Associate Director, Clinical Site Budgets & Payments
$170k - $190kJade Biosciences
Associate Director, Clinical Site Budgets & Payments Boston; Chicago; San Francisco; Seattle About Jade Biosciences Jade Biosciences is a clinical-stage biotechnology company focused on developing best-in-class therapies that address critical unmet needs in autoimmune diseases. Jade’s lead candidate, JADE101, targets the cytokine APRIL, and is currently being evaluated in a Phase 1 clinical trial for the treatment of immunoglobulin A nephropathy. Jade’s pipeline also includes JADE201, an afucosylated anti-BAFF-R monoclonal antibody, as well as JADE301, an undisclosed antibody candidate, both currently in preclinical development.Jade was launched based on assets licensed from Paragon Therapeutics, an antibody discovery engine founded by Fairmount. For more information, visit JadeBiosciences.com and follow the Company on LinkedIn. Role Overview The Associate Director, Clinical Site Budgets & Payments will architect and lead the company’s global approach to clinical trial site budgeting, investigator grant strategy, transparency compliance, and site/vendor payment governance across our clinical trial portfolio. This leader will define Jade’s global investigator grant philosophy, including structured opening offer and negotiation parameters that ensure speed, fairness, and alignment with global FMV benchmarks. They will establish standards for invoiceables, conditional procedures, pass‑through costs, and country‑specific budgeting norms that apply across all Jade clinical studies. This role oversees a full-service CRO partner responsible for operational execution of budgets, payments, reconciliation, and study financial controls. It also builds and maintains global site budget forecasts, ensures just-in-time CRO funding, and supports accruals, reconciliation, and inspection-readiness. The successful candidate must be equally fluent in clinical trial protocols and financial statements, highly skilled in influencing cross-functional and vendor partners, and able to uphold strict compliance with FMV and Sunshine/Open Payments regulations. This is a high‑visibility, individual‑contributor role reporting directly to the Executive Director, Development Outsourcing and operating globally across all Jade studies. The position is remote, with domestic travel up to four times per year. Key Responsibilities Global Payment Philosophy, Compliance & Governance Define Jade’s global investigator grant strategy, including opening-offer tiers, decision and negotiation parameters, aligned with international FMV standards. Establish and maintain policies for invoiceables, pass-throughs, conditional procedures, screen-fail handling, and complex visit structures; ensure global consistency. Develop and maintain SOPs/WIs governing budgeting, payments, documentation, and global transparency requirements (e.g., U.S. Sunshine/Open Payments and ex-US equivalents). Define FMV justification expectations and ensure audit-ready documentation across all investigator/HCP engagements. Study-Level Budget Design & Financial Oversight Translate clinical protocols into country-specific and site-level cost models that accurately reflect procedures, visit schedules, and conditional events. Build and maintain global study budget forecasts, partnering closely with Clinical Operations and Finance to ensure alignment with development plans. Oversee accruals, spend tracking, payment reconciliation, and close-out documentation for accuracy and inspection readiness. CRO Governance & Issue Escalation Serve as Jade’s primary owner of CRO performance for site budgets and payments, including contract expectations, KPIs, and service delivery standards. Lead the payment-related components of CRO governance forums, including issue resolution, aging analysis, cycle-time performance reviews, and payment forecasting. Resolve escalated site payment issues, driving sustainable root-cause solutions and process improvements. HCP/KOL Payment Operations (“White-Glove” Model) Implement a high-touch service model for KOL/HCP payments (consulting, advisory boards, speaking engagements), ensuring accuracy, speed, and FMV alignment. Streamline administrative burden for external experts by simplifying processes, documentation, and support. Cross-Functional Leadership & Decision Support Partner closely with Clinical Operations, Development Outsourcing, Legal, Compliance, and Finance to ensure budgets and payments reflect protocol intent, operational realities, and compliance needs. Provide executive-level visibility into performance metrics such as payment timeliness, disputes, forecast accuracy, and CRO funding utilization. Serve as Jade’s internal subject-matter expert for investigator/HCP budgeting and payment strategy across a global two-program portfolio in Autoimmune disease. Qualifications Bachelor’s degree in finance, life sciences, business, or related field with 13+ years of experience or an advanced degree (MBA, MS, MPH) with 10+ years of experience. 