Global Clinical Trial Project Mgr vacancy at Aerotek Scientific in Exton

Aerotek Scientific is hiring Global Clinical Trial Project Mgr on Fri, 06 Jul 2012 22:42:36 GMT. Our biotech client is rapidly growing and is need for a Global Clinical Trial Project Manager based in Exton, PA. (This is a direct placement effort with our client.) They are looking for someone with a Neurology background. SUMMARY Global Clinical Trial Project Manager leads and manages both national and global clinical projects and their associated clinical teams including schedule and budget...

Global Clinical Trial Project Mgr

Location: Exton Pennsylvania

Description: Aerotek Scientific is hiring Global Clinical Trial Project Mgr right now, this vacancy will be placed in Pennsylvania. Further informations about this vacancy opportunity kindly see the descriptions. Our biotech client is rapidly growing and is need for a Global Clinical Trial Project Manager based in Exton, PA. (This is a direct placement effort with our client.) They are looking for someone with a Neurology background.

SUMMARY

Global Clinical Trial Project Manager leads and manages both national and global clinical projects and their associated clinical teams including schedule and budget responsibilities for clinical trial execution. The incumbent also ensures clinical trials are conducted in accordance with Company’s clinical procedures, ICH GCP Guidelines and national regulations. The incumbent also provides guidance and direction to other clinical staff to ensure the successful implementation and execution of other clinical trials.

ESSENTIAL DUTIES AND RESPONSIBILITIES include the following. Other duties may be assigned.

1. Manages overall operation of entire clinical study(ies) including but not limited to project planning, budget, resource management and CRO management; 2. Participates in developing, modifying and executing company policies that affect immediate operations and may also have company-wide impact; 3. Develops study related documents and participates in setting overall direction for clinical sites to establish protocol development; 4. Reviews study documents such as protocols, Investigator brochures, DMPs, CRFs, SAPs, FCSR and regulatory filings; 5. Recommends and based on approval, implements innovative process ideas to impact clinical trial management; 6. Acts as cross-functional liaison to ensure study plan(s) aligns with business development strategies; 7. Oversees and maintains relationships with CROs; 8. Evaluates and analyzes tools and processes to support outsourcing efforts. 9. Travel with 50% both domestic and international

SUPERVISORY RESPONSIBILITIES

Provides leadership and guidance to other clinical staff.

QUALIFICATIONS:
EDUCATION

• BA/BS in nursing or other related discipline.
• Work experience may be considered in lieu of educational requirements.

EXPERIENCE 1. Minimum of 7 years of clinical experience in a CRO, global pharmaceutical, biotechnology or medical device environment.

• Experience with biologics and/or vaccines in the company’s therapeutic areas a plus.
• Knowledge of multiple therapeutic areas a plus.

2. Minimum of 5 years of in clinical trial management. 3. Minimum of 3 years previous people management experience.

Full Benefits and paid time off are provided in this position. Interested candidates should contact Laura Walton at 201-793-1006.
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If you were eligible to this vacancy, please email us your resume, with salary requirements and a resume to Aerotek Scientific.

If you interested on this vacancy just click on the Apply button, you will be redirected to the official website

This vacancy starts available on: Fri, 06 Jul 2012 22:42:36 GMT

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