Lead Study Manager: Full-time/ Low Travel, Global Studies (bcs659BHmo)

Lead Study Manager: Global Studies, Top-Ranked Company- Large Pharma, Montclair, NJ,

 

Our client is an industry leading global pharmaceutical company with an excellent reputation as an employer who takes care of its people. They have one of the top two pipelines and have just recently been ranked by a major publication as the Top Pharmaceutical Company in the industry.  They are currently in search for an established Study Manager to run multiple studies across multiple therapeutic areas.  You will enjoy a very competitive compensation plan, as well as exceptional benefits.  Note: All inquiries and submissions are held in strict confidence (see our privacy policy below). 

 

Position Title: Lead Study Manager

 

Company Description: Just ranked as the Pharmaceutical Company of the Year.  Multiple blockbuster products across several therapeutic areas, top rated pipeline, and always ranked as a top employer to work for.

 

Location:  Montclair, New Jersey area

Attractive features about this position and company: This Company is continuing to grow an already robust Clinical Research and Development department with multiple leading products as well as a stout pipeline.Opportunity.  You will serve as the “quarterback” who will be the crucial team member in regards to managing multiple studies. Growth.  There is a clear growth path within the company and we have seen many people advance their career from within.Great location for those not only in NJ (North/East/West/Central), but also from NYC, Southern CT, or NY counties north of NYC.  Easily accessible from Route 80, 46, 287, and 3 as well as the NJ Turnpike and Garden State Parkway.Firm has a strong reputation for taking care of its people.  They are annually ranked as a top employer to work for (Fortune, NJ Biz, and Science) and are also ranked by Mothers Magazine as a leading employer for working mothers.

Responsibilities, Challenges, Expectations and Deliverables for this position:Provides direction and leadership to one or more clinical operations teams.In a nutshell, you will be responsible for managing all aspects of international clinical trials from study start-up through close-out. This includes responsibilities across operations, development, and project management. Overseeing the overall strategy of the international clinical trials. Manage both internal regional/traveling monitors as well as CRO staff. Manage tracking systems for drug supply and use, enrollment of subjects, regulatory document flow, study timelines, financial information, Serious Adverse Events, performance metrics, data flow, etc. Cross functional management/participation (e.g., data management, clinical science, statistics, etc) for the duration of trials. Budget, timeline, and resource management across your assigned trials.

Compensation/Benefits: Base compensation can range from $90k-$120k based on your level of experience and will also include a competitive bonus and top-tier benefits such as 100% tuition reimbursement, a generous 401(k) plan, and exceptional on-site facilities/perks including Child Care, On-site Gym, etc.

 

Experiences, Skills, Accomplishments and Qualities Desired:Masters degree preferred.  BS/BA degree required.5-7 years of experience gained with a CRO or Pharmaceutical Company working on Phase I - IV clinical studies.  Our client will not consider candidates without Pharma or CRO experience.Multiple therapeutic areas are accepted.Experience managing CROs/monitors.Budgeting, timeline/resource management, and contract negotiation experience.Protocol and CRF review.  You do not need to have written protocols.

Other Opportunities:

Our firm specializes in Pharmaceutical recruiting for firms located in NJ, NYC, and the surrounding areas. In addition to this opportunity, we are helping many of our other clients, located in Central NJ, Northern NJ, and NYC, on other CRA, SR. CRA and Clinical Project Management full time and consulting positions. For description of those opportunities, please visit our site www.cornerstonesg.com.

 

Cornerstone’s Privacy Policy

Cornerstone Search Group considers all inquiries, resume submissions, and any other personal information submitted to us as confidential information.  This information will not to be shared with any parties outside of Cornerstone Search Group without your prior permission.

 

Contact:

Brian Skurka

Client Consultant, Pharmaceutical Recruiting Practice

 

Cornerstone Search Group, LLC

9 Sylvan Way

Parsippany, NJ 07054

P 973-656-0220

bskurka@cornerstonesg.com (initial contact via email is preferred)

 

Web/URL: www.cornerstonesg.com

 

About Cornerstone Search Group, LLC

Cornerstone Search Group is a specialty pharmaceutical recruiting firm located in the heart of New Jersey's Pharmaceutical Corridor. We help our clients hire experienced pharmaceutical professionals from the Staff through Management (VP/Director) levels for Full-Time and Contract positions. We provide our professional recruiting services on a Contingency, Retingency, or Retained basis to best suit the hiring needs of our clients.

 

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