BSc Life Sciences Job Openings at Syneos Health as a Payment Support Specialist
Payment Support Specialist
Locations: IND-Hyderabad-Hybrid
Time type: Full time
Posted on: Posted 4 Days Ago
Job Requisition ID: 25100128
Payment Support Specialist
Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities.
Our Clinical Development model brings the customer and the patient to the center of everything that we do. We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to work with, but to make us easier to work for.
Whether you join us in a Functional Service Provider partnership or a Full-Service environment, you’ll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals. We are agile and driven to accelerate the delivery of therapies, because we are passionate to change lives.
Discover what our 29,000 employees, across 110 countries already know:
WORK HERE MATTERS EVERYWHERE
Why Syneos Health
We are passionate about developing our people, through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program.
We are committed to our Total Self culture – where you can authentically be yourself. Our Total Self culture is what unites us globally, and we are dedicated to taking care of our people.
We are continuously building the company we all want to work for and our customers want to work with. Why? Because when we bring together diversity of thoughts, backgrounds, cultures, and perspectives – we’re able to create a place where everyone feels like they belong.
Job Responsibilities
- Reviews and interrogates Clinical Trial Agreements (CTAs) and amendments to ensure payments align with documented costs, escalating discrepancies as needed.
- Attends, participates, prepares, and distributes meeting minutes and action items for internal and external meetings, following up 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, keeping IMS Leadership and Clinical Research Associates (CRAs) informed of site and study status.
- Ensures all study documents are archived according to guidelines and policies.
- Provides support for quality assurance activities, including audit preparation, documentation, and resolution of actionable issues.
- Works with sponsor systems and applications as required by the project.
Qualifications:
- 1 to 2 years of experience.
- Should have EDC, Data Management background.
- Associate’s Degree (or equivalent) level of qualification in life sciences, Medicine, Pharmacy, Nursing and 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.
- Ability to travel if necessary preferred (approximately 5%).
- High level of competence in English language.
Keywords: Please ensure you are subscribed to the Biotecnika Times Newsletter and our YouTube channel to be notified of the latest industry news. Follow us on social media like Twitter, Telegram, Facebo
