Ts Senior clinical data associate Jobs – 57 Open Jobs Today

Senior Clinical Data Associate
Precision Medicine Group —Hyderabad, Telangana
- Online application
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
3d
Junior Associate - Evidence Synthesis, Clinical Outcome assessments (COA)
Sanofi —Hyderabad, Telangana
- Full-time
- Writing skills
- English
- Analysis skills
Senior Associate - Clinical Pharmacology
Amgen —Hyderabad, Telangana
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
1d
Senior Associate, Strategic Planning & Operations
Amgen —Hyderabad, Telangana
- Microsoft Excel
- Microsoft Office
- Master's degree
1d
Senior Global Trial Associate
Bristol-Myers Squibb —Hyderabad, Telangana
- Email
- Hybrid work
- B.Sc
- Project management
- Bachelor's degree
7d
Senior Associate Medical Data Reviewer
Amgen —Hyderabad, Telangana
- Nursing
- Medicine
- Data analysis skills
Senior Associate- Systematic Literature Reviews
Amgen —Hyderabad, Telangana
- Full-time
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Data Management Sr Associate
Amgen —Hyderabad, Telangana
- Bachelor's degree
- In-person
Sr Associate Clinical master data management
Amgen —Hyderabad, Telangana
- Microsoft Powerpoint
- Microsoft Excel
- Oracle
Biostatistical Programming Senior Associate
Amgen —Hyderabad, Telangana
- B.Sc
- Master's degree
- Bachelor's degree
R&D Clinical - Quality Compliance Senior Manager
Amgen —Hyderabad, Telangana
- English
- Master's degree
- Analysis skills
Sr Associate Quality
Amgen —Hyderabad, Telangana
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Global HEOR Economic Modelling Senior Associate
Amgen —Hyderabad, Telangana
- Microsoft Excel
- English
- Master's degree
Senior Associate Clinical Supply Chain – Global Clinical Customer Service (GCCS)
Amgen —Hyderabad, Telangana
- Salesforce
- ERP systems
- Microsoft Office
Biostatistics Sr Associate – Data Visualization
Amgen —Hyderabad, Telangana
- Doctoral degree
- English
- Master's degree
Senior Manager Program Data Delivery
Amgen —Hyderabad, Telangana
- Computer Science
- Research
- Master's degree
Biostatistics Sr Assoc (Study Statistician)
Amgen —Hyderabad, Telangana
- Doctoral degree
- English
- Master's degree
Clinical Supply Chain Senior Associate – Development Supply Chain Technologies (DSCT)
Amgen —Hyderabad, Telangana
- Master's degree
- Bachelor's degree
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Study Delivery Sr Associate
Amgen —Hyderabad, Telangana
- Microsoft Powerpoint
- Microsoft Word
- Research
Senior Manager, Scientific and Operations Intelligence - Obesity
Amgen —Hyderabad, Telangana
- Master's degree
- Analysis skills
- Bachelor's degree

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Senior Clinical Data Associate

Precision Medicine Group -
Hyderabad, Telangana

Apply Now

Job details

3 days ago

Qualifications

Microsoft Powerpoint
Microsoft Word
Microsoft Excel
Microsoft Outlook
Clinical research
Software troubleshooting
SAP
Medical coding
English
Microsoft Office
Bachelor's degree
Data management
Data entry
Communication skills

Full job description

Position Summary:

The Senior Clinical Data Associate provides data management support and assistance in all aspects of the clinical trial data management process from study start up to post database lock for assigned projects under direct supervision. Standard Operating Procedures / Work Instructions (SOPs/WIs); regulatory directives; study specific plans and guidelines will be followed. This position may perform database development and testing, as well as additional data management activities.

Essential functions of the job include but are not limited to:

