Regulatory Affairs Associate - Publisher
at Parexel
Desde casa, Río Negro, Argentina -
Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
---|---|---|---|---|---|---|---|
Immediate | 20 Sep, 2024 | Not Specified | 21 Jun, 2024 | N/A | Interpersonal Communication,Biotechnology,English,Biochemistry | No | No |
Required Visa Status:
Citizen | GC |
US Citizen | Student Visa |
H1B | CPT |
OPT | H4 Spouse of H1B |
GC Green Card |
Employment Type:
Full Time | Part Time |
Permanent | Independent - 1099 |
Contract – W2 | C2H Independent |
C2H W2 | Contract – Corp 2 Corp |
Contract to Hire – Corp 2 Corp |
Description:
An Associate must have a knowledge of the organization´s basic consulting models and methodologies as well as basic knowledge of what services the department provides. An Associate must be technically competent and continually developing the skills as defined in the department, under general direction of his/her Line Manager and Supervisor, taking responsibility for ensuring that client work is performed and delivered on time, meeting the quality expectations based on Processes of the department and client preferences.
SKILLS:
- Autonomy and proactivity organized knowing how to prioritize and plan.
- Interpersonal communication.
- Client focus, results orientated,
- Flexibility to work in different scenario.
MINIMUM WORK EXPERIENCE:
- Initial years of experience in an industry-related environment.
- Preference Regulatory knowledge, ICH Guidance.
EDUCATION:
- Scientific (Pharmaceutical, Biochemistry, Biotechnology, others) or Technical Discipline (Translator, IT)
LANGUAGE SKILLS:
- Fluent verbal and written English.
Responsibilities:
- Shift: from 2 pm to 10.30 pm Argentina time with 30 minutes break
- Works effectively within a team environment, reporting to his/her LM and Supervisor.
- Works within broad project guidelines as directed by Line Manager.
- With the guidance of the Supervisor and Manager, demonstrates the ability to prioritize work to achieve specified project outcomes.
- Under supervision provides electronic publishing services, including preparation of submission packages, bookmarking, hyperlinking, compilation among others.
- Under supervisor performs basic document management task including file transfer, storage, tracking and archival.
- Capitalizes on opportunities to improve one´s own performance and seeks feedback from Manager,
- Supervisor, and colleagues. Applies information provided by Manager or supervisor to complete assigned project activities.
- Produces quality work that meets the expectations of the department based on process and client needs.
- May serve as client facing role for publishing submissions.
- Identify and escalate issues to upper management for a quick resolution based on process and client needs.
- Ensures that the tasks received are done with quality.
- Work and prepare in trainings of New Regulations that will help to the global team.
- Prepares planners, forms, and covers for specific projects.
- Understands ICH Regulations and Health Authorities regulations that impact in his / her daily work
REQUIREMENT SUMMARY
Min:N/AMax:5.0 year(s)
Information Technology/IT
Pharma / Biotech / Healthcare / Medical / R&D
Software Engineering
Graduate
Proficient
1
Desde casa, Argentina