Kukatpally Hyderabad Telangana General medicine Jobs – 119 Open Jobs Today

Manager, CSAR – Custom function Programming
Amgen —Hyderabad, Telangana
- Computer Science
- Project management
- Bachelor's degree
Senior Medical Regulatory Writer
Sanofi —Hyderabad, Telangana
- Full-time
- Medicine
- Doctoral degree
- Writing skills
Senior Manager, Process Intelligence - Results Delivery Office
Amgen —Hyderabad, Telangana
- Master's degree
- SQL
- Project management
Job Posting Title Senior Associate, Incentive Compensation Inquiry & Data Operations
Amgen —Hyderabad, Telangana
- Microsoft Excel
- Master's degree
- SQL
Senior Associate BC Engineer - AI & Automation
Amgen —Hyderabad, Telangana
- Master's degree
- Analysis skills
- Project management
Neural Nexus – Data Steward, Data & AI Enablement (AuRA)
Amgen —Hyderabad, Telangana
- Project management
- Agile
- In-person
Manager Compensation Related Benefits
Amgen —Hyderabad, Telangana
- Master's degree
- Project management
- In-person
Registrar
Basavatarakam Indo American Cancer Hospital & Research Institute —Hyderabad, Telangana
- Full-time
- Medicine
Interventional Cardiologist
MY HEALTH HOSPITAL —KPHB Colony, Hyderabad, Telangana
- ₹4,00,000 - ₹4,20,000 a month
- Full-time
- Medicine
- Bachelor's degree
- In-person
Quick apply
Sr Associate IS Analyst - Veeva Vault Release Engineer
Amgen —Hyderabad, Telangana
- Night shift
- Computer Science
- Public speaking
- Master's degree
Sr Associate IS Analyst – Veeva Automation Engineer
Amgen —Hyderabad, Telangana
- Computer science
- DevOps
- Public speaking
Senior Associate DR Engineer - AI & Automation
Amgen —Hyderabad, Telangana
- Master's degree
- Analysis skills
- Project management

More jobs to discover

Find similar jobs that you might be interested in.

Senior Regulatory Medical Writer
Jeevan —Hyderabad, Telangana
A relevant advanced degree (e.g. MS Pharmacy, PharmD, PhD, MD) is preferred, and higher education may compensate for years of experience.
Senior Medical Regulatory Writer
Sanofi —Hyderabad, Telangana
Experience: >5 years of experience in regulatory writing for the pharmaceuticals/healthcare industry, pharmacovigilance, clinical drug development, or closely…

I want to receive the latest job alerts for general medicine in kukatpally hyderabad telangana

By signing in to your account, you agree to SimplyHired's Terms of Service and consent to our Cookie and Privacy Policy.

Explore jobs in more locations

general medicine jobs near kukatpally hyderabad telangana

Registrar jobs in Hyderabad, Telangana

Release Engineer jobs in Hyderabad, Telangana

Senior Operations Associate jobs in Hyderabad, Telangana

Event Manager jobs in Hyderabad, Telangana

Senior Automation Engineer jobs in Hyderabad, Telangana

Medical Writer jobs in Hyderabad, Telangana

Registrar jobs in Himayatnagar, Hyderabad, Telangana

Assistant Registrar jobs in Kolkata, West Bengal

Vacancy Registrar jobs in Pune, Maharashtra

Required Registrar jobs in Mumbai, Maharashtra

University Assistant Registrar jobs in Anywhere

Junior Registrar jobs in Maharashtra

Senior Associate Engineer jobs in Shivaji Park, Mumbai, Maharashtra

Senior Associate Engineer jobs in Silvassa, Daman And Diu

Senior Associate Engineer jobs in Solan, Himachal Pradesh

Graduate Engineer Trainee jobs in Bengaluru, Karnataka

Fresher Data Engineer jobs in Bengaluru, Karnataka

Senior Associate Engineer jobs in Lucknow, Uttar Pradesh

Graduate Engineer Trainee jobs in Maharashtra

Biomedical Engineer, Internship jobs in Bengaluru, Karnataka

Manager, CSAR – Custom function Programming

Amgen -
Hyderabad, Telangana

Apply Now

Job details

Qualifications

Clinical research
Computer Science
Performance management
Database management
Project management
Bachelor's degree
Data management
Clinical trials
Business Administration
SDLC

Full job description

India - Hyderabad

JOB ID: R-214615 LOCATION: India - Hyderabad WORK LOCATION TYPE: On Site DATE POSTED: May. 02, 2025 CATEGORY: Information Systems

Join Amgen’s Mission of Serving Patients

At Amgen, if you feel like you’re part of something bigger, it’s because you are. Our shared mission—to serve patients living with serious illnesses—drives all that we do.

