Job Opportunity - Drug Substance (Viral Vaccine Experience) Bharat Biotech is looking for skilled professionals with hands-on experience in Drug Substance manufacturing for Viral Vaccines. Details are provided below 1. Location: Hyderabad 2. Experience: 2-6 Years 3. Key Skills & Experience Required a. Experience in Upstream /Downstream Processing of viral vaccines b. Operation and handling of bioreactors, fermenters, centrifuges, chromatography systems, filtration units c. Knowledge of cell culture techniques (mammalian/avian cell lines) d. Familiarity with aseptic techniques, GMP documentation, batch records e. Understanding of process optimization, scale-up, and technology transfer f. Exposure to in-process testing, troubleshooting, and equipment cleaning/sterilization g. Ability to work in a regulated, fast-paced manufacturing environment 4. How to Apply Interested candidates can share their updated CV to kiran4978@bharatbiotech.com Mention subject line as: Appl...
Syneos Health Requires
Payment Support Specialist
Location: India-Asia Pacific - IND-Home-Based, India
Job ID: 24004943
Description
Syneos Health is a fully integrated biopharmaceutical solutions organization purpose-built to accelerate customer success. They lead with a product development mindset, seamlessly connecting capabilities to add high-value insights to speed therapies to patients and provide practical value to help customers achieve their objectives.Company's Clinical Development model brings the customer and the patient to the center of everything . They are continuously looking for ways to simplify and streamline their work to not only make Syneos Health easier to work with, but to make them easier to work for.
Job Description (Payment Support Specialist)
JOB SUMMARY
The Project Specialist performs administrative and supportive activities assigned by the Manager, IMS or designee to ensure the contracted services and expectations are carried out by the IMS team in accordance with executed contracts and the customers’ expectations.
JOB RESPONSIBILITIES
- Reviews and interrogates Clinical Trial Agreements (CTAs) and CTA amendments to ensure payments are being approved according to the documented costs.
- Discrepancies should be escalated to their line manager, or the appropriate team member as needed.
- Attends, participates, prepares and distributes meeting minutes and action items for both internal and external meetings (sponsor, trusted process, functional, investigator meetings).
- Follows up with team members on action items to closure.
- Collaborates with clinical operations, project management, accounts payable, accounts receivable, and site contracts teams.
- Maintains timely and effective communication among team members and site staff.
- Keeps IMS Leadership and Clinical Research Associates (CRAs) fully appraised of sites and study status.
- May contact site staff as needed for critical information.
- Ensure all study documents are archived based on the appropriate guidelines and policy.
- Provide support for quality assurance activities, including preparation for audits and internal review, prepare documentation and follow through to resolution on actionable issues.
- Works with sponsor systems and applications as required by the project.
QUALIFICATION REQUIREMENTS
- Any life sciences, Medicine, Pharmacy, Nursing or related field or equivalent combination of education and experience.
- Knowledge of Good Clinical Practice/ICH guidelines and other applicable regulatory requirements.
- Strong organizational skills.
- Ability to manage time and work independently.
- High proficiency with full MS Office Applications.
- Strong communication, presentation, interpersonal skills, both written and spoken, with an ability to inform, influence, convince, and persuade
- High level of competence in English language
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