We have two openings for a Sr. Clinical Date Team Lead - one full time and one part time (20 hrs./ week). These contract roles, supporting West coast hours, imvolve leading complex clinical studies, mentoring teams, and serving as the primary clinical liason.
location: Telecommute
job type: Contract
salary: $52.20 - 58.00 per hour
work hours: 9 to 5
education: Bachelors
responsibilities:
- Applies relevant components of the project protocol to daily tasks and directs
others on how to apply to their daily tasks. - Acts as an interdepartmental and client liaison for all DM study activities.
- Produces project-specific status reports for management, Project Lead and/or
clients on a regular basis. - Monitors and analyzes study metrics and escalates per the organization's risk
management processes. - May participate in business development activities by assisting with bid
preparation and representing data management at bid defense meetings, where required. - Assists with project forecasting of hours and identification of resource
requirements. - Assists with the oversight of project budgets including identification of potential
out of scope work and participation in the Contract Modification process. - Leads, high volume/highly complex studies.
- Independently leads and delegates tasks to ensure timely completion of project
activities to project, quality and budget. - Mentors junior level staff on all associated tasks within a study.
- Assists with administrative and financial oversight for allocated projects.
- Communicates with management regarding all data management activities
within their studies.
qualifications:
- Bachelor's degree (BS) or equivalent and relevant formal academic / vocational qualification
- Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 5+ years).
- Ability to effectively apply knowledge and skills in a highly organized fashion while adhering to regulatory guidelines, SOPs and client expectations
- Ability to use interactive computer programs good written/ verbal communication skills with a strong command of English language and grammar; good organizational, analytical/problem solving skills and attention to detail
- Ability to work productively in both a team environment and independently as needed
- Ability to maintain a high degree of confidentiality with clinical data and client's proprietary data
- Ability to act as a study or department expert for DM processes
Ability to support project resourcing and project timeline planning and adherence to timelines
skills: CRF, CDISC, CRFs, Clinical Data Management, GCP (Good Clinical Practice), ICH Regulations, Good Clinical Practice (GCP), Veeva Vault
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: medical, prescription, dental, vision, AD&D, and life insurance offerings, short-term disability, and a 401K plan (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.