10+ years of relevant experience in biotech/pharma or CRO roles with direct responsibility for site budgeting and payment oversight Demonstrated ability to interpret clinical protocols and convert them into robust, compliant global site budgets Strong understanding of global FMV frameworks and Sunshine/Open Payments transparency requirements. Proven experience governing a full service CRO, including KPI management, escalation handling, and process improvement. Ability to analyze financial statements, accruals, and cash flow impacts. Excellent communication, negotiation, and cross functional influence. Experience supporting Autoimmune or immune mediated diseases preferred. Experience managing global payment models across diverse regulatory environments preferred. Exposure to KOL/HCP engagement processes with FMV and transparency considerations preferred. Position Location This is a remote role; periodic travel to team and company events is required. The anticipated salary range for candidates for this role is $170,000 - $190,000. The final salary offered will depend on several factors, which may include, but not limited to, relevant years of experience, educational background, and geography. As part of the I-9 verification of authorization to work in the United States, Jade Bioscience participates in E-Verify. To learn more about E-Verify please review this poster. Jade Biosciences is proud to be an Equal Opportunity employer. All qualified applicants will receive consideration for employment without regard to sex, gender identity, sexual orientation, race, color, religion, national origin, disability, protected Veteran status, age, or any other characteristic protected by law. #J-18808-Ljbffr Jade Biosciences
$170k - $190k
About Jade Biosciences Jade Biosciences is a clinical‑stage biotechnology company focused on developing best‑in‑class... ...follow the Company on LinkedIn. Role Overview The Associate Director, Clinical Site Budgets & Payments will architect and lead the company’s global...WebsiteContract workRemote work$170k - $190k
A leading biotechnology company is seeking an Associate Director for Clinical Site Budgets & Payments to manage the global budgeting strategy for clinical trials. This remote role requires expertise in financial analysis, negotiation, and compliance with FMV standards....WebsiteRemote job$211.91k - $256.79k
...words that are usually associated with a job. But... ...with-us. The Associate Director, Global Clinical Science reports through... ...with Medical Writing) Site-facing activities... ...development of trial budget, CRO scope of work, etc... ...We will never request payments, financial information...WebsiteHourly payFull timeTemporary workPart timeFor contractorsSummer workLive inWork at officeLocal areaRemote workFlexible hoursShift work$198.5k - $311.85k
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...you to shine? Join us as an Associate Medical Director in our Neuroscience... ...leads and drives strategy for clinical studies within the overall... ...and size, and influences the budget of all aspects of a study or... ...various meetings or client sites, including overnight trips....WebsiteWork at officeImmediate startRemote workNight shift- ...you to shine? Join us as an Associate Medical Director in our Neuroscience... ...leads and drives strategy for clinical studies within the overall... ...and size, and influences the budget of all aspects of a study or... ...various meetings or client sites, including overnight trips....WebsiteWork at officeImmediate startRemote workNight shift
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...a team of scientists supporting oncology clinical development programs. You will be the primary... ...within commuting distance and work on-site an average of 2.5 days per week. The... ...future. Sunshine Act Pfizer reports payments and other transfers of value to health care...WebsitePermanent employmentH1bLocal areaVisa sponsorshipWork visaRelocation package2 days per week- Job Description Associate Medical Director in Neuroscience Therapeutic Area Unit,... ...leads and drives strategy for clinical studies within global... ...scope, complexity, size and budget, and maintains a state‑of‑the... ...fly to meetings or client sites, including overnight trips....WebsiteLocal areaNight shift
$273.21k - $331.06k
...aren’t words that are usually associated with a job. But working at... ...The Associate Director, Global Clinical Physician sits within Clinical... ...Holds responsibility for site interactions in partnership... ...Protection We will never request payments, financial information, or...WebsiteHourly payFull timeTemporary workPart timeFor contractorsSummer workLive inWork at officeLocal areaRemote workFlexible hoursShift work- ...operational management of complex clinical supply activities across all... ...to global clinical trial sites. This role collaborates with... ...supply chain services. Develop budget and track invoices to... ...Assurance & Regulatory on activities associated with labelling, packaging,...WebsiteFlexible hours
$189.2k - $315.4k
...The Clinical Development Medical Director (Associate Director) is responsible for medical and scientific... ...from investigator sites Medical issues in... ...milestones according to budgets and priorities Effective... ...Act Pfizer reports payments and other transfers of value...WebsitePermanent employmentInternshipH1bLocal areaVisa sponsorshipWork visaRelocation package$170k - $200k
...BlueRock Therapeutics LP is a clinical stage cell therapy... ...Operations Study Lead (COSL)/Associate Director oversees the management and... ...ensuring adherence to timelines, budgets, and quality standards. Develops... ...but not limited to site identification/qualification...Website$141.5k - $268.5k
...manages and communicates multi-disciplinary Clinical Pharmacology development plans and... ...account details, social security numbers, or payment of any kind) during the recruitment process... ...Where We Work Role is primarily site- or office-based but can occasionally be...WebsiteWork at officeImmediate startRemote workMonday to Friday- ...growing, science‑driven biopharmaceutical company is seeking an Associate Director, Clinical QA to play a key role in ensuring GCP compliance across... ...Lead, conduct, and/or oversee GCP audits of clinical sites, vendors, internal systems, and clinical documentation supporting...Website
