Clinical Trials Manager Jobs in Springfield, NJ (NOW HIRING)

Artech is the 10th Largest IT Staffing Company in the US, according to Staffing Industry Analysts' 2012 annual report. Artech provides technical expertise to fill gaps in clients' immediate skill-sets availability, deliver emerging technology skill-sets, refresh existing skill base, allow for flexibility in project planning and execution phases, and provide budgeting/financial flexibility by offering contingent labor as a variable cost.

Job Description:
$124,500 with a 12 to 15% bonus
Job Description Accountabilities:
Sets objectives, delivers results and implements policies and operational targets that have a direct impact on the work unit or operational outcome
Work may include policy changes or recommendations
Individual contributor with specialized knowledge
Has an easily discernible impact on the job area and expected results
Typically no cost center budget management responsibility
Complexity / Innovation:
Executes work procedures in a project context. Consistently exercises judgment and discretion within generally defined procedures
Technical expert with sufficient expertise and experience to be considered for sensitive or complex assignments
Called upon to develop solutions utilizing creativity and ingenuity
Communication:
Presents concepts, facts, and reports to mid-level internal and external clients to advise of key trends and issues
Contact with clients and external vendors and troubleshooting routine client inquiries. May represent the organization as a prime contact for technical matters of significant complexity
Supervision Given / Received
Directs the activity of a work team project within the department. May have responsibility for management of highly skilled professional employees
Work is completed under limited supervision
Typically reports to an Associate Director or above
CDP Development and Management:
Supports the planning, execution and reporting of clinical programs/ trials
Clinical Research Protocols
Reviews Clinical Protocols
Study Management
Reviews study documents (i.e., investigator databases, ICFs, IEC/ IRBs submissions)
Clinical Research Expert
Contributes to risk resolution by escalating and monitoring projects risks
Resource Management
Makes recommendations for improving resources (tools, systems, vendors, etc.) needed by the team
Manages the workflow of others to ensure work is done within a given deadline
May manage contractors and ensure that contractors, consultants and vendors complete assigned work according to agreed timelines
Financial Management:
Tracks the expenses of work teams to anticipate cost issues
Manages the use of financial standards, guidelines and compliance for more informed and empowered decisions
May assist the review of 3rd party (contractors, consultants and vendors) work product and deliverables to recommend approval of payment of invoices or escalate issues when appropriate
Matrix and Team Management:
Provides feedback, sets clear tasks and objectives and coaches team members on a periodic basis
May support employees by providing input into recruitment, selection, performance, succession, and transition activities
Trains team members on processes and / or systems
People Management (if assigned direct reports):
Manages individual contributors
- Manages all employee-related activities throughout the year, including performance management and development
- Identifies and communicates the skills, behaviors and experiences required to develop employees
- Sets goals, reviews performance and provides feedback on a regular basis
Assists or Leads training of junior staff
Compliance:
Complies with all applicable laws / regulations of each country in which we do business
Demonstrates high ethical behavior at all times, whether dealing with colleagues, vendors, patients, or physicians
Reports legal, compliance and ethical violations in a timely manner
Qualifications and Experience:
- MS or PhD
- Experience in Clinical Research methods and processes required.
- Previous experience with Oncology Clinical Research studies is required. Position requires attention to detail, and medical knowledge would be beneficial.
Foundational knowledge in:
- Clinical Trial Design and Execution.
- Clinical Development Planning.
- Regulatory Management.
Job Qualifications Qualifications and Experience
- MS or PhD
- Experience in Clinical Research methods and processes required.
- Previous experience with Oncology Clinical Research studies is required. Position requires attention to detail, and medical knowledge would be beneficial.
Foundational knowledge in:
- Clinical Trial Design and Execution.
- Clinical Development Planning.
- Regulatory Management.

Bachelor degree or above in scientific or related field Minimum 5-7 years experience in Data Management with experience in managing projects, project teams. Experience with In-Form or other EDC software is desirable however, should have some experience in supporting Oncology studies. Must be able to work independently. Proficiency on all related regulations, GCP, and Good Clinical DM Practice. Project management skills required. Strong oral and written communication skills. - Leadership skills a must

Best Regards,

Anuj Mehta

973-967-3402