Clinical Trial Manager job Parsippany New Jersey
Clinical Trial Manager job Parsippany New Jersey
My Spider Scam Awareness Contacting Us F. A. Q.
Job Seekers
Search Jobs
Browse Jobs
Post a Resume
Job Alerts
Search Resumes
Browse Resumes
Post a Job

Clinical Trial Manager Job

Employer Name: Ferring Pharmaceuticals SpiderID: 8745080
Location: Parsippany, New Jersey Date Posted: 6/17/2019
Wage: Category: Management
Job Code: R0009978

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 over 5,700 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) and orthopedics.  Ferring’s US operations employ approximately 800 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: See responsibilities and requirements below.

* Leadership of Clinical Team (timelines, quality financial oversight, routine meetings)
* Responsible for all operational aspects of clinical trial oversight including the delivery of every study on time within budget and in compliance with GCP’s, SOPs and standards
* Study Plan development (Safety Monitoring Plan, DSMB Plan, Trial Risk Management Plan, SOP usage, protocol deviation plan) Vendor specifications and oversight
* Site selection
* Oversight of DSMB and Steering Committee Activities
* Audit / inspection Communication and Coordination of CAPA activities
* Responsible for the coordination of internal/external resources and third parties/vendors for the flawless execution of the study.
* This role is also responsible for the preparation of study related materials, relationship management between clinical sites and vendors, and identification of project risks and contingency planning. You must be comfortable working independently, managing interactions with and between clinical monitors, biostatistics, medical writing, safety and other key stakeholders.
* Ensure proper documentation availability
* Ensure proper collection and validation of data and documentation in a timely manner
* Organize and lead study specific meetings
* Collect, synthesize and report study information
* Collaborate with the Clinical Supplies to validate Investigational Medicine Products (IMP) needs, specifications, packaging, shipment (including resupply) and reconciliation process
* Participate in selection and management of vendors, development/follow-up of the associated budget
* Preparation and oversight of study audits/inspections both internal and external
* Provide oversight and preparation for FDA pre-approval inspections (PAI)

Job Requirements:
* BA or BS degree in Life Science required
* 7+ years of clinical trial experience
* At least 5 years clinical trial management experience

* Thorough knowledge of GCP/FDA/ICH regulations required
* Thorough understanding of clinical research principles and process
* Experience with study start-up, timeline planning and management and financial management of clinical trials including vendor oversight required
* 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
* Critical thinking and problem- solving mindset

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:

Send ad to a friend
Report a Problem


© 2019 Job Spider
Privacy Policy | CC Marketing Sites | Site Map | Links