$175.8k - $237.8k
...Overview: The Associate Director in Clinical Pharmacology position will support a rapidly expanding clinical portfolio of promising RNAi therapeutics... ...external expert consultants, CRO partners and academic sites to problem solve and develop scientific solutions to...WebsiteFull timeTemporary workLocal areaFlexible hours$160.8k - $201k
About the Role The Associate Director, Quantitative Clinical Pharmacology is responsible for providing translational, clinical pharmacology, and pharmacometrics... ...Details Hybrid position: expected to work on site at one of Sarepta’s facilities in the United States and...Website$194k - $267k
...and muscle diseases from early to late-stage clinical development. As a member of the team, the associate medical director will work on late-stage SMA drug and device programs... ...to travel to scientific meetings and clinical sites occasionally as needed (domestic and...WebsiteTemporary workLocal area$170k - $190k
A leading biotechnology company is seeking an Associate Director to oversee global clinical site budgeting and payment strategies. This remote role requires expertise in financial regulations and cross-functional collaboration in the biotechnology sector. Candidates should...WebsiteRemote work$273.21k - $331.06k
...Associate Director, Global Clinical Physician, Neuroscience Working with Us Challenging. Meaningful. Life-changing. Those aren't words that are usually... ...including eligibility review Holds responsibility for site interactions in partnership with the Global Clinical...WebsiteHourly payFull timeTemporary workPart timeFor contractorsSummer workWork at officeRemote workWorldwideFlexible hours- ...California.Position SummaryCRISPR Therapeutics is searching for an Associate Director, Clinical Scientist to provide scientific input for early and late... ...to support internal and external meetings; e.g., site qualification and initiation, investigator meetings, and training...WebsiteRemote work
$172.67k - $210k
...human health. Role Overview The Clinical Scientist will work closely... ...with study / program medical director and clinical operation team... ...to investigators and clinical site staff Providing guidance and/... ...electronic database, IRT, and associated training documents and review...WebsiteFlexible hoursShift work$159k - $195k
...join our team. What You’ll Do: The Associate Director, Clinical Oversight (ADCO) provides strategic leadership... ...within agreed upon timelines, budget, and quality Oversee the planning and... ...Facilitate resolution of region specific and site management related challenges Acts on...WebsiteFull timeWork at officeLocal areaFlexible hours3 days per week$209.25k - $253.57k
Associate Director, Clinical Pharmacology Company: Bristol-Myers Squibb Req Number: R1601979 Location... ...between Christmas and New Years Day. On‑site Protocol BMS has an occupancy... ...Data Protection We will never request payments, financial information, or social security...WebsiteHourly payFull timeTemporary workSummer workRemote workFlexible hoursShift work- ...POSITION SUMMARY The Associate Director of Operations is a key operational... ...systems and BPS contract/site compliance, while also managing... ...including renewals, audits, payments, and compliance. Serve as... ...approve Operations and HR budgets with the HR Coordinator and...WebsiteContract workSummer workWork at office
$110k - $165k
...Manager, Site Budgets and Contracts, Clinical Operations Who we are: At Agios, we are fueled by connections to transform rare diseases. We foster an inclusive, collaborative culture - one that sparks bold thinking and strengthens our connections with each other...WebsiteContract workTemporary workLocal areaRemote workWork from homeFlexible hours3 days per week$110k - $165k
Agios Pharmaceuticals is seeking a Manager for Site Budgets and Contracts to enhance their clinical operations. This role focuses on clinical site contracting, negotiation, and execution of budgets, partnering with CROs and internal teams. Applicants should have a Bachelor...WebsiteRemote jobFlexible hours$185k - $260k
...Position Overview: Beam is seeking an experienced Clinical Quality professional at the Associate Director / Director level to join our grown Quality Team. Reporting... ...level risk-based audit plan, including investigator site, vendor and internal process audits. Provide...WebsiteFull time$166.85k - $181.56k
...integral part of the CQA team and provides oversight for and participates in, auditing services in support of Alkermes Clinical Programs by conducting clinical site, vendor qualification, internal systems and document audits to ensure compliance with cGCPs. The CQA Manager...WebsiteContract workWork at officeLocal areaImmediate startRemote work- ...Associate Medical Director – Inpatient Informatics The Associate Medical Director – Inpatient Informatics... ...health system. This role guides clinical standards, optimizes EHR workflows,... ...specialty, training, and departmental budget. The above hiring range represents a...WebsiteFor contractorsFixed term contractLocal areaImmediate startNight shift
- ...Job Title: Associate Medical Director Location: Cambridge, MA (Remote) Duration: 12 months+... ...Purpose: Provides medical oversight of clinical trials to ensure company SOPs, client... ...outcomes events reported by study sites. Performs data review as specified...WebsiteContract workRemote workShift work
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