Reporting and Mapping Analyst

Date: Dec 5, 2018

Location: Rahway, NJ, US

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Requisition ID: CLI008194

Merck & Co., Inc. Kenilworth, N.J., U.S.A. known as Merck in the United States and Canada, is a global health care leader with a diversified portfolio of prescription medicines, vaccines and animal health products. The difference between potential and achievement lies in the spark that fuels innovation and inventiveness; this is the space where Merck has codified its legacy for over a century. Merck’s success is backed by ethical integrity, forward momentum, and an inspiring mission to achieve new milestones in global healthcare.


Merck is on a quest for cures and is committed to being the world’s premier, most research-intensive biopharmaceutical company. Today, we’re doubling down on this goal. Merck Research Laboratories is a true scientific research facility of tomorrow, and will take Merck’s leading discovery capabilities and world-class small molecule and biologics R&D expertise to create breakthrough science that radically changes the way we approach serious diseases. 

 

The CRF Submit Business Analyst is responsible for functions supportive of archiving data for the sites.  This includes: receiving notification/request for archive of data for an EDC trial that has locked, tracking study archive status, creating documentation to include with the patient data, running the CRF Submit tool to acquire patient eCRF PDFs, burning CDs specific to sites, forwarding CDs to appropriate team for release to sites, request removal of trial from production servers and archiving final study dumps.

Qualifications

Education Minimum Requirement:

  At least B.A. or B.S. degree.

 

Required Experience and Skills**:

1. Basic understanding of the Data Management process from study start-up through close-out)

2. Basic awareness of ICH-GCP guidelines as they related to study documentation

3. Computer skills (Excel, Access, InForm CRF Submit, InForm)

4. Sense of urgency and customer focus

5. Good communication skills (oral and written) with the ability to communicate with both the technical and business areas.

6. Exceptional organizational and problem-solving skills.

7. Ability to work independently with minimal supervisor

8. Ability to work cross functionally and as part of a team.

9. Ability to work under pressure and change environment with flexibility.

 

Your role at Merck is integral to helping the world meet new breakthroughs that affect generations to come, and we’re counting on your skills and inventiveness to help make meaningful contributions to global medical advancement. At Merck, we’re inventing for life. 

 

If you need assistance and/or a reasonable accommodation due to a disability during the application or the recruiting process, please send a request to staffingaadar@merck.com.

  

Search Firm Representatives Please Read Carefully: 

Merck & Co., Inc. is not accepting unsolicited assistance from search firms for this employment opportunity.  Please, no phone calls or emails.  All resumes submitted by search firms to any employee at Merck via email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck.  No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

 

For more information about personal rights under Equal Employment Opportunity, visit:

 

            EEOC Poster

            EEOC GINA Supplement 

          OFCCP EEO Supplement

 
Merck is an equal opportunity employer, Minority/Female/Disability/Veteran – proudly embracing diversity in all of it’s manifestations.


Job: Clinical Data Management
Other Locations:
Employee Status: Regular
Travel: No
Number of Openings: 1
Shift (if applicable): N/A
Hazardous Materials:
Company Trade Name: Merck


Nearest Major Market: New York City
Nearest Secondary Market: Newark

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