8 Clinical Domain Jobs

Must have skillset 4-6 years of hands-on experience with Oracle/SQL Good knowledge and experience of SQL (Strong in SQL & PL/SQL) Experience on any of the ETL tools Hands-on experience in any Test Management tools like HP ALM or Synapses RT and Jira Should possess strong knowledge in ETL concepts Strong knowledge in SDLC/STLC processes, along with Testing Concepts Candidate should have knowledge about Test Plan/Test Strategy or any test deliverable documents Knowledge about Defect Life Cycle Should have analytical skill Candidates must have strong verbal, written, and communication skills Good to have skillset – Experience with Clinical data/Clinical Domain Agile and Lean SDLC process Experi...

As a Sr Statistical Programmer at Syneos Health, you will play a crucial role in developing programs and providing statistical programming support. Your main responsibilities will include: - Having 5+ years of experience in Advanced SAS/R programming and SQL - Experience in R programming, R Package development, and good knowledge of SQL - Hands-on knowledge of Python will be considered valuable along with R programming - Understanding of TIBCO Spotfire visualization tool or equivalent, and creating calculated columns, markings, filtering, and document properties - Knowledge or hands-on experience in Clinical domain and drug development process (Phase I through IV), Clinical Data Management -...

As a Veeva Config Specialist, your role will primarily involve focusing on Veeva Vault Configurations in the life sciences sector. Your key responsibilities will include: - Having 5-8 years of experience in the life sciences sector, with a strong emphasis on Veeva Vault Configurations for any Vault. - Proficiency in implementing, supporting, and administering the Veeva Vault platform, including suites such as CTMS, QMS, Safety, and eTMF. - Defining and implementing global business processes for safety, demonstrating the ability to navigate international regulations and associated business processes. - Conducting tech impact assessments on current features and functionalities in response to n...

As a Senior / Principal Stat Programmer at Syneos Health, you will play a crucial role in accelerating customer success by applying your expertise in SAS/ R and SQL programming. Your contributions will directly impact the development of novel FDA approved drugs and EMA authorized products, shaping the future of drug development processes globally. **Key Responsibilities:** - Utilize your 5+ years of experience in Advanced SAS/ R programming and SQL to develop programs and provide statistical programming support for statisticians or for client/business use. - Demonstrate proficiency in R programming, R Package development, and a strong knowledge of SQL. - Enhance your skills by leveraging han...

The position is based in Hyderabad and you must be available for a face-to-face interview for the second round. Your primary responsibilities will include collaborating with business stakeholders to streamline end-to-end clinical operations processes and translating business requirements into technical specifications for development teams. You will define and communicate the product feature vision, ensuring alignment with business objectives and collaborating with stakeholders to design, implement, and manage Clinical Operations solutions. As part of the role, you will create a strategic roadmap for Veeva Vault Clinical Operations applications, oversee the software development lifecycle, and...

We are looking for a detail-oriented and motivated Product Manager to join our team. As a Product Manager, you will be the subject matter expert for our healthcare products and solutions, collaborating closely with development and support teams to deliver high-quality solutions. Your responsibilities will include supporting strategic product planning, development lifecycle, and product launch cycles for our product offerings. You will drive the execution of processes in the product lifecycle, such as product and market research, competitor analysis, planning, positioning, requirements and roadmap development, and product launch. Additionally, you will collaborate with stakeholders to define,...

As a Veeva Config Specialist, you will leverage your 5-8 years of experience in the life sciences sector, with a strong focus on Veeva Vault Configurations. Your expertise will be crucial in implementing, supporting, and administering the Veeva Vault platform across various suites such as CTMS, QMS, Safety, eTMF, and more. Your primary responsibilities will include defining and implementing global business processes for safety, ensuring compliance with international regulations, and conducting tech impact assessments on current features and functionalities to accommodate new releases and enhancements. You will play a key role in guiding business decisions and priorities by proposing effectiv...

- UG/PG in Statistics, Mathematics, Life sciences, Engineering or Computer related subjects - Min. 6 yrs Exp in Statistical Programming-TLF,ADAM,SDTM,SAS Macros Developement CALL@WHATSAPP- RUKHSAR-9899875055 SHRUTI- 9911988551 SUHANI-9911988552