Clinical Research Coordinator (Carlsbad, CA)

Profound Research; California (MO); On-site; USD 70,000 - 90,000; Full time

Job summary

A leading company in clinical research is seeking a Clinical Research Coordinator to manage trial activities, mentor staff, and ensure compliance with protocols. This role requires strong attention to detail and effective communication with various stakeholders.

Qualifications

• 2 years relevant experience in the life science industry.
• Successful completion of GCP certification and CCRC certification within 6 months.

Responsibilities

• Manage all clinical trial activities in compliance with protocols.
• Mentor and train staff in clinical trials and trial management.
• Ensure good documentation practices for clinical trial data.

Skills

Attention to Detail

Communication

Organization

Team Player

Education

Bachelor’s degree

Associate’s degree

High School Graduate

Job description

Clinical Research Coordinator (Carlsbad, CA)

Join to apply for the Clinical Research Coordinator (Carlsbad, CA) role at Profound Research

Clinical Research Coordinator (Carlsbad, CA)

2 weeks ago Be among the first 25 applicants

Join to apply for the Clinical Research Coordinator (Carlsbad, CA) role at Profound Research

Profound Research

Profound Research seeks to drive clinical innovation by partnering with community physicians to offer clinical research as a therapeutic option to their patients. Profound enables providers with the right people and tools to launch clinical research operations, often for the first time, to offer new care pathways to patients. Profound Research is looking to grow its energetic team inspired by changing how patients and providers engage in clinical research.

Profound Research

Profound Research seeks to drive clinical innovation by partnering with community physicians to offer clinical research as a therapeutic option to their patients. Profound enables providers with the right people and tools to launch clinical research operations, often for the first time, to offer new care pathways to patients. Profound Research is looking to grow its energetic team inspired by changing how patients and providers engage in clinical research.

Our Mission: Improving Lives by Providing Advanced Therapeutic Options

Our Vision: Creating the Absolute Best Patient-Physician Experience in Clinical Research

Our Values

Compassion: We value the patient-physician relationship above all else and are committed to a service-oriented approach to all interactions.

Urgency: We work hard and practice selflessness, acting swiftly and decisively to meet the needs of our patients, partners, and colleagues.

Solution Orientation: We are relentlessly positive, and we communicate directly to efficiently identify and implement effective solutions.

Excellence: We insist on excellence, holding ourselves accountable and empowering each other to deliver best-in-class service while maintaining the highest ethical and scientific standards.

Profound Ethos

• Physicians are the Vanguard
• All Decisions Improve Patient Care
• Never Compromise Quality
  
  

Why this Role Exists

The Clinical Research Coordinator will manage all clinical trial activities under supervision in compliance with all applicable laws, regulations, and procedures of study protocol while maintaining company mission, vision and values.

Responsibilities

• Conduct and manage all clinical trial activities in accordance with established research protocols and standards in compliance with all applicable laws, regulations, policies, and procedural requirements.
• Complete all relevant Profound Research required training, including but not limited to ICH-GCP certification and IATA certification in a timely manner.
• Mentor and train staff in the conduct of clinical trials, protocol requirements, communication and trial management skills.
• Lead, implement and coordinate duties for assigned clinical trials including but not limited to study start up, vendor management, subject recruitment, source document review and completion, protocol training, collection of regulatory documents, participant visits, timely data collection and documentation, management and reporting of adverse events, serious adverse events, and deviations, and monitoring visits and follow up.
• Ensure good documentation practices are applied by all team members when collecting, maintaining and correcting study data and required records of clinical trial activity including but not limited to source documentation, case report forms, queries, drug dispensation records, and regulatory forms.
• Communicate effectively and professionally with coworkers, leadership, study subjects, sponsors, CROs, and vendors.
• Collect and account for supplies from sponsors such as lab kits, ancillary supplies, and investigational products.
• Other duties as assigned.
  
  

Requirements

• Bachelor’s degree and 2 years relevant experience in the life science industry OR
• Associate’s degree with 4 years relevant experience in the life science industry OR
• High School Graduate and/or technical degree with minimum of 6 years relevant experience in the life science industry AND 1 year
• Clinical Research Coordinator experience
• Successful completion of GCP certification and Certified Clinical Research Coordinator (CCRC) certification within 6 months of being in the role
• Experience performing clinical assessments, including but not limited to obtaining vital signs, EKGs, blood draws, processing/shipping lab specimens
• Proficient ability to work independently, plan and prioritize with minimal guidance
• Excellent attention to detail, organization, and communication with varied stakeholders
• Ability to work as a team player with the ability to adapt to changing schedules and assignments
  
  

Travel Requirements

Daily commute to site(s)

Physical Requirements

• Prolonged periods of sitting at a desk and working on a computer, standing and walking.
• Must be able to lift 25 pounds at times.
• Picking, pinching, typing or otherwise working, primarily with fingers rather than with whole hand or arm as in handling.
• Talking: Expressing or exchanging ideas by means of the spoken word; those activities where detailed or important spoken instructions must be conveyed to other workers accurately, loudly, or quickly.
• Hearing: Perceiving the nature of sounds at normal speaking levels with or without correction and having the ability to receive detailed information through oral communication and making fine discriminations in sound.
• The worker is required to have close visual acuity to perform an activity such as: preparing and analyzing data and figures; transcribing; viewing a computer terminal; extensive reading; visual inspection involving small defects, small parts, and/or operation of machines (including inspection); using measurement devices; and/or assembly or fabrication of parts at distances close to the eyes.
  
  

PI270131072

Seniority level

• Seniority level

  Entry level

Employment type

• Employment type

  Full-time

Job function

• Job function

  Research, Analyst, and Information Technology

• Industries

  Hospitals and Health Care

Referrals increase your chances of interviewing at Profound Research by 2x

Get notified about new Clinical Research Coordinator jobs in California, United States.

Associate Clinical Trials Management (Contract)

Redwood City, CA $70,000.00-$90,000.00 5 days ago

Clinical Research Associate I - Heart Institute

Clinical Research Associate I - Heart Institute

Clinical Research Assistant / Emergency Department / Full-time / Days

Clinical Research Associate I - Berman Lab

Clinical Research Coordinator II - 240740

Clinical Research Coord I - Smidt Heart Institute - Makkar Lab

Redwood City, CA $60,000.00-$85,000.00 4 days ago

Clinical Research Associate I - Microbiome Program

Clinical Research Associate I, PER DIEM - Tan Lab

California, United States $19.50-$32.86 2 days ago

Clinical Research Coordinator to Home-Based CRA (Clinical Research Associate) (LA)

We’re unlocking community knowledge in a new way. Experts add insights directly into each article, started with the help of AI.