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 ...
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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 ...
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Inventory Data Analyst (SAP, Power BI, Excel) Duration: 9 months contract, extendable up to 24 Months Location: Memphis, TN Note: The client has the right-to-hire you as a permanent employee at any ...
You will collect and organize data, prepare reports, and ensure inspection readiness while addressing routine quality inquiries. Key Responsibilities Collaborate with cross-functional teams to ...
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You will collect and organize data, prepare reports, and ensure inspection readiness while addressing routine quality inquiries. Key Responsibilities Collaborate with cross-functional teams to ...
The main function of a Pharmacology Associate is to support drug development and research by conducting laboratory experiments, analyzing pharmacological data, and assisting in the evaluation of drug ...
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The main function of a Pharmacology Associate is to support drug development and research by conducting laboratory experiments, analyzing pharmacological data, and assisting in the evaluation of drug ...
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Biostatistician
Raritan, NJ · On-site
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This role involves hands-on work with analytical and characterisation techniques, contributing directly to data generation, method optimisation, and problem-solving. Bench Scientists differ from lab ...
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Tampa, FL · On-site
$19.75 - $26/hr
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HR Coordinator (Workday, ADP) / Hybrid Work
Tampa, FL · On-site
$19.75 - $26/hr
Ensure data integrity for all HR systems and databases within the required Compliance framework. Synthesize various reports using MS Excel or similar. Provide administrative support as needed (e.g ...
This role plays a critical part in ensuring the integrity, accuracy, and compliance of pathology data used to support candidate selection, first-in-human studies, early research, target safety ...
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This role plays a critical part in ensuring the integrity, accuracy, and compliance of pathology data used to support candidate selection, first-in-human studies, early research, target safety ...
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Andover, MA · On-site
$35.75 - $44.75/hr
Strong data organization and analysis skills. Strong communication skills. Additional Information All your information will be kept confidential according to EEO guidelines.
Bench Scientist
Andover, MA · On-site
$35.75 - $44.75/hr
Strong data organization and analysis skills. Strong communication skills. Additional Information All your information will be kept confidential according to EEO guidelines.
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Parsippany, NJ · On-site
You may participate in the company group medical insurance plan Safety Data Management Specialist Reports to Country Safety Lead or Safety Team Lead or Safety Officer Review, preparation, and ...
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Drug Safety Associate
Parsippany, NJ · On-site
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Lab Technician I
Groton, CT · On-site
$19 - $25/hr
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Lab Technician I
Groton, CT · On-site
$19 - $25/hr
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Bioanalytical Scientist / Molecular Assessment
Cambridge, MA · On-site
$38.50 - $48.25/hr
Analyze and interpret experimental data to support selection of lead biotherapeutic molecules. Contribute to improvement activities aimed at increasing efficiency and throughput within the group.
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Bioanalytical Scientist / Molecular Assessment
Cambridge, MA · On-site
$38.50 - $48.25/hr
Analyze and interpret experimental data to support selection of lead biotherapeutic molecules. Contribute to improvement activities aimed at increasing efficiency and throughput within the group.
Document experiments, analyze data, and provide reporting using an electronic laboratory notebook in accordance with Client/GCLP requirements. With guidance, the individual will execute assay routine ...
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Document experiments, analyze data, and provide reporting using an electronic laboratory notebook in accordance with Client/GCLP requirements. With guidance, the individual will execute assay routine ...
Medical Writer / ABPI Code (Association of the British Pharmaceutical Industry)
Cambridge, MA · On-site
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Medical Writer / ABPI Code (Association of the British Pharmaceutical Industry)
Cambridge, MA · On-site
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Organize and reconcile data from disparate sources in formats that are suitable for data analysis presentable to regulatory authorities. Analyze historical manufacturing, product stability and ...
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... data, analyze data, research markets, identify opportunities and risks and understand dependencies before proposing and implementing recommendations for quick wins and value creation 5% ...
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Quality Analyst (Warehouse Management, Temperature control) / Pharma Industry
Shepherdsville, KY · On-site
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Serving as a clinical team member assigned to data review for clinicians, including: Verification of subject eligibility based on medical history Critical application of protocol-defined study ...
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Contractor
Posted 27 days ago
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