Clinical Research Coordinator Actalent
Overview
Coordinate complex clinical drug trials managing patient visits and recruitment while collaborating with research nurses and data regulatory teams. This role offers strong training structured onboarding and growth opportunities within a cancer center environment.
What You'll Do11
- 1Conduct patient-facing clinical research activities including coordinating and performing patient visits according to study protocols
- 2Work directly with patients to explain study procedures obtain informed consent and ensure understanding of risks benefits and requirements
- 3Collaborate closely with research nurses to plan schedule and execute patient visits and study-related procedures
- 4Participate in patient recruitment efforts using referrals tumor boards and new consults contributing to screening patients based on inclusion exclusion criteria
- 5Perform detailed chart reviews to identify eligible patients verify eligibility and ensure accurate documentation of clinical and research data
- 6Support active studies within the hematology team managing approximately 10 participants ensuring timely follow-up visit coordination and adherence to study schedules
- 7Consent approximately 12–15 patients per year maintaining high standards of ethical conduct and patient-centered communication
- 8Apply clinical skills as needed during patient visits aligning with study protocols and scope of practice
- 9Communicate effectively with multidisciplinary team to ensure even workload distribution and smooth execution of trial activities
- 10Adhere to institutional and study-specific policies procedures and guidelines to maintain compliance and ensure high-quality clinical research
- 11Manage multiple studies balancing defined patient load within structured team environment
Requirements18
- 1At least 1 year of clinical research experience in patient-facing role including consenting patients and conducting patient visits
- 2Experience working on clinical drug trials with some level of complexity in any therapeutic area
- 3Demonstrated experience in patient recruitment identifying potential participants and engaging them in clinical research opportunities
- 4Proven ability to obtain informed consent from patients in clear ethical and compliant manner
- 5Basic understanding of clinical research data and regulatory processes collaborating effectively with specialized data and regulatory teams
- 6Bachelor’s degree
- 7Clinical research certification (or strong commitment to obtain one such as SOCRA or ACRP)
- 8Familiarity with clinical trials processes and terminology
- 9Strong communication and interpersonal skills for direct patient interaction and multidisciplinary teamwork
- 10Ability to manage multiple studies and balance defined patient load within structured team environment
- 11Organizational skills and attention to detail for chart review documentation and protocol timeline adherence
- 12Experience in oncology clinical research
- 13Experience with Phase I clinical trials
- 14SOCRA or ACRP certification or active pursuit of these credentials
- 15Interest in specializing within hematology oncology research
- 16Motivation to grow within structured training and development framework including internal programs and defined career paths
- 17Flexibility to move between different teams within the cancer center or broader health system
- 18Work flexibility including onsite requirement first three months and optional remote work one day per week after initial period
Salary Insight
$56 - $73k per year
Location
Required Skills
Similar open positions
Explore active roles that match your skills and interests.
Actalent
VerifiedSr Clinical Research Coordinator Oncology Actalent
Leadership role overseeing clinical trial execution for oncology studies. Manage full lifecycle of trials while collaborating with physicians and research teams. Seeking proactive professional to drive innovative therapies.
Actalent
VerifiedClinical Research Coordinator Actalent
Lead primary contact with participants sponsors and regulators. Own full lifecycle of studies from initiation to closeout. Drive eligibility determination and consent collection per protocol. Develop recruitment strategies. Oversee specimen collection and data management. Maintain project databases create flow sheets and finalize case reports. Ensure protocol compliance audit case reports and prepare regulatory submissions. Manage IRB renewals assemble study kits monitor procedure scheduling and attend sponsor meetings. Control expenditures and resolve billing issues with finance teams. Collaborate with PI to guarantee patient safety and study integrity. Document all patient and research data appropriately. Oncology Pre-screening patients Chart review Clinical trial Crc Recruitment Edc Patient recruitment
Actalent
VerifiedSr Clinical Research Coordinator Oncology
Lead senior clinical research coordinator overseeing study execution for diverse portfolio of investigator initiated and industry sponsored trials. Seeking proactive research professional passionate about clinical research patient care and driving innovative therapies.
Actalent
VerifiedClinical Trial Specialist, Oncology Research & Coordination
Own and coordinate oncology and hematology clinical trials across multiple sites ensuring adherence to protocols and GCP. Collaborate with research nurses, physicians, sponsors, and patients to support the full trial lifecycle from activation to closeout. Improve study tools, data capture, and regulatory documentation while maintaining high-quality, compliant trial conduct. This role offers exposure to high-volume enrollment and multi-center coordination in a mission-driven cancer research environment.
Actalent
VerifiedClinical Research Assistant, Oncology Trials & Phlebotomy
Onsite clinical research role supporting oncology trials at multiple LA area sites. Own patient visits, data collection, and regulatory tasks to enable study progress on ~45 active trials. This developmental position offers a clear path toward a Clinical Research Coordinator role within a collaborative team.
Actalent
VerifiedResearch Coordinator Actalent Chicago
Research Coordinator at Actalent in Chicago leads participant recruitment and data management for clinical trials. This role drives efficient study execution while ensuring regulatory compliance and high-quality data handling.