Morning - US time zone 8 hours/day - preferably East Coast Temp to Perm: Not at this time Core ... guideline and Teva standards and leads the cross functional review and approval process.
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Morning - US time zone 8 hours/day - preferably East Coast Temp to Perm: Not at this time Core ... guideline and Teva standards and leads the cross functional review and approval process.
Deviation Investigations Specialist
Davie, FL · On-site
$33 - $35/hr
... Temp to perm: Yes based on performance and openings Shift Schedule: Monday - Friday, 8A - 5P ... Teva and require frequent cross-functional collaboration. The individual should be confident in ...
Quick apply
Deviation Investigations Specialist
Davie, FL · On-site
$33 - $35/hr
... Temp to perm: Yes based on performance and openings Shift Schedule: Monday - Friday, 8A - 5P ... Teva and require frequent cross-functional collaboration. The individual should be confident in ...
Temporary Teva information
See salary details
$10.82 - $12.15
2% of jobs
$12.15 - $13.48
2% of jobs
$13.48 - $14.82
12% of jobs
$15.31 is the 25th percentile. Wages below this are outliers.
$14.82 - $16.15
24% of jobs
The median wage is $17.01 / hr.
$16.15 - $17.48
15% of jobs
$17.48 - $18.82
15% of jobs
$19.48 is the 75th percentile. Wages above this are outliers.
$18.82 - $20.15
10% of jobs
$20.15 - $21.48
6% of jobs
$21.48 - $22.81
7% of jobs
$22.81 - $24.15
4% of jobs
$24.15 - $25.48
2% of jobs
$10
$18
$25
How much do temporary teva jobs pay per hour?
As of Aug 14, 2026, the average hourly pay for temporary teva in the United States is $18.38, according to ZipRecruiter salary data. Most workers in this role earn between $15.38 and $19.95 per hour, depending on experience, location, and employer.
What is the difference between Temporary Teva vs Temporary Pharmacist?
| Aspect | Temporary Teva | Temporary Pharmacist |
|---|---|---|
| Credentials | Pharmacy license, relevant certifications | Pharmacy license, certifications |
| Work Environment | Pharmaceutical manufacturing, research labs | Retail pharmacies, hospitals |
| Employer & Industry | Teva Pharmaceuticals, pharmaceutical industry | Various pharmacies, healthcare providers |
Temporary Teva roles typically involve pharmaceutical manufacturing or research, requiring specific industry certifications. Temporary Pharmacist positions are more customer-facing, working in retail or hospital settings. Both roles require pharmacy licensure but differ mainly in work environment and employer focus.
Is a Temporary Teva hiring for entry level positions?
Temporary Teva positions often include entry-level roles suitable for individuals with minimal experience. These jobs typically require basic skills, may involve training, and are available in various departments such as manufacturing, logistics, or administrative support.
What are the most commonly searched types of Teva jobs?
The most popular types of Teva jobs are:
What job categories do people searching Temporary Teva jobs look for?
The top searched job categories for Temporary Teva jobs are:
Contractor
Re-posted yesterday
Job description
Position Details:
Our client, a world-leading Pharmaceutical Company in West Chester, PA is currently looking for an Clinical Data Manager to join their expanding team.
Job Title: Clinical Data Manager (SDTMIG, Pinnacle 21) / REMOTE WORK
Duration: 11 months contract, extendable up to 24 months
Location: West Chester, PA
Our client, a world-leading Pharmaceutical Company in West Chester, PA is currently looking for an Clinical Data Manager to join their expanding team.
Job Title: Clinical Data Manager (SDTMIG, Pinnacle 21) / REMOTE WORK
Duration: 11 months contract, extendable up to 24 months
Location: West Chester, PA
Fully remote position
Note:
The client has the right-to-hire you as a permanent employee at any time during or after the end of the contract.
You may participate in the company group medical insurance plan
Job Description:
Note:
The client has the right-to-hire you as a permanent employee at any time during or after the end of the contract.
You may participate in the company group medical insurance plan
Job Description:
Fully remote position - US Based Candidate.
Title: Clinical Programmer 2 - Manager Level (SDTM)
Shift Schedule:
Title: Clinical Programmer 2 - Manager Level (SDTM)
Shift Schedule:
Morning - US time zone 8 hours/day – preferably East Coast
Temp to Perm:
Temp to Perm:
Not at this time
Core essential:
1. Minimal Bachelor’s degree in any field
2. Minimal 5 years experience with Clinical data, SDTM IG, and Pinnacle 21.
Position Summary:
The Clinical Programming Manager is responsible for managing the timely and accurate execution of programming components of clinical trials.
