Connecting Talent with Opportunity in Clinical Research

We specialize in bridging top talent with leading organizations and institutions in clinical research. Our expertise spans across data analysis, laboratory support, project management, financial planning, contract negotiations, regulatory compliance, medical affairs and more. We're dedicated to fostering successful partnerships that drive innovation and progress in healthcare."

Clinical Data Coordinators

Tasks Expertise:

  • Enter clinical trial data into EDC (Electronic Data Capture) systems (e.g., Medidata Rave, Oracle InForm).

  • Perform data cleaning and query resolution with sponsors/CROs.

  • Track patient visit data and ensure timely submission to sponsors.

  • Review source documents for completeness and accuracy.

  • Generate and respond to data queries from monitors and data managers.

  • Support database lock and reconciliation processes (e.g., SAE reconciliation).

Budget Analyst

Task Expertise:

  • Develop and negotiate clinical trial budgets with sponsors/CROs.

  • Conduct coverage analysis to distinguish standard of care vs research costs.

  • Track study payments and reconcile site payments with sponsor invoicing.

  • Monitor site expenses and ensure alignment with negotiated budget.

  • Collaborate with CRCs to identify protocol-related procedures and costs.

Regulatory Coordinator

Task Expertise:

  • Prepare and submit IRB/EC applications, amendments, and continuing reviews.

  • Submit safety reports, IND annual reports, and protocol deviations to appropriate bodies.

  • Maintain regulatory binders (investigator files) and ensure compliance.

  • Track FDA, EMA, and local regulatory submission timelines.

  • Coordinate sponsor/regulatory inspections and audits.

Clinical Research Coordinator

Task Expertise:

  • Screen and recruit oncology patients for clinical trials.

  • Obtain informed consent and educate patients on study participation.

  • Coordinate and schedule study visits, labs, imaging, and procedures.

  • Collect and document source data during study visits.

  • Manage investigational product (IP) accountability and storage.

  • Liaise with investigators, sponsors, and monitors during site visits.

  • Report AEs/SAEs and ensure timely follow-up.

Contract Associate

Task Expertise:

  • Review and negotiate clinical trial agreements (CTAs), confidentiality agreements, and other legal documents.

  • Work with sponsors/CROs and internal legal teams to finalize contracts.

  • Ensure alignment between contract terms and budget (e.g., payment terms, indemnification).

  • Track contract timelines and report bottlenecks.

  • Support resolution of contractual disputes during trial execution.