As a trusted staffing and recruitment partner, we are committed to connecting you with the perfect opportunity at a global leader in biotechnology. Leveraging our extensive network, we provide access to top-tier roles that allow you to grow and make a meaningful impact in the healthcare and life sciences industries. This company is dedicated to discovering and developing innovative therapies that address serious diseases, with a focus on oncology, cardiology, and bone health. With a strong legacy of scientific excellence and a mission to improve patient outcomes worldwide, they offer a dynamic environment where your contributions will drive real change. If you're seeking a rewarding career that makes a difference, let us help you take the next step!
location: Telecommute
job type: Contract
salary: $40.00 - 64.29 per hour
work hours: 9 to 5
education: Bachelors
responsibilities:
- Negotiate clinical site contracts (i.e. Disclosure Agreements, Clinical Trial Agreements, Service Agreements) using appropriate guidelines and collect necessary signatures for contract execution; Participate in site/legal/finance meetings as required to resolve contract issues;
- Negotiate site budgets from base budget and payment milestones using appropriate guidelines;
- Escalate contract and budget issues as appropriate;
- Support Clinical Pricing & Payments Group in setting up sites for payment;
- Track contract progression using appropriate systems;
- Amend and terminate contracts as necessary throughout lifecycle of study;
- Store and archive contracts and budgets in appropriate systems;
- Responsible for reviewing and approving, with Law guidance, applicable changes within ICF
- Manage end to end process for clinical site contracts;
- Support resolution of contract and budget issues;
- Maintain tracking in appropriate systems
qualifications:
- Master degree or Bachelors degree and 2 years of pharma experience
- Recent (within last 3 years) contract and budget negotiation experience in a clinical trial setting.
- Active/involved negotiation with various contract types (CTA, CDA, Master Agreements, etc.) and applicable budget.
- Proficient with Microsoft Office programs, with focus on Excel
- Pharma experience
skills: MS-EXCEL, Clinical Study Design, CTMS (Clinical Trial Management Systems), CTA, CTD Structure, Clinical Trial Supply Strategy
Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.
At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact HRsupport@randstadusa.com.
Pay offered to a successful candidate will be based on several factors including the candidate's education, work experience, work location, specific job duties, certifications, etc. In addition, Randstad offers a comprehensive benefits package, including health, an incentive and recognition program, and 401K contribution (all benefits are based on eligibility).
This posting is open for thirty (30) days.
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Qualified applicants in San Francisco with criminal histories will be considered for employment in accordance with the San Francisco Fair Chance Ordinance.
Qualified applicants in the unincorporated areas of Los Angeles County with criminal histories will be considered for employment in accordance with the Los Angeles County's Fair Chance Ordinance for Employers.
We will consider for employment all qualified Applicants, including those with criminal histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles' Fair Chance Initiative for Hiring Ordinance.