Senior Contracts and Budget Associate

Precision for Medicine
South Korea +1 more
RemoteCareer-pivot friendly

Who this role is best for

Aimed at mid-to-senior level contract management professionals with clinical research experience who can manage cross-functional collaboration and remote coordination.

Best fit for

  • Candidates with 3+ years in clinical research contract management and strong cross-functional coordination skills
    — “3 years of relevant experience drafting, reviewing and negotiating agreements related to clinical research”
  • Individuals who have worked with internal and external stakeholders in global clinical trial environments
    — “Lead interactions with the North American and European internal study teams, as applicable”
  • Professionals familiar with tracking and maintaining legal agreements and budgets in a remote setting
    — “Support the maintenance of contract files and databases, including email and document archiving”

Things to consider

  • Candidates must be legally authorized to work in their country of employment without employer sponsorship
    — “Candidates must be legally authorized to work in the country of employment without employer sponsorship.”
  • The role involves close coordination with sponsors, sites, and internal teams across multiple regions
    — “Lead interactions regarding the various agreements with the Site(s) and Sponsor(s)”

How to stand out

  • Highlight experience with CDA, CTA, and CTA-A agreements in your resume and interview responses
    — “Prepare and negotiate Agreements/Amendments such as Confidentiality Disclosure Agreements (CDA), Clinical Trial Agreements (CTA) and Amendments (CTA-A)”
  • Showcase your experience in resolving contractual issues with internal and external stakeholders
    — “Work with supervisor and various internal/external stakeholders to resolve contractual issues”
Pace · SteadyCollaboration · HighAutonomy · MediumDecision Impact · Team

Derived from job-description analysis by Serendipath's career intelligence engine.

What success looks like

  • preparing and negotiating agreements
  • leading interactions with internal and external stakeholders
  • resolving contractual issues
  • tracking contract negotiations and execution
  • supporting contract files and databases
Typical background
3 years of relevant experience in contract management, preferably in a clinical research or similar industry setting

Skills & requirements

Required

Contracts And Budget ManagementLegal AgreementsClinical Trial AgreementsSite BudgetsInternal Study Team InteractionsContractual Issues ResolutionCompany Policies And ProceduresContract Files And Databases Management

Preferred

Clinical ResearchLife ScienceBiotechPharmaceutical Industry

Stack & domain

ContractsBudgetsLegal AgreementsConfidentiality Disclosure Agreements (cda)Clinical Trial Agreements (cta)Amendments To The Clinical Trial Agreements (cta-a)Vendor ContractsSite BudgetsClinical OperationsProject TimelinesExpectationsDraftingReviewingNegotiatingTrackingClinical ResearchContract ResearchLife ScienceBiotechPharmaceutical IndustryContract ManagementContract Research Organization (cro)Clinical Trial ExecutionDeep Scientific KnowledgeLaboratory ExpertiseAdvanced Data SciencesOncologyRare DiseaseAgreementsAmendmentsLeadershipCommunicationProblem-solvingTeamworkStrategic ThinkingProject ManagementDecision-makingAttention To DetailOrganizationPrioritizationCollaborationCustomer ServiceTrainingSupportLegalFinanceAdministrationHealthcarePharmaceuticals

About the role

Original posting from Precision for Medicine via Greenhouse

Precision for Medicine is not your typical CRO.  At Precision for Medicine we have brought together new technologies, expertise and operational scale to help the life sciences improve the speed, cost and success rate of bringing life-changing therapies to patients.  What sets us apart is the way we integrate clinical trial execution with deep scientific knowledge, laboratory expertise and advanced data sciences. We have a strong focus on Oncology and Rare Disease.

Precision for Medicine is looking for a Senior Contracts and Budget Associate.

Position Summary:

Review, draft, negotiate and track a variety of legal agreements including confidentiality disclosure agreements (CDA), initial clinical trial agreements (CTA), amendments to the clinical trial agreements (CTA-A), site budgets and other various types of documents. Will work closely with the Clinical Operations study team and play an administrative role to ensure deliverables are in alignment with defined project timelines and expectations.

Essential functions of the job include but are not limited to:

  • Prepare and negotiate Agreements/Amendments such as Confidentiality Disclosure Agreements (CDA), Clinical Trial Agreements (CTA) and Amendments (CTA-A), vendor contracts and site budgets.
  • Lead interactions with the North American and European internal study teams, as applicable
  • Lead interactions regarding the various agreements with the Site(s)
  • Lead interactions regarding assigned agreements with the Sponsor(s)
  • Work with supervisor and various internal/external stakeholders to resolve contractual issues.
  • Ensure adhered to company policies, procedures, and contracting standards.
  • Update relevant study team members and sponsors regarding the status of contract negotiations and execution.
  • Coordinate execution of the agreements
  • Support the maintenance of contract files and databases, including email and document archiving.
  • Other duties as assigned.

Requirements :

  • Bachelor’s degree, or equivalent contract management experience preferably in a clinical research or similar industry setting
  • 3 years of relevant experience drafting, reviewing and negotiating agreements related to clinical research i.e. Non-Disclosure Agreements, Clinical Trial Agreements, etc. as well as management, control and tracking of the contract process.
  • Experience in contract research, life science, biotech or pharmaceutical industry is preferred.

Preferred:

  • Equivalent contract management experience in a clinical research or similar industry setting
  • Experience in contract research, life science, biotech or pharmaceutical industry.

Any data provided as a part of this application will be stored in accordance with our Privacy Policy. For CA applicants, please also refer to our CA Privacy Notice.

Precision Medicine Group is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, age, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status or other characteristics protected by law.

If you are an individual with a disability and require a reasonable accommodation to complete any part of the application process or are limited in the ability or unable to access or use this online application process and need an alternative method for applying, you may contact Precision Medicine Group at myHR@precisionmedicinegrp.com.

Recruitment Fraud Warning: Please be aware that fraudulent individuals and websites may impersonate Precision Medicine Group or its affiliates and attempt to obtain personal, financial, or banking information through fake job postings or employment offers. Precision Medicine Group will never request payment, banking details, or other sensitive financial information as part of the recruitment process. If you believe you have been targeted by a recruitment scam, we encourage you to report the incident to your local law enforcement authorities, consumer protection agency, or relevant cybercrime reporting organization in your country. Please also notify us at myHR@precisionmedicinegrp.com so we can investigate and take appropriate action.

Candidates must be legally authorized to work in the country of employment without employer sponsorship.

Source: Precision for Medicine careers (Greenhouse)

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