Clinical Research Manager, Work from home (1 to 2 days):

Exciting Biopharma, Southern NY

Our client is a respected biopharmaceutical company with multiple big pharma partnerships. They offer an academic atmosphere within the group and you will work alongside two very experienced and personable Directors. In this role you will serve as a key member of the Clinical Development team managing CROs, protocol development, data management, etc. Compensation is competitive and will also include a double-digit bonus, stock options, strong benefits, etc. The team is flexible and is open to considering candidates that would need to work a day or two from home. Relocation assistance can also be offered.

Note: All inquiries and submissions are held in strict confidence (see our privacy policy below).

Position Title: Clinical Research Manager

Company Description: Our client is a highly respected biopharmaceutical company that has multiple partnerships with big pharma leaders. They have a strong pipeline across multiple therapeutic areas. They offer a collegial working atmosphere on a beautiful campus setting.

Location: Nyack , NY area

Attractive features about this position and company:

· Work from Home Option: There is the ability to work a day or two from home.

· Impact: As a member of a smaller company, your contribution is not only highly visible, it’s felt every single day.

· Team: You will be a very important contributor to a talented and motivated team of professionals, and not just another cog in the wheel.

· Unique Company: Exciting and innovative Biopharmaceuticals Company seeking to discover and develop novel drugs/therapies to address major medical needs.

· Unique Products: This Company has discovered and continues to discover new drugs for its medical targets.

· Stock Options: This Company offers its employees stock options so that as they continue to grow, you get to share in the excitement.

· Commutable from CT, NJ, NY State, and NYC (via public transportation).

Compensation/Benefits: Base compensation is competitive and will range depending on your experience. This will also include a bonus and top-tier benefits including: stock options, 401k match, relocation (if needed), etc.

Responsibilities: Challenges, Expectations and Deliverables for this position

· In a nutshell, you will manage clinical research projects which will include: CRO management, protocol writing/development, training clinical sites, etc.

· Interact regularly with CRO, central laboratory, and IVRS systems.

· Follow established clinical study standards and procedures to plan and conduct clinical research studies.

· Play a lead role in the development of procedures and tools for data collection.

· Apply knowledge of company policies and standard practices to resolve problems.

· Escalate non-standard problems or issues as may be required.

· Compile and maintain regular status reports of study progress.

· Play a lead role in the development of study documents including protocols, informed consent forms, and procedure manuals.

· Maintain open communication channels with study sites and members of the study team.

Experiences, Skills, Accomplishments and Qualities Desired:

· BS/BA degree in a scientific or life sciences area of study is preferred. Higher degree is desirable.

· 3-7 years of CRA experience gained with a CRO or Pharmaceutical Company working on Phase I - III clinical studies.

· Multiple therapeutic areas acceptable.

· Clinical field monitoring experience is a plus. Even though they use CROs to handle day-to-day field monitoring, they value CRAs who have such experience themselves.

· While you will not travel regularly, you do have to be flexible, as is the case with any smaller company.

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:

Thomas Fascia

Manager, Specialized Pharmaceutical Practice

tfascia@cornerstonesg.com

Cornerstone Search Group, LLC

9 Sylvan Way

Parsippany , NJ 07054

P 973-656-0220 x17

F 973-656-0228

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.

RECRUITING FROM STAFF THROUGH MANAGEMENT LEVELS IN:

- Biostatistics and SAS Programming

- Clinical Operations (CRAs, Project Managers, Management)

- Clinical Research

- Data Management / Clinical Programming

- Drug Information

- Drug Safety

- Human Resources

- Information Technology

- Marketing / Market Research

- Medical Directors

- Medical Science Liaison

- Medical Writing

- Product Management

- QA/QC

- Regulatory Affairs

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