Clinical Supplies strategies and processes in order to achieve clinical study objectives in assigned programs. Responsibilities Include: • Receives the Extended Synopsis/protocol and will provide feedback /comments to Project leaders and Clinical teams • Obtain detail information about Clinical trials assigned including IP design, countries, blinded or open label trials, distribution strategy and other details. • Work in collaboration with other functional team to identify forecasting strategy, IP/Ancillaries/comparators and other requirements for the assigned trials. • Monitoring patient recruitment and adjust the resupply strategy as needed. • Work in collaboration with internal and external stakeholders to plan the labeling requirements, packaging plan and domestic and international distribution. • Initiates label request for clinical supplies meeting regulatory requirements for each market. • Monitor the distribution plan including the IVR activities, making sure that IP are delivered in good condition for patients al all the time. • Responsible for the Pre-Audit preparation for assigned trials, making sure that all documentation is correct and available for internal and external auditors. • Interaction with local country representatives (IPM) and depots to coordinate over-labeling and/or rework operations. • Constant interaction with quality (SQO), making sure that all activities related with assigned studies are within compliance. Skills • Strong verbal and written communication skills are required. • Demonstrated ability to work effectively in a global matrix team environment • Able to manage multiple projects and interact with different functional groups • Work under pressure and tight timeliness Qualifications Education • Bachelors Degree (Science) required • A degree in Pharmacy (Pharm.D) or Master degree prefered. • 3 - 5 years of hospital pharmacy or equivalent pharm Additional Information Thanks & Regards, Akriti Gupta Associate Recruiter Artech Information Systems LLC 360 Mt. Kemble Avenue, Suite 2000 | Morristown, NJ 07960 Office: 973.967.3409 | Fax: 973.998.2599 Connect with us on - LinkedIn | Facebook | Twitter

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