Since 1980, we’ve helped pioneer the world of biotech in our fight against the world’s toughest diseases. With our focus on four therapeutic areas –Oncology, Inflammation, General Medicine, and Rare Disease– we reach millions of patients each year. As a member of the Amgen team, you’ll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives.

Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lay within them, you’ll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career.

Job Description

We are looking for a talented individual to join us as a Study Designer and Edit Check Programmer, reporting directly to the Sr. Manager, Clinical Systems and Analytical Reporting.

The successful candidate will play a crucial role in adhering to Amgen standards, procedures, and best practices to build and program studies in our clinical trial database. This position will require effective partnership with other CSAR Operations and cross-functional staff to ensure seamless, high-quality deliverables and activities related to the use of electronic data capture technology.

We are seeking a strong leader who can confidently influence stakeholders and contribute individually to study-specific and general CSAR/GDO projects or operational work. The ideal candidate will have proven experience in partnering effectively with cross-functional teams to deliver systems support and study deliverables. Additionally, they should have operational experience with clinical database management systems and allied technologies (e.g., Rave EDC, Veeva EDC).

Responsibilities include, but are not limited to, the following:

Support of clinical trial platform technologies
Support decision-making by acting as a data scientist bringing awareness to patterns and analytical insight.
Coordinating and providing programming support to Clinical Study Teams
Ensure efficient and consistent use of EDC system and ensure the use is complied with the established procedures or standards.
Acting as a technical point of contact for systems deliverables on defined programs
Identify, recommend or implement system enhancements, new tools or emerging technologies to decrease database development cycle times and foster a collaborative working environment.
Providing technical and business process input / expertise on new and emerging technologies
Develop, review and implement policies, SOPs and associated documents
Ensure documentation supports CSAR operational or technical activities is in a complete manner and consistent with regulatory and the established processes.
Assist in preparing for and responding to audit findings (internal or external).

Knowledge

Good Clinical Practice
Strong understanding and experience in the use of performance management techniques, measures, problem-solving and analytical thinking
Drug development and clinical trials processes
Data management processes
Clinical trial databases and applications
Edit check development and Custom function programing
Programming Languages
Systems development lifecycle
Project planning and management
Collaborating with global cross-functional teams (team/matrix environment)
Quality management and Risk Analysis
Regulatory filings and inspections
Process improvement methodologies

Preferred Qualifications

Advanced degree or equivalent in life science, computer science, math, statistics, business administration or related discipline
Broad knowledge / work experience in data management / programming in the Pharmaceutical or Biotech arena
General project management and planning experience
Experience in oversight of outside vendors (CRO’s, central labs, imaging vendors, IRT vendors, etc.)

Basic Qualifications

Bachelors degree or equivalent in life science, computer science, business administration or related discipline with 9 to 12 years of experience
Specialist knowledge / experience in life sciences or a medically related field
General biopharmaceutical clinical research experience (clinical research experience obtained working on clinical trials at a biotech, pharmaceutical or CRO company)

Apply Now

Refine Your Search

general medicine jobs in kukatpally hyderabad telangana

Manager, CSAR – Custom function Programming

Senior Medical Regulatory Writer

Senior Manager, Process Intelligence - Results Delivery Office

Job Posting Title Senior Associate, Incentive Compensation Inquiry & Data Operations

Senior Associate BC Engineer - AI & Automation

Neural Nexus – Data Steward, Data & AI Enablement (AuRA)

Manager Compensation Related Benefits

Registrar

Interventional Cardiologist

Sr Associate IS Analyst - Veeva Vault Release Engineer

Sr Associate IS Analyst – Veeva Automation Engineer

Senior Associate DR Engineer - AI & Automation

More jobs to discover

I want to receive the latest job alerts for general medicine in kukatpally hyderabad telangana

Explore jobs in more locations

Jobseeker tools

Employer Tools

Browse

Stay Connected