As the largest staffing and recruitment agency in the world, we can commit to finding you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. We supply prestigious life sciences and biopharma companies with job seekers like you to achieve their business goals. If you're looking for a position where you can serve as an asset to your company while making a difference in others' lives, we have the ideal position for you!
location: Aliquippa, Pennsylvania
job type: Contract
salary: $70.00 - 83.88 per hour
work hours: 9 to 5
education: High School
responsibilities:
- Accountable for quality delivery and competencies within the eCOA service area
- Oversee study level system requirements meetings with eCOA vendors and internal stakeholders
- Assist in the design and development of study specific technical documents
- Support the internal team in managing project related timelines and associated activities
- Partner with data management (DM) to define the requirements for data transfers
- Work with external resources to manage the creation and execution of user acceptance tests
- Identify and track study-related technical issues to resolution
- Provide a supportive framework for continuous process and quality improvements
qualifications:
Basic Qualifications:
- Doctorate Degree OR
- Master's Degree and 3 years of Clinical experience OR
- Bachelor's Degree and 5 years of Clinical experience OR
- Associate degree and 10 years of Clinical experience OR
- High school diploma/GED and 12 years of Clinical experience
- Bachelor's Degree in life science, computer science, engineering, business or related discipline
- 4+ years of experience in clinical development
- Experience implementing clinical systems, such as CTMS, EDC, IVRS, ePRO or other related technology in the pharmaceutical/biotechnology industry
- Knowledgeable in Good Clinical Practices, and FDA regulations necessary
- Project management and technical expertise, attention to detail, and excellent documentation and communication skills
- PMP
- Previous vendor management experience
- Excellent time management and organization skills
- Have sound problem resolution, judgment, and decision-making abilities
- Be able to work well in a team-based environment with minimal supervision
skills: FDA, GCP (Good Clinical Practice), PMP, CTMS, CTMS (Clinical Trial Management Systems), TMF
Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.
At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact HRsupport@randstadusa.com.
Pay offered to a successful candidate will be based on several factors including the candidate's education, work experience, work location, specific job duties, certifications, etc. In addition, Randstad offers a comprehensive benefits package, including health, an incentive and recognition program, and 401K contribution (all benefits are based on eligibility).
This posting is open for thirty (30) days.
It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.
