Home > Pharmaceutical & Biotech > Senior Manager, Global Trial Management (Titusville, NJ) - 0608369

Senior Manager, Global Trial Management (Titusville, NJ) - 0608369

September 2, 2010 Job Posted in Pharmaceutical & Biotech

Country: USA
Location: NJ Titusville
Total applied: 40
Job ID 0608369 Position Type Full-Time Employee Company Name Johnson & Johnson Family of Companies Location Titusville, NJ Salary Unspecified Experience 5-10 Years Experience

Description Johnson & Johnson Pharmaceutical Research & Development, LLC., a member of Johnson & Johnson's Family of Companies, is recruiting for a Senior Manager, Global Trial Management , located in Titusville, NJ. Johnson & Johnson Pharmaceutical Research & Development, L.LC develops treatments that improve the health and lifestyles of people worldwide.

Research and development areas encompass novel targets in neurological disorders, gastroenterology, oncology, infectious disease, diabetes, hematology, metabolic disorders, immunologic disorders, and reproductive medicine.

The Senior Manager, Global Trial Management is considered the study owner, will lead the Study Management Team.

Concentrates on trial management supervision, planning and coordination.

Includes trial set-up and execution, budget management, patient recruitment/retention, database closure oversight, clinical supplies management, associated with the trial(s).

Measures progress against goals to achieve clinical research targets.

Make sure commitments meet the actuals across the regions at the clinical trial level, monitors patients recruitment at the global level, and ensure timely and accurate documentation and communication of study progress and issues.

Final accountable for trial planning and deliverables/execution, strong interaction with the Central Business Operations groups, IDS including vendor management, Clinical Supplies team, and Planning unit.

Responsibilities include: Increase productivity for all clinical trials assigned, optimize relationship with R&DC, ensure required reports are generated within organization guidelines, ensure compliance with US and global regulatory agency regulations and guidelines and internal operating procedures and processes.

Participate in preparation for, and conduct of, FDA and internal QA inspections and audits.

In coordination with the clinical program leader, the GTM is responsible to ensure appropriate specific protocol training is provided to the trial coordination and site management personnel, coordinate investigator meetings.

Qualifications A minimum of a Bachelors degree is required, preferred in Life Sciences (e.

g., Biology, Chemistry, Biochemistry, Nursing, Pharmacy).

A minimum of 7 years of industry related clinical trials experience in the pharmaceutical industry as a clinical trials professional is required.

Experience managing and executing clinical trials is required.

Experience managing global trials is preferred.

Experience managing CROs is preferred.

Project management with Global Clinical Trials is preferred.

Strong operational expertise, project planning, strong organization skills, excellent decision-making and strong financial management skills are required for this position.

Effective leadership skills and proven ability to foster team productivity and cohesiveness is required.

Excellent communication skills coupled with the innate flexibility to work in a rapidly growing organization.

Computer literacy is also required.

If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today! To learn more about opportunities with the Johnson & Johnson Family of Companies, visit us at www.jnj.com/careers. Johnson & Johnson is committed to diversity and invites all interested candidates to bid on positions of interest.

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