What are the responsibilities and job description for the Site Contracts Manager position at Lifelancer?
Job Title : Site Contracts Manager
Job Location : United States
Job Location Type : Remote
Job Contract Type : Contract
Job Seniority Level : Entry level
Catalyst Clinical Research provides customizable solutions to the biopharmaceutical and biotechnology industries through Catalyst Oncology a fullservice oncology CRO and multitherapeutic global functional and CRO services through Catalyst Flex. The company's customercentric flexible service model innovative technology expert team members and global presence advance clinical studies. Visit CatalystCR.com.
As the Site Contracts Manager (SCM I) you are a key member of the Development Operations Central Site Services Team and is responsible for contract and budget development and negotiation with clinical sites acting as a study functional lead for the Central Site Services team. The SCM I works directly with the Project Manager Clients vendors and other internal functional teams to ensure quality deliverables ontime and onbudget. Our mission is for our Catalyst staff to operate seamlessly with our customer teams using the Catalyst site centric model to enhance employee satisfaction while giving the sites and customers the reassurance that they have a strong and experienced team.
Position Responsibilities
Clinical Trial Responsibilities and Accountabilities :
- Prepares budget templates for amendment.
- Prepares contract templates.
- Prepares payment language terms.
- Establishes negotiation parameters with sponsors.
- Collaborates with Site Activation Manager to develop start up strategy plan.
- Negotiates contracts and budgets with clinical sites.
- Tracks negotiation progress identifies operations issues and escalates issues to the attention of the Project Manager or line manager.
- Interfaces with Sponsor representatives and internal project team.
- Responsible for filing of fully executed contracts per sponsor agreements.
- Transfers fully executed contract to site payment group.
- Escalate study issues appropriately and in a timely manner.
- Responsible for understanding the CSS budget on each project and the actions required to maintain it.
- Collaborates and supports the project team with amendments to the site contract and site budget as needed.
- Assists with department activities and initiatives as appropriate (e.g. process improvement).
Project Oversight And KPI Responsibilities
Process Development Responsibilities
QA And Study Audit Responsibilities
Position Qualifications
Education : Bachelor’s degree or equivalent education in a related field of study.
Experience : At least 1 years in pharmaceutical research field (CRO pharma site etc.) and 1 year of applicable industry experience negotiating contracts and budgets.
Required Skills
Applicants must be authorized to work for ANY employer in the U.S. We are unable to sponsor or take over sponsorship of an employment visa.
Lifelancer ( ) is a talenthiring platform in Life Sciences Pharma and IT. The platform connects talent with opportunities in pharma biotech health sciences healthtech and IT domains.
For more details and to find similar roles please check out the below Lifelancer link.
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Key Skills
Facilities Management,ADMA,Heavy Bus Driving,AXA,Building Services,Courier Delivery
Employment Type : Full Time
Vacancy : 1