The team behind your protocol

Clinical expertise.
Clear study responsibilities.

Our research teams bring together the clinical, operational, and participant support your protocol requires, with coordinated roles from study preparation through follow-up.

Clinical care

Principal Investigators & Sub-Investigators

Clinical oversight, eligibility review, safety assessments, and specialty expertise aligned with the protocol.

Nursing & Clinical Support

On-site nursing supports clinical procedures, delegated treatment administration, and participant observation.

Dietitian & Nutrition Support

Nutrition assessments, dietary education, and counseling through on-site, remote, or sponsor-provided central dietitians.

Counseling & Behavioral Support

On-site participant education, lifestyle counseling, and licensed mental-health support, including psychiatry.

Study execution

Clinical Research Coordinators

Visit coordination, protocol workflows, source documentation, and participant follow-up.

Phlebotomy & Laboratory Staff

Blood collection, PK sampling, specimen processing, storage, and preparation for central-laboratory shipment.

Investigational Product Staff

Product preparation, dispensing, accountability, and storage, with assigned blinded and unblinded responsibilities.

Network support

Dedicated Recruitment Team

Centralized outreach, prescreening, referral coordination, and recruitment follow-up alongside the clinical team.

Regulatory & Startup Support

Essential documents, IRB coordination, training records, and study activation requirements.

Data & Monitoring Support

EDC entry, query follow-up, source preparation, and coordination of on-site and remote monitoring.

Quality & Operations Oversight

Standardized SOPs, weekly team quality reviews, issue follow-up, and coordination of study resources.

Study assignments, training, coverage, and visit capacity are reviewed against the protocol.

Explore investigator expertise

Clinical resources

The capabilities
your protocol calls for.

Explore our network resources. Procedure requirements, specialty access, equipment specifications, and scheduling are confirmed during feasibility.

Clinical assessments & procedures

  • 12-lead and triplicate ECGs
  • Vital signs, calibrated scales, and anthropometric measurements
  • Skin biopsy and clinical photography
  • Dermatology assessments: EASI, vIGA-AD, PASI, and DLQI
  • Protocol-required clinical and behavioral assessments

Laboratory & sample support

  • Blood, urine, and protocol-specific specimen collection
  • Ambient and refrigerated centrifugation
  • Sample separation, aliquoting, and labeling
  • Refrigerated and frozen specimen storage
  • Dry ice access and central-laboratory shipment coordination
  • IATA-trained laboratory & shipping personnel
    Our laboratory and shipping personnel maintain current IATA training for their responsibilities, with renewal as required. This supports proper specimen packaging, labeling, documentation and shipment.

IP handling & administration

  • Preparation, dispensing, and product accountability
  • Secure, temperature-controlled IP storage
  • Infusion, injection, and biologic administration
  • Assigned blinded and unblinded workflows
  • Product reconciliation and destruction coordination

Imaging & specialty access

  • Endoscopy with protocol-required biopsy
  • CT, MRI, X-ray, and ultrasonography
  • Echocardiography and DXA access
  • Eye examinations and fundus photography
  • Specialist procedures reviewed against protocol needs

Specialty services are coordinated with qualified providers; location and scheduling are confirmed during feasibility.

Equipment & storage readiness

  • Equipment calibration and maintenance documentation
  • Continuous temperature monitoring
  • Controlled ambient, refrigerated, and frozen storage
  • Backup storage arrangements
  • Emergency equipment and supplies

Required temperature ranges, backup arrangements, and equipment specifications are reviewed for each protocol.

Visit & monitoring capacity

  • Private examination and treatment spaces
  • Extended observation and intensive sampling, where supported
  • Dedicated monitoring and meeting space
  • Secure document and record storage
  • Participant reception and coordinator workspaces

Staffing, visit duration, and sampling schedules are assessed against study requirements and available capacity.

PK collection & sample processing

Every collection.
Every handling step.

Protocol-specific collection and processing connect the study visit to the designated laboratory, with attention to timing, handling conditions, and documentation.

  • Collection planningScheduled PK draws, collection-time documentation, and visit planning around required sampling windows.
  • Protocol-specific processingCentrifugation, separation, aliquoting, and labeling according to the laboratory manual.
  • Storage and shipmentRequired storage conditions, sample tracking, shipment preparation, and central-laboratory coordination.

Intensive sampling and extended observation are evaluated against the collection schedule and available clinical capacity.

Technology-enabled operations

Connected records.
Supported study teams.

Clinical information and study systems support feasibility, visit coordination, documentation, and sponsor oversight across the network.

Connected clinical information

Private-practice patient access and connected EMR data inform protocol-specific feasibility and clinical review.

  • EMR-informed patient assessment
  • Coordinated study information

Study systems & data

Teams work with sponsor-required systems for study data, treatment allocation, and participant-reported information.

  • EDC and query follow-up
  • IRT and electronic questionnaires

Monitoring & source access

On-site monitoring space and secure remote source access support authorized review, with access arranged for each study.

  • On-site and remote monitoring
  • Source preparation and follow-up

Standardized procedures and weekly team quality reviews support consistent execution.

Explore quality & compliance

Inside our research spaces

Built for study visits.
Ready for collaboration.

Clinical, laboratory, and meeting spaces support the practical work of a research visit. Select a photo for a closer look.

Private consultation room with a desk and examination bed in Miami Lakes

Private consultation space

Miami Lakes · A private setting for participant discussions and clinical visits.

Recliner, examination bed, and clinical equipment in Miami Lakes

Infusion & clinical equipment

Miami Lakes · Treatment and observation space with clinical equipment.

Staff member handling specimen tubes at a Miami Lakes laboratory counter

Sample processing & collection

Miami Lakes · Specimen preparation in our clinical laboratory.

Meeting table and chairs at WCR’s Miami Lakes facility

Monitoring & meeting space

Miami Lakes · A setting for monitor review and study-team discussions.

Therapeutic expertiseExplore our clinical experienceRecruitment & retentionSee how we support participationFeasibility & startupPlan the path to activation

Start with your protocol

Let us assess fit for your study.

Share the procedures, patient population, sampling schedule, and operational requirements. Our team will review the resources and support your study needs.

Request Site Evaluation Contact Our Team