Senior Clinical Laboratory Associate — Pharmaceutical; Hybrid — Indianapolis, IN Extension

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

Indianapolis, United States

• Industry Pharma/Biotech/Clinical Research
• City Indianapolis
• State/Province Indiana
• Country United States

From development to commercialization, we partner with Pharmaceutical, Medical Device and Biotechnology clients to provide solutions to complex compliance issues. We collaborate with our partners by providing technical expertise in Quality, Regulatory Compliance and Manufacturing Science and Technology. Our business mission is to ensure our clients exceed their compliance goals while improving patient health and safety. Visit us at  and follow us on Linked In:

Our Fortune 500 global Pharmaceutical client is seeking an experienced Clinical Laboratory Associate.

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.

• 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

Schedule:

40 hours/week

Work Setup:
Hybrid (3 days onsite, 2 days remote – flexible) in Indianapolis, IN

• 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

• 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.

Pharmavise Corporation is an Equal Opportunity Employer and does not discriminate on the basis of race or ethnicity, religion, sex, national origin, age, veteran disability or genetic information or any other reason prohibited by law in employment.