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Clinical Research Specialist Jobs
Company | Össur |
Address | , Irvine |
Employment type | FULL_TIME |
Salary | |
Expires | 2023-12-13 |
Posted at | 8 months ago |
locations
Irvine, California, USA
time type
Full time
posted on
Posted 2 Days Ago
job requisition id
REQ-2974
Works as part of the Medical Office team to create and maintain clinical documents as a part of a medical device technical file. Identify, accumulate, review and appraise clinical data from published literature and databases. Manage clinical studies of products from creation through testing and finalizing with written summaries. Collaborates with teams from R&D, marketing, and global product management.
Responsibilities:
- Research protocols
- Institutional Review Board Documents
- Teamwork
- Function as part of a team to meet product goals and timelines
-
- Clinical trial outcome reports
- Function as part of a team to meet product goals and timelines
- Clinical Research
- Design and implement internal clinical research. This includes both qualitative and quantitative research
-
- Design and implement internal clinical research. This includes both qualitative and quantitative research
- Draft and review clinical content in other Product Information
- Clinical evaluation reports
- Literature reviews
- Medical Writing
- Literature reviews
- Clinical evaluation reports
- Research protocols
- Clinical trial outcome reports
- Institutional Review Board Documents
- Draft and review clinical content in other Product Information
-
General:
- All training related to the quality management system is done in accordance to the Training Management Process.
- Contributes to a safe working environment by maintaining own workspace and reporting any potential hazards.
- All employees must be aware, have knowledge and shall have received general training in Quality requirements of Össur. Training takes place in the Onboarding process and in New Employee Orientation. More specific Quality training is job specific.
- Exercises good use of company funds and property within the set guidelines. Maintains an honest and professional attitude as the company’s representative at all times.
Qualifications:
- Medical writer qualifications or Certified Research Associate a plus
- Strong collaborative and teamwork skills
- Bachelor’s degree in engineering and/or life sciences and/or qualified health care professional (i.e Certified Orthotist, Physical Therapist, Occupational Therapist, Athletic Trainer, Nurse)
- Good presentation/communication skills
- Experience with both qualitative and quantitative research a plus
- Exceptional time management skills
- Proficient in MS Office applications: Word, PowerPoint, Excel
- 2+ years experience with a documentation for regulatory compliance of medical devices, clinical research, project management preferred
The US base salary range for this full-time position is $81,356 -$116,270 + bonus + benefits. Our salary ranges are determined by role, level, and location. The range displayed on each job posting reflects the minimum and maximum target for new hire salaries. Within the range, individual pay is determined by work location and additional factors, including job-related skills, experience, and relevant education or training. Your recruiter can share more about the specific salary range for your preferred location during the hiring process.
Please note that the compensation details listed in US role postings reflect the base salary only, and do not include bonus, equity, or benefits.
Benefits we offer:
- Affordable Accidental and Critical Illness Insurance
- Wellness Program - Save up to 30% in your medical premiums
- 10 Paid holidays
- Referral Bonuses
- 401(k) plan with company match
- We provide a flexible work environment to offer work/life balance
- Company Paid Life Insurance
- Annual Performance Reviews
- And Much More…
- Tuition Reimbursement
- Affordable Short- & Long-Term Disability Insurance
- Medical, dental, and vision insurance
- Give Back Program – Paid time off to Volunteer
- Paid Sick and Vacation time
Össur is an Equal Opportunity/Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex including sexual orientation and gender identity, national origin, disability, protected Veteran Status, or any other characteristic protected by applicable federal, state, or local law.
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