Support the Lead DM as a back-up and/or team member, ensuring continuity, responsiveness, and that tasks are performed in a timely manner
May perform data entry for paper-CRF studies, as needed
May perform quality control of data entry
May provide input into timelines. Ensure that clinical data management deadlines are met with quality. May assess resource needs for assigned projects, as needed.
Assist in developing CRF specifications from the clinical study protocol and coordinate the review/feedback from all stakeholders
May assist in building clinical databases
Conduct database build UAT and maintain quality controlled database build documentation. May oversee overall quality of the clinical database.
Assist in specifying requirements for all edit check types e.g., electronic, manual data review, edit checks, etc.
Responsible for creating, revising, appropriate versioning and maintaining data management documentation.
Train clinical research personnel on the study specific CRF, EDC, and other project related items as needed.
Review and query clinical trial data according to the Data Management Plan
Perform line listing data review based on the guidance provided by the sponsor and/or Lead DM
Run patient and study level status and metric reporting
Perform medical coding of medical terms relative to each other in order to ensure medical logic and consistency
Assist with coordinating SAE/AE reconciliation
Assist with liaising with third-party vendors such as external data and EDC vendors in a project-manager capacity in support of timelines and data-related deliverables
May assist with SAS programming and quality control of SAS programs used in the Data Management department
Identify and troubleshoot operational problems, issues, obstacles, and barriers for studies based on metrics data, audit reports, and input from project team members and other stakeholders
May assist in reviewing and providing feedback on protocols, Statistical Analysis Plans (SAP) and Clinical Study Reports (CSRs), if required by the project
May assist in participating in the development and maintenance of Standard Operating Procedures (SOPs) and corresponding process documentation related to data management and database management activities
Trains and ensures that all data management project team members have been sufficiently trained
Communicate with study sponsors, vendors and project teams as needed regarding data, database or other relevant project issues
May present software demonstrations/trainings, department/company training sessions, present at project meetings
May require some travel
Perform other duties as assigned.

Qualifications:

Minimum Required:

5+ years' experience
Bachelors and/or a combination of related experience

Other Required:

Proficiency in Microsoft Office: Word, Excel, PowerPoint, Outlook.
Able to handle a variety of clinical research tasks.
Excellent organizational and communication skills
Professional use of the English language; both written and oral.
Basic knowledge of drug, device and/or biologic development and effective data management practices.

Preferred:

Experience in a clinical, scientific or healthcare discipline.
Dictionary medical coding (MedDRA and WHODrug)
Understanding of CDISC standards (CDASH, SDTM, ADaM, etc.…)
Oncology and/or Orphan Drug therapeutic experience

Skills:

Demonstrates strong knowledge of ICH-GCP, relevant Precision Oncology SOPs, and regulatory guidance, as well as the ability to implement and drive outcomes

Competencies:

Motivates project team members to meet timelines and project goals
Focuses on continuous improvement, including the ability to make proactive assessments on how to make processes more efficient and people more effective
Resolves project related problems and prioritizes workload to meet deadlines with minimal support
Exhibits a high degree of self-motivation, and can work and plan independently as well as in a team environment
Demonstrates an acceptable degree of professionalism, as evidenced by punctuality, ability to deliver on commitments, an understanding of the service culture and positive interactions with customers and teammates, including good interpersonal skills

Any data provided as a part of this application will be stored in accordance with our Privacy Policy. For CA applicants, please also refer to our CA Privacy Notice.

Precision Medicine Group is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, age, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status or other characteristics protected by law.

If you are an individual with a disability and require a reasonable accommodation to complete any part of the application process or are limited in the ability or unable to access or use this online application process and need an alternative method for applying, you may contact Precision Medicine Group at [email protected].

Recruitment Fraud Warning: Please be aware that fraudulent individuals and websites may impersonate Precision Medicine Group or its affiliates and attempt to obtain personal, financial, or banking information through fake job postings or employment offers. Precision Medicine Group will never request payment, banking details, or other sensitive financial information as part of the recruitment process. If you believe you have been targeted by a recruitment scam, we encourage you to report the incident to your local law enforcement authorities, consumer protection agency, or relevant cybercrime reporting organization in your country. Please also notify us at [email protected] so we can investigate and take appropriate action.

Apply Now

Refine Your Search

senior clinical data associate jobs in ts

Senior Clinical Data Associate

Junior Associate - Evidence Synthesis, Clinical Outcome assessments (COA)

Senior Associate - Clinical Pharmacology

Senior Associate, Strategic Planning & Operations

Senior Global Trial Associate

Senior Associate Medical Data Reviewer

Senior Associate- Systematic Literature Reviews

Data Management Sr Associate

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Biostatistical Programming Senior Associate

R&D Clinical - Quality Compliance Senior Manager

Sr Associate Quality

Global HEOR Economic Modelling Senior Associate

Senior Associate Clinical Supply Chain – Global Clinical Customer Service (GCCS)

Biostatistics Sr Associate – Data Visualization

Senior Manager Program Data Delivery

Biostatistics Sr Assoc (Study Statistician)

Clinical Supply Chain Senior Associate – Development Supply Chain Technologies (DSCT)

Study Delivery Sr Associate

Senior Manager, Scientific and Operations Intelligence - Obesity

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