Trial Patient Payment Associate Iii

2 weeks ago

Mumbai, Maharashtra, India Thermo Fisher Scientific Full time
At Thermo Fisher Scientific, you'll discover meaningful work that makes a positive impact on a global scale.

Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer.

We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies.

With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services.

Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on - now and in the future.


Our goal-driven teams combine and deliver centralized support and solutions for the clinical trials, collaborating to improve processes, cycle and flexibility.

We partner with our sites, businesses and colleagues around the world to decrease startup timelines and exceed expectations.

  • Discover Impactful Work:


Provides senior administrative, reporting, contractual and financial support to the department related to the processing of payments to investigative sites.

Responsibilities include data compilation, issue/risk resolution, ensuring adherence to contractual guidelines and country regulations, and providing training and guidance to junior team members.

Compile data from multiple sources to generate payments to sites in accordance with procedural documents and site contracts.

  • A day in the Life:
  • Ensures adherence to country-specific regulations which affect and impact ability to pay. Manages payment responsibilities and workflow to meet contracted timelines and project deliverables.
  • Builds and leads relationships with study sites and interface, on occasion, with clients for paymentspecific issues.
  • Responds to studyrelated escalations and resolves paymentrelated findings. Raises project risks appropriately.
  • Trains study teams on site payment processes, including setting expectations around site payments' requirements and deliverables.
  • May process investigator payments in middleware and financial system; manage refunds, credit notes, late payment fees, prepayments or investigator meeting reimbursements.
  • May build and enter budgets and SVTs; work on transparency reporting; perform study reconciliations; lead and maintain investigator funds tracker for studies transitioned to site payments.
  • As a senior team member, assists in providing training, guidance, and review to junior team members.
  • Keys to Success:

Education

  • High / Secondary school diploma or equivalent and relevant formal academic / vocational qualification / Bachelor's degree preferred Technical positions may require a certificate.

Experience

  • Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to at least 6 years).
  • In some cases an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role.

Knowledge, Skills, Abilities

  • Strong organizational skills and strong attention to detail
  • Proven ability to handle multiple timeline sensitive tasks efficiently and effectively
  • Flexible and able to reprioritize workload to meet changing project needs
  • Strong computer skills, proficient in MS Word and Excel; preferred experience using CTMS, EDC, or financial systems
  • Capable of working independently and as a team member, promoting strong team approach and serving as a role model to others
  • Effective communication skills, which includes English language (oral, written) and other languages would be an advantage (where applicable)
  • Demonstrated ability to extract pertinent information from study documentation such as protocol, contracts, budgets, etc. and perform applicable data entry of said documents
  • Strong ability to effectively analyze project specific data/systems to ensure accuracy and efficiency
  • Good understanding of ICH Good Clinical Practices, Country Regulatory and/or applicable tax regulations, etc. for all nonclinical/clinical aspects of project implementation, execution, and closeout
  • Capable of mentoring and training junior team members
  • Demonstrated ability to effectively analyze project specific data/systems to ensure accuracy and efficiency
  • Working EnvironmentThermo Fisher Scientific values the health and wellbeing of our employees. We support and encourage individuals to create a healthy and balanced environment where they can thrive.
Below is listed the working environment/requirements for this role:

  • Able to communicate, receive, and understand information and ideas with diverse groups of people in a comprehensible and reasonable manner.
  • Able to work upright and stationary for typical working hours.
  • Ability t

  • Trial Patient Payment Associate III

    2 weeks ago

    Mumbai, Maharashtra, India Thermo Fisher Scientific Full time

    include data compilation, issue/risk resolution, ensuring adherence to contractual guidelines and country regulations, and providing training and guidance to junior team members. Compile data from multiple sources to generate payments to sites in accordance with procedural documents and site contracts. A day in the Life: Ensures adherence to...

  • Trial Patient Payment Associate Ii

    2 weeks ago

    Mumbai, Maharashtra, India Thermo Fisher Scientific Full time

    At Thermo Fisher Scientific, you'll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through...

  • Clinical Trial Associate

    2 weeks ago

    Mumbai, Maharashtra, India Ortolan Full time

    Clinical Trial Associate Mumbai or Vadadora, India (hybrid: 3 days office, 2 days home) Salary: Competitive + Benefits + Bonus If you are an agile, committed, and innovative clinical trial professional then we want to hear from you Join us to help improve peoples' lives and make healthcare better for everyone Why Pharmanovia? Pharmanovia is...

  • Clinical Trial Associate

    2 weeks ago

    Mumbai, Maharashtra, India Atnahs Full time

    Mumbai or Vadodara, India (hybrid: 3 days office, 2 days home):Salary:Competitive + Benefits + Bonus:If you are an agile, committed, and innovative clinical trial professional, then we want to hear from youJoin us to help improve peoples' lives and make healthcare better for everyoneWhy Pharmanovia?:Pharmanovia is a dynamic, fast-growing international...

  • Trial Master File Associate

    2 weeks ago

    Mumbai, Maharashtra, India BIORASI LLC Full time

    We are Growing Let us support your career journey the Biorasi way. Innovative, Collaborative, Dynamic and Evolving. Capitalizing on your strengths while encouraging work-life balance. Biorasi is an award-winning, customer-focused, full-service clinical research organization, and we are unlike any CRO you've ever heard of.Biorasi is looking for top performers...

  • Clinical Trial Assistant

    2 weeks ago

    Mumbai, Maharashtra, India ICON Strategic Solutions Full time

    ICON plc is a leading healthcare intelligence and clinical research company. We take pride in creating a diverse and innovative work environment, and we invite you to be part of our journey to influence the future of clinical development.Clinical Trial AssistantLocation : Mumbai, On-siteResponsibilities:- Document collection and submission support- Vendor...

