Clinical Programmer Ii

1 day ago


Bengaluru, India Syneos Health Clinical Full time

**Description**

**Clinical Programmer II**

Come discover what our 25,000+ employees already know: work here matters everywhere. We’re a growing and evolving biopharmaceutical industry leader, which means you’ll have endless opportunities to work with experts around the world and build the career you’ve dreamed of.
As a part of the Syneos Health team, you’ll help us deliver results for a rewarding reason - we improve patients’ lives around the world. Because to us, a patient isn’t just a number, they’re our family, friends, and neighbors.

**Why Syneos Health**
- #SyneosHealthLife means we’re committed to our Total Self culture - where everyone can authentically be themselves. Our Total Self culture is what unites us globally, and we know every person’s unique contributions make a difference.
- We believe our success is a direct result of the people who are driving it - you We value your dedication to care for our customers and patients, so we want to focus on taking care of you. That’s why we offer a comprehensive benefits program encompassing your total health - physical, mental and financial.
- 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**
- Utilizes primary development tools including Oracle RDC, Oracle Inform, Medidata, Rave, SAS, and other supporting tools to design, write, validate, and maintain software to meet specifications in a timely and productive manner following standard development procedures.
- Generates and maintains all required documentation, including the development of specifications, coding, and validation efforts in support of annotated Case Report Forms (CRFs), database creation, coding configuration, edit check procedures, import setup and processing, export setup and processing, listings, and custom reports.
- Serves on project teams to coordinate and lead development activities for clinical programming projects. Attends meetings, participates in discussions, uses an analytical approach to problem solving, focuses on deliverables, and provides constructive feedback. Keeps those responsible for project management informed of any issues that might impact project target dates, scope, or budget and escalates potential problems effectively and in a timely manner. Balances multiple task assignments and communicates needs to supervisor to obtain needed resources.
- Ensures quality deliverables by providing review of study level core deliveries for accuracy. Attends sponsor audits and assists with in-progress audits.
- Reviews and provide input on study budgets and monitors scope of work to actual work, alerting management of potential change orders.
- Provides leadership, training, guidance, and support to other department members based upon expertise in specific skill sets. Collaborates with clients, peers, lead programmers, project teams and/or requestors to clarify and finalize specifications, and uses expanded technical skills to meet evolving project needs.
- Assists in project review meetings and assists with departmental review meetings.
- Attends Quick Start Camps (QSCs) as the lead clinical programmer for assigned studies.
- Leads clinical programming activities on up to eight (8) concurrent studies depending upon scope, similarity, program, and resourcing requirements.
- Manages project resources, proactively alerting management of delivery and resourcing needs.
- Possesses and maintains a broad overall knowledge in the field of clinical programming and clinical data management by reading related literature, self-training, attending training classes, attending professional meetings, etc.

**Qualifications**

**What we’re looking for**
- Bachelor’s degree preferred, In lieu of Bachelor’s degree, equivalent related education and experience.
- The ability to deal effectively with sponsors and internal customers at all levels.
- Excellent communication and interpersonal skills, both written and spoken, with an ability to inform.
- Demonstrated experience in managing multiple priorities in a highly dynamic environment
- Experience working in a matrix-structured environment is preferred
- Experience with programming languages, such as PL/SQL, SAS, C#, or VB preferred.
- Ability to travel as necessary (up to 25%)

**Get to know Syneos Health**
We are the only full-service biopharmaceutical solutions company in the world. That means we bring together the best clinical and commercial minds to create a better, smarter, faster way to get medicines into the hands of patients who need it most. Learn more about Syneos Health.

**Additional Information**:
Tasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company, at its sole discretion and with no prior notice, may assign o



  • Bengaluru, Karnataka, India AstraZeneca Full time

    **Job Title: Clinical Programmer II** **Career Level - C** **Introduction to role** Are you ready to be part of a team that turns drug development strategies into reality? As a Clinical Programmer II, you will support programming, dashboard development, and validation of data cleaning and review listings for ongoing clinical studies with medium to high...


  • Bengaluru, India Novotech Asia Full time

    **Brief Position Description**: The Clinical Data Programmer SAS is responsible for data analysis and business intelligence activities related to study related clinical and operational data for the purpose of facilitating clinical data inspection and quality control, as well as operational performance control of clinical sites by creating reports,...


  • Bengaluru, India Bayer Full time

    **At Bayer we’re visionaries, driven to solve the world’s toughest challenges and striving for a world where ,Health for all, Hunger for none’ is no longer a dream, but a real possibility. We’re doing it with energy, curiosity and sheer dedication, always learning from unique perspectives of those around us, expanding our thinking, growing our...


  • Bengaluru, Karnataka, India George Clinical Full time

    Company Overview:Established in Asia-Pacific, our organization is a leading global clinical research organization driven by scientific expertise and operational excellence. With over 20 years of experience and 500+ people managing 39+ geographical locations throughout the Asia-Pacific region, USA, and Europe, we offer a full range of clinical trial services...


  • Bengaluru, Karnataka, India AstraZeneca Full time

    **Job Title: Clinical Programmer I** **Career Level - C** **Introduction to role** Are you passionate about programming and clinical trials? As a Clinical Programmer I, you will support programming and validation activities for data cleaning and review listings in ongoing clinical studies. Working under the guidance of an experienced programmer, you will...


