Alpha Consulting Corp.
JOB DETAILS
JOB TYPE
Full-time
LOCATION
Madison, NJ
POSTED
13 days ago

Description

  CLINICAL TRIAL MANAGER
MADISON, NJ
 
Position Remote.
 
Project Description:
  • Responsible for supporting the Senior Clinical Trial Manager/operational study lead, and for managing various aspects of the operational execution and delivery of quality studies, including in process quality control activities (e.g., quality checks and balances to ensure inspection readiness, Enrollment, Metrics, Milestones, Timelines and Budget).
  • Supports the Sr. Operational study lead in collaborating with clinical affairs and other functions, and responsible for, the execution and delivery of studies (e.g., Clinical Planning, Regulatory Affairs, Global Drug Safety, Pharmaceutical R&D, R&D Quality Assurance).
  • Responsible for the execution and adherence of various aspects of the study operational plan (start up, conduct, close-out, and vendor oversight) with input from key stakeholders including adherence to all relevant regulations including GCP, ICH and Regulatory requirements, as well as corporate SOPs and policies.
  • Responsible for monitoring assigned aspects of the study operational plan.
  • Responsible for managing assigned aspects of the operational study budget, timelines, and risk mitigation processes with input from key stakeholders.
  • Supports the development and application of standardized operational study processes, methodologies, appropriate quality and performance metrics and tools to systematize continuous process improvement and impart best practices across clinical operations to maximize its effectiveness.
  • Responsible for supporting the management and maintenance of the study TMF.
  • Supports the Sr. CTM in managing the selection, contracting and oversight of CROs and clinical trial related vendors in collaboration with the study team and key stakeholders.
 
Required Skills:
  • B.S. degree. Minimum of 3 to 5 years of pharmaceuticals/biotech experience.
  • Minimum of 3 to 5 years drug development experience in the pharmaceutical industry/CRO or commensurate clinical/medical research experience with emphasis on Phase II-IV clinical trials.
  • Process and system thinking, customer orientation, and ability to work in multidisciplinary study teams and to execute within a matrix management model, ideally in pharmaceuticals/biotech.
  • Experience in execution of clinical research trials, including GCP and regulatory guideline knowledge and audit inspections.
  • Knowledge and experience in clinical study budgeting including timeline and the application of clinical trial performance metrics.
  • Demonstrated ability to support the development and management of various aspects of the end-to-end study operational plan.
  • Demonstrated ability to support the operational execution and delivery of various aspects of a quality clinical trial.
  • Knowledge of drug development and FDA GCP/ICH regulatory guidelines.
  • Proficiency with and ability to utilize software applications that support Clinical Operations: Microsoft Word, Excel, PowerPoint; Adobe Acrobat, EDC systems, etc.
  • Strong ability to work within a matrixed organization, managing multiple tasks in a timely, budget conscious manner.
  • Ability to identify and work with key stakeholders to deliver operational requirements.
  • Ability to consistently operationalize abstract ideas.
  • Ability to identify issues, analyze situations and provide effective solutions.
  • Must possess demonstrated skill in the following: Decision-making, Judgment, and Problem Solving, Interpersonal relationships, team building, motivating, mentoring associates, and Influencing, Initiative and Accountability, Strong oral, and written communication skills.
  • Ability to embrace change and comfortable with ambiguity.
 
Preferred Skills:
  • Demonstrated experience in change management initiatives preferred.
  • Program and project management experience preferred .
  • Clinical trial management system (CTMS) background is a plus.
 
This 12+ month position starts ASAP.
 
Please E-MAIL your resume (attachment to email) with rate and availability to Bridget: bridget@alphaconsulting.com
 
ALPHA'S REQUIREMENT #21-03640
MUST BE ELIGIBLE TO WORK IN THE U.S. AS AN HOURLY W2 EMPLOYEE
#ZR
#LI-BB1
 

About the Company

Alpha Consulting Corp. logo

Alpha Consulting Corp.

Our goal, in addition to communicating the benefits of becoming associated with Alpha Consulting, is to provide news, opinions, and resources to assist Clients and Consultants. As with our careers, the content will continuously change and evolve over time.

Alpha Consulting Corporation is an IT (Information Technology) staffing business specialty with the ability to understand your specific project requirements and promptly supply appropriately matched consultants to fill both short and long-term client needs.

COMPANY SIZE
100 to 499 employees
INDUSTRY
Biotechnology/Pharmaceuticals
FOUNDED
1994
WEBSITE
http://www.alphaconsulting.com/