Senior Clinical Research Associate (Northwest) job Parsippany New Jersey
Senior Clinical Research Associate (Northwest) job Parsippany New Jersey
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Senior Clinical Research Associate (Northwest) Job

Employer Name: Ferring Pharmaceuticals SpiderID: 8745119
Location: Parsippany, New Jersey Date Posted: 6/17/2019
Wage: Category: Science/Research
Job Code: R009822

Job Description:
Ferring Pharmaceuticals is a research-driven, specialty biopharmaceutical group committed to helping people around the world build families and live better lives. Ferring is a leader in reproductive medicine and women’s health, and in specialty areas within gastroenterology and urology. Ferring employs approximately 6,500 people worldwide, has its own operating subsidiaries in nearly 60 countries and markets its products in 110 countries. Learn more at and @Ferring, or connect with us on Facebook, Instagram and LinkedIn.

Ferring Pharmaceuticals is a globally recognized, research-driven, biopharmaceutical company with more than 65 years of history. Headquartered in Switzerland, Ferring is privately owned with approximately 6,500 employees in nearly 60 countries. In the United States, Ferring identifies, develops and markets innovative products in the fields of reproductive health (infertility), urology, gastroenterology, endocrinology, women’s health (obstetrics/gynecology), orthopedics and Oncology.  Ferring’s US operations employ approximately 900 people.
People Come First at Ferring. The Ferring Philosophy places people at the heart of what we do. This guides our relations with patients, physicians, employees, and other stakeholders. We invite you to share our passion for people and the power of science.

Summary: Responsibilities and requirements for Clinical Trial Associate are below.

* Study Plan creation (Oversight plan, Monitoring plan, patient recruitment)
* Assist with Vendor selection and payments
* Review of site feasibility documents
* Design of data collection tools (eCRF, ePRO, IRT)
* Assist in development of protocol and create ICF and other patient materials
* Investigator Meetings and Training Support
* Study Team Training
* Monitoring Trip Report Review and Approval
* Data cleaning
* Protocol deviation tracking
* Site Issue Management
* Trial Master File Quality Review and Follow Up

Job Requirements:
* BA or BS degree in Life Science or equivalent preferred.
* Minimum 3-5 years clinical trial experience.
* Prior data review/remote monitoring experience.
* Thorough knowledge of GCP/FDA/ICH regulations required.
* Thorough understanding of clinical research principles and process
* Proficient in MS Excel, Word and PowerPoint.
* Experience with data collection processes, data review and comfort with using technology including analytics tools.
* Excellent organizational and time-management skills.
* Strong interpersonal skills.
* Effective verbal and written communication skills including presentation skills.
* Team player and able to work independently.
* Ability to work well under pressure and with tight schedules.
* Ability to identify critical issues and escalation to leadership when appropriate.

We are proud to be an Affirmative Action/EEO Employer.  EOE Minorities/Females/Protected Veterans/Disabled

We maintain a drug-free workplace and perform pre-employment substance abuse testing.

Location: Parsippany

To view or apply online:

Job Criteria:
Start Date:
Position Type: Full-Time Permanent
Years of Experience Required:
Education Required:
Overnight Travel:
Vacation Time:

Contact Information:
Contact Name: Randie Zimmerman Company Type: Employer
City: Parsippany
State: New Jersey
Web Site:

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