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Senior Clinical Laboratory Associate — Pharmaceutical (Hybrid — Indianapolis, IN) Contract (Possible Extension)

Pharmavise Corporation
Posted 20 days ago, valid for 9 days
Location

Indianapolis, IN, US

Salary

Competitive

Contract type

Contract

Health Insurance
Retirement Plan
Paid Time Off
Life Insurance
Disability Insurance
Flexible Spending Account

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Sonic Summary

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  • Our Fortune 500 global Pharmaceutical client is seeking an experienced Clinical Laboratory Associate with a Master’s and/or Ph.D. in the Medical Science field.
  • The position requires 10-15+ years of experience in Project/Program Management, preferably in pharma, diagnostics, or CRO environments.
  • The role involves study level project management, serving as a single point of contact for study teams, and tracking various sample types.
  • The contract length is 12 months with a salary of $80,000 to $100,000, depending on experience, and offers a hybrid work setup in Indianapolis, IN.
  • Benefits include health insurance, a 401(k) plan, commuter benefits, and paid time off, effective after 30 days.
Our Fortune 500 global Pharmaceutical client is seeking an experienced Clinical Laboratory Associate.

Job Summary:
The Clinical Laboratory Services (CLS) currently has a business need for surge capacity coverage for delivery based Clinical Laboratory Associate (cCLA). This surge capacity model would utilize US-based contractor CLAs (cCLAs) to focus on specific tasks/deliverables. The cCLAs would not be trained on study startup activities but would be the single point of contact representing CLS to study teams and TPOs throughout study maintenance and closeout.

Key Responsibilities:
• Study level project management – including maintenance, data lock and closeout, document flow (review/approvals), budget management
• Single point of contact for study teams and CLS TPOs
• Tracking of safety, biomarker, PK and ADA samples as well as imaging and connected devices
• Query tracking and management
• Internal & External Engagement - Collaborate with internal business partners regarding CLS processes and business operations
• Collaborate with business partners and TPOs to ensure data delivery

Other Details:
Schedule: 40 hours/week
Work Setup: Hybrid (3 days onsite, 2 days remote – flexible) in Indianapolis, IN
Contract Length: 12 months – w/ possible extension

Requirements

Required Qualifications:
• Master’s and/or PH.D degree in the Medical Science field
• 10-15+ years of experience in the Project/Program Management field
• Prior experience in pharma, diagnostics or CRO environment
• Experience in clinical research or a closely related field
• Demonstrated ability to communicate clearly
• Demonstrated attention to detail and organization
• Skilled in excel for report combining and tracking


Benefits

Benefits:
• Health Insurance: Eligibility to enroll in medical, dental, and vision insurance plans. You may also participate in a Flexible Spending Account (FSA) or Health Savings Account (HSA) for qualified healthcare and dependent care expenses.
• Voluntary Benefits: Option to enroll in employee-paid voluntary benefits, including life insurance, short- and long-term disability insurance, and long-term care insurance.
• 401(k) Plan: Eligibility to participate in the company’s 401(k) retirement plan. Please note, this plan does not include an employer contribution.
• Commuter Benefits: Eligibility to participate in a commuter benefits program, allowing the use of pre-tax dollars for transit and/or parking expenses.
• Paid Time Off (PTO): You will accrue two weeks of vacation annually (prorated based on your start date), in addition to sick leave accrued in accordance with applicable state laws. You will also receive 11 company-paid holidays each year.

Note: Benefits will be effective after 30 days.





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