Centralised Study Associate I
2 weeks ago
Support the payment of assigned studies which could include study set-up, maintenance, timely and accurate payment to the sites, as well as issue resolution and study reconciliation. Provide excellent customer service and site issue resolution Assist in setting entering study budgets and payees Review Electronic Data Capture updates and determine when certain budget items are payable Liaise with Site Agreements team to ensure timely receipt of site contracts, budgets and amendments Communicate with sites, Finance and clinical teams regarding payment questions and/or status updates Maintain and update payment tracking information Keep all study payments up to date and provide financial reports to study teams as requested Provide site payment documentation for sponsor audits as requested Generate investigative site payment reports for project team review (if applicable) Assist in the development and testing of enhancements to Grant Payment systems Contribute and participate in process Graduation/ Masters in Finance or Clinical 3 Years.
**Experience**
**Minimum Required**:
- 0-1 years transactional accounting (e.g. A/P, Billing, etc.), or relevant financial or clinical trial related experience
- Preferred:
- Working knowledge of clinical trial payment process and familiarity with investigator contracts and budgets; previous interaction with operational project teams and investigative sites preferred
- Strong networking abilities and an ability/willingness to work with internal and external stakeholders across the globe
- Strong analytical skills
- Good organizational and time management skills
- Excellent communication / writing skills
- Strong computer skills
- Computer proficiency (MS Office - Word, Excel, Power Point and Internet skills), aptitude for training
- Flexible and adaptable to a developing work environment
- Self-motivation with the ability to work under pressure to meet deadlines
- Works well independently as well as in a team environment
- Detail and process oriented
- Positive attitude and approach
- Customer oriented
**Education**:
University/College degree (Business or Accounting preferred) AND three 0-1 years work experience in a financial, clinical trial, or grant payment position.
Strong computer skills with an ability to understand, access and leverage technology alternatives
**Labcorp is proud to be an Equal Opportunity Employer**:
As an EOE/AA employer, Labcorp strives for diversity and inclusion in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications of the individual and do not discriminate based upon race, religion, color, national origin, gender (including pregnancy or other medical conditions/needs), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. We encourage all to apply.
For more information about how we collect and store your personal data, please see our Privacy Statement.
-
Centralised Study Associate I
2 weeks ago
Bengaluru, India Labcorp Full timeFollow all applicable departmental Standard Operating Procedures and Work Instructions. Complete required trainings according to required timelines. Complete day-to-day tasks ensuring quality and productivity. Maintain project and technical documentation in an appropriate manner. Perform checks to ensure quality of work completed Ensure timely escalation as...
-
Centralised Study Associate I
3 days ago
Bengaluru, India Labcorp Full timeFollow all applicable departmental Standard Operating Procedures and Work Instructions. Complete required trainings according to required timelines. Complete day-to-day tasks ensuring quality and productivity. Maintain project and technical documentation in an appropriate manner. Perform checks to ensure quality of work completed Ensure timely escalation as...
-
Study Start Up Associate I
2 weeks ago
Bengaluru, Karnataka, India ICON Plc Full timeSSUA I, Bangalore, Office based 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 We are currently seeking a Study Start Up Associate I to join our...
-
Centralized Study Spec I
2 weeks ago
Bengaluru, Karnataka, India Fortrea Full timeAs 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. Conducting operations in...
-
Centralized Study Associate I
2 weeks ago
Bengaluru, India Labcorp Full timePosition provides process, control, coordination, and approval of clinical trial documents. Position is responsible for ECD, Phase I-IV electronic trial master file (eTMF). ¨ Maintains an understanding of applicable regulatory requirements. ¨ Managing electronic Trial Master Files (eTMF), (Trial, Country and Site artifacts) for clinical studies in...
-
Reporting Associate I
2 weeks ago
Bengaluru, India Labcorp Full timeThe statements below reflect the general responsibilities and requirements of the identified position but may not describe all the work requirements that may be inherent in the job. **Job Summary**: **Essential Job Duties**: - The Reporting Associate I learns and performs the duties of drafting and finalizing nonclinical study reports and completes the...
-
Centralized Study Associate I
2 weeks ago
Bengaluru, India Labcorp Full timeTo complete Other duties/activities as assigned by study management team, but not limited to: Manage clinical systems & access management Manage study documents such as study level, country level and site level Maintain study databases (CTMS, IWRS, EDC etc.) Support study team in e-TMF management activities Support study team in data review and support...
-
Drug Safety Associate I
7 days ago
Bengaluru, India Novo Nordisk Full timeDrug Safety Associate I Drug Safety Associate I Drug Safety Associate I
-
Study Start Up Associate I
3 days ago
Bengaluru, Karnataka, India Icon plc Full timeStudy Start Up Associate I - India, Bangalore Hybrid: Office based 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 At ICON, it’s our people...
-
Pre Sales Associate
1 week ago
Bengaluru, India upGrad Study Abroad Full timeJob Overview : We are seeking a passionate Study Abroad Counsellor to assist students in pursuing their Study Abroad goals, with a focus on Global education market opportunities. You'll guide students through the application process, Offer Expert advice on Universities, Courses, Visa and Scholarships, and support them throughout their...