  • Clinical Trial Assistant

    2 weeks ago

    Mumbai, Maharashtra, India ICON Strategic Solutions Full time

    ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development. Clinical Trial Assistant Location : Mumbai, Office based Responsibilities: What you will be...

  • Patient Coordinator

    2 weeks ago

    Mumbai, Maharashtra, India ACME HOSPITAL Full time

    JOB LOCATION WILL BE CHEMBURGreeting and directing patients to examination rooms. Scheduling patient appointments and making reminder calls. Informing patients about delays and waiting times. Obtaining patients' Basic details for registration in software. Assisting patients in filling out patient history forms, consent forms, and payment contract forms, when...

  • SAS/PH- Clinical trial analysis

    2 weeks ago

    Mumbai, Maharashtra, India Anicalls (Pty) Ltd Full time

    Excellent understanding of the statistical principles underlying clinical trials Excellent statistical skills. candidates that are Statistical SAS, R programmers, and separately, we need pharmaceutical clinical trial statisticians. Excellent understanding of the regulatory issues associated with the reporting of clinical data in the submission process

  • Clinical Research Associate

    2 weeks ago

    Mumbai, Maharashtra, India Novo Nordisk Full time

    Department: Clinical Development CentreDo you want to be a part of a high performing team in Novo Nordisk that plays a critical role in driving the success of the business? Do you have what it takes: the right drive, a sharp mind, customer orientation, openness and focus on what matters and a genuine interest in working with people? If you find challenges...

  • Program Associate- CFBE

    2 weeks ago

    Mumbai, Maharashtra, India SPJIMR SP Jain Institute of Management & Research Full time

    *Request you to go consider going through the JD before applying*The Program Associate for CFBE will be responsible for coordination and management of all administrative processes involving students, professors and other SPJIMR administrative staff for a particular phase/batch assigned in the CFBE Program.About CFBE Program:SPJIMR Centre for Family Business...

  • Clinical Trial Administrator

    2 weeks ago

    Navi Mumbai, Maharashtra, India Labcorp Full time

    Essential Job Duties:1) Document and track study activities using relevant forms and tools, as well as relevant Project Management Systems with guidance/support2) Assist in the preparation of study and site specific materials in accordance with relevant SOPs3) Complete minute taking and documentation for sponsor/external or internal teleconferences as...

  • Patient Relation Executive

    2 weeks ago

    Mumbai, Maharashtra, India SRV Hospital Full time

    Urgent Opening For Resident Medical Officer In NICU Department At SRV Hospital, Chembur. Department Patient Relation (Front Desk) Qualification Graduation Experience 1 To 5 Years (Healthcare Industry)Job Description Undertake duties in accordance with departmental policies and procedures To be fully conversant in all areas of Front Office Meet and greet...

  • Program Associate- CFBE

    2 weeks ago

    Mumbai, Maharashtra, India SPJIMR SP Jain Institute of Management & Research Full time

    *Request you to go consider going through the JD before applying*The Program Associate for CFBE will be responsible for coordination and management of all administrative processes involving students, professors and other SPJIMR administrative staff for a particular phase/batch assigned in the CFBE Program.About CFBE Program:SPJIMR Centre for Family Business...

  • Medical Advisor

    2 weeks ago

    Mumbai, Maharashtra, India Abbott Laboratories Full time

    MAIN PURPOSE OF ROLE Experienced professional individual contributor that works under limited supervision.MAIN RESPONSIBILITIES: As the Experienced professional in the Medical Affairs Sub-Function, possesses well developed skills in overseeing the direction, planning, execution, clinical trials/research and the data collection activities. Contributes to...

  • Clinical Research Associate

    2 weeks ago

    Mumbai, Maharashtra, India REGROW BIOSCIENCES Full time

    About the company and the position:Hey there! Are you a Clinical Research Associate (CRA) looking for an exciting opportunity to be a key player in clinical trials? Well, look no further! Join our team and be a crucial part of the development and execution of cutting-edge clinical research. Here's what you'll be doing:Responsibilities: Assist in developing...

  • Lead Payment Analyst

    2 weeks ago

    Mumbai, Maharashtra, India Johnson and Johnson Full time

    Global Clinical Operations (GCO)Lead Analyst, Payments (CCS) Position Summary: Responsible for the management of the end-to-end investigator/site payment processes and payment calculations, creation and management of purchase orders, payment and clinical trial payments.Acts as liaison among colleagues within Contract & Centralized Services (CCS) and study...

  • Clinical Research Associate

    2 weeks ago

    Mumbai, Maharashtra, India REGROW BIOSCIENCES Full time

    Overview:As a Clinical Research Associate (CRA), you will play a pivotal role in the development and execution of clinical trials Working closely with research teams, regulatory bodies, and clinical sites, you will ensure compliance with protocols, regulatory requirements, and industry standards throughout the trial processResponsibilities:1 Trial...

  • Clinical Data Associate

    2 weeks ago

    Mumbai, Maharashtra, India Fortrea Full time

    As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. With over 19,000 staff...

  • CRA Manager

    2 weeks ago

    Mumbai, Maharashtra, India Novo Nordisk Full time

    The position This role requires someone to Coordinate, in partnership with the COM (Clinical Operation Manager) and CDC-TM (Trial Managers), the clinical trial set-up at a local level to ensure appropriate site and resources allocation. Manage local clinical projects, ensuring they are executed in a timely and effective manner, within budget and complying...