Job Name: Clinical Trial Specialist (SSU - Russia
Job Description:
"Primarily contribute to the Dept. portfolio centralized support enhancement and process optimization, mainly focusing on the central enhancement to the human genetic resource (HGR) application and approval related for across Therapeutical Areas in line with company’s requirements and business needs and/or site GCP center submission and IEC submission preparation and submission and follow up.
As a Mentor of junior roles, such as Clinical Trial Assistant and Clinical Trial Specialist.
Collaborate with Local Trial Manager and Site Manager to ensure optimal management of all documents.
Ensures trial related activities are following company’s policies, SOPs, and local HA requirements, as well as other requirements, if applicable."
Designation:
None
Name of Organization:
Jhonsons and Jhonsons
Job Market In The Country:
Healthcare Staffing Market size was valued at USD 42.67 Billion in 2021 and is projected to reach USD 81.82 Billion by 2030, growing at a CAGR of 7.5% from 2023 to 2030.
Salary and Benefits:
Company also provides medical and surgical coverage and support for employees, global parental leave, in the case of a natural disaster, receive their full pay for up to three years and a continuation of benefits, The Energy for Performance® program teaches employees how to manage and expand their energy capacity to perform at their personal best in all areas of their lives, Employees can take the course either virtually from their remote office or in the classroom at company locations worldwide, in 17 language.
Refer to official website for Salary and more information.
Taxes and Financial Implications:
Taxable income amount subject to cumulative withholding (RMB) : 36,000 - 144,000
Withholding rate : 10%
Quick deduction ( RMB) : 2,520
Language Requirements:
Proficient in English language.
Eligibility Criteria
"Education and Experience Requirements:
(Describe the minimum knowledge, skill and ability requirements for the position. Include any degrees or certifications which are required and/or desirable.)
• Bachelor's degree or equivalent required, preferably in Clinical Medical, Pharmacy, Biochemistry, etc.,
• Minimum of 6 years of clinical research experience acquired in pharmaceutical industry, CRO or investigational site.
• Strong therapeutic area knowledge and/or operational experiences in assigned therapeutic area(s).
• Effective communication and solid decision-making skills.
• Effective issue resolution and ability to generate and implement contingency plans for both productivity and quality issues when required. Excellent knowledge of drug development, clinical research operations and regulatory requirements including ICH-GCP, HCC and applicable regulations.
• Ability to synthesize and evaluate data generated from various reports and sources.
• Flexible mindset and ability to work in a fast-changing environment. Operates under limited supervision.
• Proficient in English language. Computer literacy. Strong interpersonal and negotiating skills. Excellent organizational skills and the ability to collaborate and handle multiple priorities within a matrix environment. Perform activities in a timely and accurate manner."