  • Bengaluru, Karnataka, India George Clinical Full time

    We are a leading global clinical research organization, founded in the Asia-Pacific region and driven by scientific expertise and operational excellence. With over 20 years of experience and a team of 500+ people managing 39+ geographical locations throughout the Asia-Pacific region, USA, and Europe, we offer a full range of clinical trial services to...


  • Bengaluru, India Quanticate Full time

    **Overview**: An exciting opportunity for a SAS Programmer has arisen within our Clinical Research Organisation (CRO), Quanticate. Working from our Bangalore/Hyderabad, India office, you will work within Quanticate’s global programming department, providing the highest quality statistical programming...


  • Bengaluru, India Trigent Software Inc Full time

    Title: Principal Clinical Data Science ProgrammerLocation: Bangalore/Chennai/Trivandrum (Remote/Hybrid)Experience: 6+ YearsAbout Us:We are a leading organization in the clinical research sector, committed to delivering high-quality data solutions. We are seeking a Principal Clinical Data Science Programmer to join our dynamic team and contribute to...

  • SDTM Programmer II

    5 days ago


    Bengaluru Urban, India Excelya Full time

    Excelya, one of the leading independent CRO in Europe.Created in 2014, Excelya is a people-centered Contract Research Organization (CRO) that excels with care.We offer a personal and authentic experience within a young, ambitious health company on the path to becoming the clinical research leader in Europe thanks to our 900 Excelyates. Our unique one-stop...


  • Bengaluru, India Trigent Software Inc Full time

    Title: Principal Clinical Data Science ProgrammerLocation: Bangalore/Chennai/Trivandrum (Remote/Hybrid)Experience: 6+ YearsAbout Us:We are a leading organization in the clinical research sector, committed to delivering high-quality data solutions. We are seeking a Principal Clinical Data Science Programmer to join our dynamic team and contribute to...


  • Bengaluru, India Trigent Software Inc Full time

    Title: Principal Clinical Data Science Programmer Location: Bangalore/Chennai/Trivandrum (Remote/Hybrid) Experience: 6+ Years About Us: We are a leading organization in the clinical research sector, committed to delivering high-quality data solutions. We are seeking a Principal Clinical Data Science Programmer to join our dynamic team and contribute to...


  • Bengaluru, India Trigent Software Inc Full time

    Title: Principal Clinical Data Science ProgrammerLocation: Bangalore/Chennai/Trivandrum (Remote/Hybrid)Experience: 6+ YearsAbout Us:We are a leading organization in the clinical research sector, committed to delivering high-quality data solutions. We are seeking a Principal Clinical Data Science Programmer to join our dynamic team and contribute to...


  • Bengaluru, India Novotech Asia Full time

    **Minimum Qualifications & Experience**: - Graduate in computer science, data science, mathematics, or life science related field, or similar. - A minimum of 2 years of experience in a role related to business intelligence, data science, data analysis, and clinical data management or clinical data programming in a pharmaceutical company, CRO or EDC software...


  • Bengaluru, India Ergomed Full time

    Company Description Ergomed PLC is a rapidly expanding full service mid-sized CRO specialising in Oncology and Rare Disease. Since its foundation in 1997 the company has grown organically and steadily by making strategic investments and landmark acquisitions, with operations in Europe, North America and Asia Our company allows for employee visibility (you...


  • Bengaluru, Karnataka, India Novasyte Full time

    Good Clinical Domain knowledge with understanding of clinical phases and Work experience must be in clinical / healthcare domain. Experience in Clinical SAS Programming Experience in Data Import Programming using SAS, SAS Output Delivery system (ODS) for generating reports in specific output formats like RTF, PDF, and HTML. Handling missing values,...


  • Bengaluru, India Trigent Software Inc Full time

    Title: Principal Clinical Data Science ProgrammerLocation:Bangalore/Chennai/Trivandrum (Remote/Hybrid)Experience:6+ YearsAbout Us:We are a leading organization in the clinical research sector, committed to delivering high-quality data solutions. We are seeking a Principal Clinical Data Science Programmer to join our dynamic team and contribute to innovative...


  • Bengaluru, India ApicalGo Consultancy Full time

    Primary Purpose:We are seeking a talented R Shiny programmer to develop interactive reports that translate clinical trial data into clinical insights. As an R Shiny programmer you will design, develop, deploy, and optimize user-friendly interactive web applications for clinical data analysis and visualization. You will work closely with data scientists,...


  • Bengaluru, Karnataka, India Novo Nordisk Full time

    Associate Clinical Data Programmer **Category**:Data & AI**Location**:Bangalore, Karnataka, IN- ..- We commit to an inclusive recruitment process and equality of opportunity for all our job applicants.- At Novo Nordisk we recognize that it is no longer good enough to aspire to be the best company in the world. We need to aspire to be the best company for...


  • Bengaluru, India Novotech Asia Full time

    Brief Position Description: Supports the day-to-day operations of the data management projects, providing in-house data entry support to projects and administrative support to CDMs, according to GCDMP guidelines, local regulatory requirements, and Novotech/Client SOPs. Minimum Qualifications & Experience: Graduate in a clinical or life sciences related...


  • Bengaluru, Karnataka, India Teva Pharmaceuticals Full time

    About Us">Teva Pharmaceuticals is a leading manufacturer of generic medicines and the proud producer of many products on the World Health Organization's Essential Medicines List.">We're committed to making good health more affordable and accessible to millions around the world, helping people enjoy healthier lives.">The Opportunity">As a Senior Clinical...