The Manager leads and manages completed projects that involve global tasks, cross functional teams, or outsourcing resources.
Core essential:
1. Minimal Bachelor’s degree in any field
2. Minimal 5 years experience with Clinical data, SDTM IG, and Pinnacle 21.
Position Summary:
The Clinical Programming Manager is responsible for managing the timely and accurate execution of programming components of clinical trials.
The Manager leads and manages completed projects that involve global tasks, cross functional teams, or outsourcing resources.
The role may require providing input to design and analysis, and report the results of clinical trials, including programming rules and mocked T/L/G.
In addition, providing all safety claims for new drugs and extension of claims/publication support for our marketed drugs.
Major duties and responsibilities:
Responsible to define case report forms (CRFs) specifications in accordance with SDTM guideline and Teva standards and leads the cross functional review and approval process.
Responsible to define external (non CRF) data specifications in accordance with Biometrics standards
Responsible to define data flow and to ensure that study databases meet Teva requirements by performing User Acceptance Testing (UAT)
Responsible to perform, supervise and manage day-to-day activities associated with receipt of clinical (CRF and non CRF) and operational (when relevant) data in accordance with study timelines
Responsible to perform data handling activities on an ongoing basis to ensure accuracy, reliability, integrity, consistency and completeness of the data prior to database lock and providing the final data to clinical programming and statistics after database lock.
Responsible to program SAS or SQL based clinical and operational listings and reports
Responsible to follow Clinical Programming processes and perform programming activities related to clinical, external and operational data receipt and reporting to ensure the data meets Teva requirements and is reported with highest quality to all stakeholders
Develop positive partnerships with CROs and ensure a high standard of deliverables is maintained
Has a good understanding of SAS macros, programs, reporting tools, infrastructure and has programming skills to develop new features, programs and macros
Serves as the focal point on assigned studies for all local interfaces and preserves a fluent workflow with the other interfacing departments and local procedures and processes.
Supports collaboration, communication, coordination and prioritization within the department working in conjunction with Data Management Lead.
Thorough understanding of Clinical data, SDTM IG and Pinnacle 21
Education and Knowledge Requirements:
Bachelor’s or higher degree in science or technology or equivalent combination of education and related work experience
5+ years for Sr Programming Lead professional experience.
Strong and effective oral and written communication skills and interpersonal skills
Ability to manage multiple projects independently
Ability to work in a virtual, global and multi-cultural environment High level of SAS software knowledge
Vast knowledge of CDISC standards
Detail oriented
Major duties and responsibilities:
Responsible to define case report forms (CRFs) specifications in accordance with SDTM guideline and Teva standards and leads the cross functional review and approval process.
Responsible to define external (non CRF) data specifications in accordance with Biometrics standards
Responsible to define data flow and to ensure that study databases meet Teva requirements by performing User Acceptance Testing (UAT)
Responsible to perform, supervise and manage day-to-day activities associated with receipt of clinical (CRF and non CRF) and operational (when relevant) data in accordance with study timelines
Responsible to perform data handling activities on an ongoing basis to ensure accuracy, reliability, integrity, consistency and completeness of the data prior to database lock and providing the final data to clinical programming and statistics after database lock.
Responsible to program SAS or SQL based clinical and operational listings and reports
Responsible to follow Clinical Programming processes and perform programming activities related to clinical, external and operational data receipt and reporting to ensure the data meets Teva requirements and is reported with highest quality to all stakeholders
Develop positive partnerships with CROs and ensure a high standard of deliverables is maintained
Has a good understanding of SAS macros, programs, reporting tools, infrastructure and has programming skills to develop new features, programs and macros
Serves as the focal point on assigned studies for all local interfaces and preserves a fluent workflow with the other interfacing departments and local procedures and processes.
Supports collaboration, communication, coordination and prioritization within the department working in conjunction with Data Management Lead.
Thorough understanding of Clinical data, SDTM IG and Pinnacle 21
Education and Knowledge Requirements:
Bachelor’s or higher degree in science or technology or equivalent combination of education and related work experience
5+ years for Sr Programming Lead professional experience.
Strong and effective oral and written communication skills and interpersonal skills
Ability to manage multiple projects independently
Ability to work in a virtual, global and multi-cultural environment High level of SAS software knowledge
Vast knowledge of CDISC standards
Detail oriented