Our client, a world leader in diagnostics and life sciences, is looking for a “Clinical Science Program Specialist (100% Remote)". Job Duration: Long Term Contract (Possibility Of Extension)Pay Rate : $35/hr on W2 Company Benefits: Medical, Dental, Vision, Paid Sick leave, 401K Coordinate and manage multiple clinical testing and laboratory services projects from initiation through completion, serving as the primary point of contact for pharmaceutical clients. Drive cross-functional project execution, oversee sample workflow activities, and ensure timely, accurate delivery of clinical study results in a regulated environment. Key Responsibilities:Manage multiple clinical testing and lab services projects under the guidance of the Program Manager.Develop project plans, timelines, and coordinate cross-functional activities to ensure on-time execution.Monitor project progress, identify risks and bottlenecks, and implement solutions to maintain milestones.Oversee sample processing workflows and ensure accurate reporting of results.Serve as the primary liaison for pharmaceutical clients, CROs, site investigators, and internal stakeholders.Coordinate meetings, prepare agendas, document minutes, and communicate project updates.Track and maintain project reports and clinical study data.Promote best practices and continuous improvement across clinical operations. Qualifications:Bachelor’s degree required; Life Sciences preferred.2+ years of project coordination, clinical trial coordination, or project management experience in the CRO, diagnostics, pharmaceutical, or regulated industry.Exposure to clinical studies and regulated documentation.Strong organizational, communication, and collaboration skills.Ability to manage multiple projects in a fast-paced environment. Preferred Qualifications:Experience with companion diagnostics (CDx), clinical testing, or biosample management.Knowledge of clinical trial management processes and PMI methodologies.Experience within the diagnostics or pharmaceutical industry. If interested, please send us your updated resume [email protected]/[email protected] client, a world leader in diagnostics and life sciences, is looking for a “Clinical Science Program Specialist (100% Remote)". Job Duration: Long Term Contract (Possibility Of Extension)Pay Rate : $35/hr on W2 Company Benefits: Medical, Dental, Vision, Paid Sick leave, 401K Coordinate and manage multiple clinical testing and laboratory services projects from initiation through completion, serving as the primary point of contact for pharmaceutical clients. Drive cross-functional project execution, oversee sample workflow activities, and ensure timely, accurate delivery of clinical study results in a regulated environment. Key Responsibilities:Manage multiple clinical testing and lab services projects under the guidance of the Program Manager.Develop project plans, timelines, and coordinate cross-functional activities to ensure on-time execution.Monitor project progress, identify risks and bottlenecks, and implement solutions to maintain milestones.Oversee sample processing workflows and ensure accurate reporting of results.Serve as the primary liaison for pharmaceutical clients, CROs, site investigators, and internal stakeholders.Coordinate meetings, prepare agendas, document minutes, and communicate project updates.Track and maintain project reports and clinical study data.Promote best practices and continuous improvement across clinical operations. Qualifications:Bachelor’s degree required; Life Sciences preferred.2+ years of project coordination, clinical trial coordination, or project management experience in the CRO, diagnostics, pharmaceutical, or regulated industry.Exposure to clinical studies and regulated documentation.Strong organizational, communication, and collaboration skills.Ability to manage multiple projects in a fast-paced environment. Preferred Qualifications:Experience with companion diagnostics (CDx), clinical testing, or biosample management.Knowledge of clinical trial management processes and PMI methodologies.Experience within the diagnostics or pharmaceutical industry. If interested, please send us your updated resume [email protected]/[email protected]

Our client, a world leader in diagnostics and life sciences, is looking for a “Clinical Science Program Specialist (100% Remote)".

Our client, a world leader in diagnostics and life sciences, is looking for a “Clinical Science Program Specialist (100% Remote)".“Clinical Science Program Specialist (100% Remote)".

