Job Title: Clinical Research Associate
Department: QA Clinical
FLSA Status: Exempt
Position Overview
The Clinical Research Associate is responsible for supporting clinical activities for domestic and international studies as well as support other related initiatives, as required.
Responsibilities
Minimum Requirements:
Compensation & Benefits:For U.S.-based positions only, the annual base salary range for this role is $87,800.00 - $131,675.00This position may also be eligible for incentive compensation.We offer a comprehensive benefits package, including:
We are looking for highly motivated, performance-driven individuals to be a part of our expanding team. We do this by hiring amazing people guided by shared values who exceed customer expectations. Our continued success depends on it!
At Insulet Corporation all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.
(Know Your Rights)
Department: QA Clinical
FLSA Status: Exempt
Position Overview
The Clinical Research Associate is responsible for supporting clinical activities for domestic and international studies as well as support other related initiatives, as required.
Responsibilities
- Collaborate with team members in the evaluation and establishment of clinical study sites by performing site qualification visits to ensure applicability of sites for planned study.
- Collaborate with Senior Clinical Research Associate to create source documentation/CRFs in alignment with protocol requirements.
- Create consent and assent templates specific to the needs of the planned study.
- Collaborate with sites and internal stakeholders to align and implement site specific language for each consent/assent.
- Train site staff on protocol requirements, source documentation, and case report form completion.
- Serve as the primary liaison with Institutional Review Board (IRB) in the preparation and submission of all study related documentation including but not limited to the study protocol, consent/assent, user guides, training presentations, Curriculum Vitaes (CVs), licenses, and study amendments.
- Conduct regular monitoring visits to ensure study protocol compliance, primary data collection is recorded properly, and appropriate reporting is being conducted.
- Coordinate project meetings.
- Participate in the creation and review of clinical study reports for regulatory submission ensuring alignment of all the critical report elements such as adverse events, device deficiencies, etc.
- Participates in team meetings and tracks action items.
- Ensure compliance with SOPs and local regulations, and ICH and GCP guidelines.
- Performs other duties as required.
Minimum Requirements:
- B.S. or B.A. and/or an equivalent combination of education or experience.
- CRA certification
- Minimum of 3 years of experience.
- Available to travel on short notice and independently manage travel schedules.
- Direct experience in participating in the execution of clinical research studies.
- Must have analytical skill, be detail oriented and have good interpersonal skills.
- Knowledge of agency guidelines and requirements.
- Excellent written and effective verbal communication skills.
- Ability to communicate at all levels of an organization.
- PC skills; word processing, spreadsheet, database, Internet search and utilization.
- Flexible and able to work in a fast-paced environment.
- Team player.
- Ability to organize and judge priorities.
- Excellent ability to generate and maintain accurate records.
- None.
Compensation & Benefits:For U.S.-based positions only, the annual base salary range for this role is $87,800.00 - $131,675.00This position may also be eligible for incentive compensation.We offer a comprehensive benefits package, including:
- Medical, dental, and vision insurance
- 401(k) with company match
- Paid time off (PTO)
- And additional employee wellness programsApplication Details:This job posting will remain open until the position is filled.To apply, please visit the Insulet Careers site and submit your application online.Actual pay depends on skills, experience, and education.
We are looking for highly motivated, performance-driven individuals to be a part of our expanding team. We do this by hiring amazing people guided by shared values who exceed customer expectations. Our continued success depends on it!
At Insulet Corporation all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.
(Know Your Rights)