Clinical Research Study Startup Jobs in Indiana (NOW HIRING)

Not be trained on study startup activities Requirements * Bachelor's degree required * 6+ years of Clinical Industry experience * 3+ years of Clinical Research Assistant/Coordinator experience

Assists in identifying study related procedures for the project budget. • Administrative Duties: Attends Investigator and Coordinator Meetings as requested by the sponsor along with appropriate ...

* Assists in the conduct of clinical research studies or trials following established protocols and standard operating procedures. * Assists with identifying and recruiting subjects for clinical ...

The CRC will coordinate and support all aspects of clinical trials and research studies, including subject recruitment, data collection, regulatory compliance, and specimen handling. Candidates with ...

The cCLAs would not be trained on study startup activities but would be the single point of contact ... years of Clinical Research Assistant/Coordinator experience • Prior experience in pharma ...

... clinical research studies ... Participates in study budget negotiations and reconciles study budget accounts. * Develops ...

... clinical research studies by supporting budget development, contract administration, financial ... Monitor compliance with contractual payment terms, including startup payments, patient visit ...

The cCLAs would not be trained on study startup activities but would be the single point of contact ... Experience in clinical research or a closely related field * Demonstrated ability to communicate ...

Manages research study inventory and supplies (such as medications, equipment, devices) and ... Society of Clinical Research Associates (SOCRA)/ Association of Clinical Research Professionals ...

Manages research study inventory and supplies (such as medications, equipment, devices) and ... Association of Clinical Research Professionals (ACRP) or Society of Clinical Research Associates ...

Manages research study inventory and supplies (such as medications, equipment, devices) and ... Association of Clinical Research Professionals (ACRP) or Society of Clinical Research Associates ...

Completes clinical study start-up activities including the development of Fast Facts, Device Set-up and document development. Patient Referrals: * Manages new patient referrals to oncology research ...

The cCLAs would not be trained on study startup activities but would be the single point of contact ... Experience in clinical research or a closely related field * Demonstrated ability to communicate ...

The cCLAs would not be trained on study startup activities but would be the single point of contact ... research or a closely related field • Demonstrated ability to communicate clearly • ...

Responsible for performing research procedures according to the study protocol and working in ... Demonstrates compliance with good clinical practice (GCP) and applicable law, and verifies that ...

Evaluates protocol, study design and feasibility for subject population; determines staff and ... OR * Bachelor's degree plus 5 years of clinical research experience including supervisory ...

Relevant experience in clinical research or oncology and/or nursing position related area of specialty Navigation experience preferred (Preferred) • Manages study participant care in clinical ...

Relevant experience in clinical research or oncology and/or nursing position related area of specialty Navigation experience preferred (Preferred) • Manages study participant care in clinical ...

Responsible for the performance of the research study under the medical supervision of the Principal Investigator. Clinical Research Coordinator III (RN) performs tasks independently, consistently ...

Responsible for the performance of the research study under the medical supervision of the Principal Investigator. Clinical Research Coordinator III (RN) performs tasks independently, consistently ...