Job Duration: Long Term Contract (Possibility Of Extension)

Job Duration: Long Term Contract (Possibility Of Extension)Job Duration: Long Term Contract (Possibility Of Extension)

Pay Rate : $35/hr on W2

Pay Rate : $35/hr on W2Pay Rate : $35/hr on W2

Company Benefits: Medical, Dental, Vision, Paid Sick leave, 401K

Company Benefits:Company Benefits:Medical, Dental, Vision, Paid Sick leave, 401K

Coordinate and manage multiple clinical testing and laboratory services projects from initiation through completion, serving as the primary point of contact for pharmaceutical clients. Drive cross-functional project execution, oversee sample workflow activities, and ensure timely, accurate delivery of clinical study results in a regulated environment.

Coordinate and manage multiple clinical testing and laboratory services projects from initiation through completion, serving as the primary point of contact for pharmaceutical clients. Drive cross-functional project execution, oversee sample workflow activities, and ensure timely, accurate delivery of clinical study results in a regulated environment.

Key Responsibilities:

Key Responsibilities:Key Responsibilities:

• Manage multiple clinical testing and lab services projects under the guidance of the Program Manager.

Manage multiple clinical testing and lab services projects under the guidance of the Program Manager.

• Develop project plans, timelines, and coordinate cross-functional activities to ensure on-time execution.

Develop project plans, timelines, and coordinate cross-functional activities to ensure on-time execution.

• Monitor project progress, identify risks and bottlenecks, and implement solutions to maintain milestones.

Monitor project progress, identify risks and bottlenecks, and implement solutions to maintain milestones.

• Oversee sample processing workflows and ensure accurate reporting of results.

Oversee sample processing workflows and ensure accurate reporting of results.

• Serve as the primary liaison for pharmaceutical clients, CROs, site investigators, and internal stakeholders.

Serve as the primary liaison for pharmaceutical clients, CROs, site investigators, and internal stakeholders.

• Coordinate meetings, prepare agendas, document minutes, and communicate project updates.

Coordinate meetings, prepare agendas, document minutes, and communicate project updates.

• Track and maintain project reports and clinical study data.

Track and maintain project reports and clinical study data.

• Promote best practices and continuous improvement across clinical operations.

Promote best practices and continuous improvement across clinical operations.

Qualifications:

Qualifications:Qualifications:

• Bachelor’s degree required; Life Sciences preferred.

Bachelor’s degree required; Life Sciences preferred.

• 2+ years of project coordination, clinical trial coordination, or project management experience in the CRO, diagnostics, pharmaceutical, or regulated industry.

2+ years of project coordination, clinical trial coordination, or project management experience in the CRO, diagnostics, pharmaceutical, or regulated industry.

• Exposure to clinical studies and regulated documentation.

Exposure to clinical studies and regulated documentation.

• Strong organizational, communication, and collaboration skills.

Strong organizational, communication, and collaboration skills.

• Ability to manage multiple projects in a fast-paced environment.

Ability to manage multiple projects in a fast-paced environment.

Preferred Qualifications:

Preferred Qualifications:Preferred Qualifications:

• Experience with companion diagnostics (CDx), clinical testing, or biosample management.

Experience with companion diagnostics (CDx), clinical testing, or biosample management.

• Knowledge of clinical trial management processes and PMI methodologies.

Knowledge of clinical trial management processes and PMI methodologies.

• Experience within the diagnostics or pharmaceutical industry.

Experience within the diagnostics or pharmaceutical industry.

If interested, please send us your updated resume at

If interested, please send us your updated resume at

[email protected]/[email protected]

[email protected]/[email protected]@[email protected]'m interested{{criteriaIndex}} {{field}} {{captialize(condition)}} ( ) {{cxPropHelpText}} {{cxPropField.consent_details.description}} {{record.Posting_Title}} {{record.Posting_Title}} {{record.Posting_Title}} {{candidate.Email}} {{topMessage}} Job Details {{topMessage}} previous next {{title}} {{score}}% Job Description {{unescape(sanitizeHTML(descriptionHTML))}} {{message}} Step {{curStepInMandatorySecPrompt}}/{{totalNumOfStepsInMandatorySecPrompt}} For privacy and security purposes, please go through the following points and provide consent. Accept Decline {{getI18n("zr.careers.publicpage.meta.joblisting")}} {{getI18n("zr.careers.publicpage.meta.joblisting")}} {{cxPropAssessment.name}} {{getI18n("zr.questionnaire.question.information.heading")}} {{getI18n("zr.cw.autofill.head")}} {{cxPropBodyMessage}} {{getI18n("zr.careers.autopopulate.success")}} {{getI18n("zr.cw.apply.sign",cxPropCompanyInfo.name)}} {{if(cxPropDetails.applyWithSeekButton,cxPropDetails.applyWithSeekButton.buttonLabel,getI18n("zr.quickapply.apply.toggle","Seek"))}} {{getI18n('zr.eeo.questionnaire.portal.maintitle')}} {{botName}} {{getI18n("zr.zia.sb.consent.msg1")}}{{criteriaIndex}}{{criteriaIndex}}{{field}} {{captialize(condition)}}{{field}}{{captialize(condition)}}( )(){{cxPropHelpText}}{{cxPropHelpText}}{{cxPropField.consent_details.description}}

{{cxPropField.consent_details.description}}

{{record.Posting_Title}}{{record.Posting_Title}}{{record.Posting_Title}}

{{record.Posting_Title}}

{{record.Posting_Title}}{{record.Posting_Title}}

{{record.Posting_Title}}

{{record.Posting_Title}}

• {{record.Posting_Title}}

{{record.Posting_Title}}

{{record.Posting_Title}}{{candidate.Email}}{{candidate.Email}}{{candidate.Email}}

{{candidate.Email}}

{{topMessage}}Job DetailsJob DetailsJob DetailsJob Details{{topMessage}}previousnext{{title}} {{score}}% Job Description {{unescape(sanitizeHTML(descriptionHTML))}}{{title}} {{score}}% Job Description {{unescape(sanitizeHTML(descriptionHTML))}}{{title}} {{score}}%

{{title}}

{{title}}{{score}}%Job Description {{unescape(sanitizeHTML(descriptionHTML))}}

Job Description

{{message}}

Step {{curStepInMandatorySecPrompt}}/{{totalNumOfStepsInMandatorySecPrompt}}

For privacy and security purposes, please go through the following points and provide consent.Accept DeclineAccept DeclineAcceptDecline{{getI18n("zr.careers.publicpage.meta.joblisting")}}{{getI18n("zr.careers.publicpage.meta.joblisting")}}

• {{getI18n("zr.careers.publicpage.meta.joblisting")}}

{{getI18n("zr.careers.publicpage.meta.joblisting")}}{{getI18n("zr.careers.publicpage.meta.joblisting")}}{{getI18n("zr.careers.publicpage.meta.joblisting")}}

• {{getI18n("zr.careers.publicpage.meta.joblisting")}}

{{getI18n("zr.careers.publicpage.meta.joblisting")}}{{cxPropAssessment.name}} {{getI18n("zr.questionnaire.question.information.heading")}}{{cxPropAssessment.name}} {{getI18n("zr.questionnaire.question.information.heading")}}{{cxPropAssessment.name}}

{{getI18n("zr.questionnaire.question.information.heading")}}

{{getI18n("zr.cw.autofill.head")}} {{cxPropBodyMessage}} {{getI18n("zr.careers.autopopulate.success")}}

{{getI18n("zr.cw.autofill.head")}}

{{cxPropBodyMessage}}

{{getI18n("zr.careers.autopopulate.success")}}

{{getI18n("zr.cw.apply.sign",cxPropCompanyInfo.name)}}

{{getI18n('zr.eeo.questionnaire.portal.maintitle')}}{{botName}}{{botName}}{{getI18n("zr.zia.sb.consent.msg1")}}{{getI18n("zr.zia.sb.consent.msg1")}}{{getI18n("zr.zia.sb.consent.msg1")}}{{getI18n("zr.zia.sb.consent.msg1")}}{{getI18n("zr.zia.sb.consent.msg1")}}{{getI18n("zr.zia.sb.consent.msg1")}}{{getI18n("zr.zia.sb.consent.msg1")}}