Clinical Research Coordinator Resume Samples - Page 2

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Clinical Research Coordinators manage clinical trials and assess a drug's or medical device benefits and risks. Some usual work duties listed on a Clinical Research Coordinator resume are handling daily activities, interviewing and hiring staff, implementing policies, writing reports, budgeting, and organizing meetings. Qualifications such as healthcare management, financial skills, leadership, analytical thinking and accuracy are often seen on the most successful resume samples. A Bachelor's Degree in a relevant field is required. Ethics and case management expertise are crucial too.

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11

Clinical Research Coordinator

3400 Spruce St., Gates Bldg, 10th Flr, Philadelphia, PA 19104

  • Clinical Research Coordinator
  • Multi-modal study integrating psychosocial, neuropsychological, neuroimaging, and genomics research to identify predictive biomarkers in prodromal/preonset psychosis
  • Conducted semi-structured and structured clinical interviews and computerized neurocognitive battery (CNB) with research participants
  • Wrote and prepared summaries of impressions to be presented at case conference where prodromal status is determined by consensus
Candidate Info
8
years in
workforce
1
year
at this job
HS
High School Diploma
BS
Psychology
Some College
12

Clinical Research Coordinator/r&d Engineer

Responsible for clinical decision-making and regular communication with study subjects and Principal Investigator

  • Assessed clinical performance and ergonomics of devices; provided feedback to multidisciplinary R&D team
  • Maintained detailed logs regarding history of subject participation, employee trainings, device components, etc.
  • Assisted in the development of fail-safe features for new device mechanisms to ensure subject safety
  • Designed procedures for device validation testing including optical, mechanical, electrical, and software
  • Data collection and troubleshooting using various equipment (National Instruments, Thorlabs, Yokogawa, etc.)
  • Assembly and verification of electrical components (prototype breakout boards, cable fabrication, soldering, etc.)
Candidate Info
4
years in
workforce
2
months
at this job
BS
Biomedical Engineering
13

Clinical Research Coordinator

Collaborate with investigators and sponsoring organizations to conduct all aspects of clinical trials

  • Recruited, screened, enrolled, and scheduled study subjects
  • Collected information, recorded all data, completed case report form, and reported SAEs
  • Obtained informed consent, performed assessments, and trained by Canfield medical photography
  • GCP and HIPPA trained, SIVs, interaction and submission to the IRB, study close outs
  • Performed blood draws, specimen shipments, ECGs, vital signs, and ultrasound
  • Attended Investigator Meetings around the US and assigned as Lead Coordinator for clinical trials
Candidate Info
5
years in
workforce
3
years
at this job
BS
Biology
14

Lead Clinical Research Coordinator

CRC for 7 studies; high enroller for 5 of the 7 studies,

  • Worked in a fast paced environment, able to meet deadlines for each database lock
  • Created source documents for studies, performed laboratory processing
  • Conducted and participated in protocol meetings with multidisciplinary staff in attendance
  • Instructed new hires on protocols and on ICH/GCP guidelines
  • Involved in a FDA audit and 2 sponsor audits
  • Interfaced with Sponsors and Monitors
Candidate Info
16
years in
workforce
3
years
at this job
BS
Social Work
MS
Counseling & Personnel Services
15

Clinical Research Coordinator

Oversaw all phases of clinical trials which focused on African Americans and minorities and other urological diseases and conditions

  • Educated community, physicians, and patient care support staff on protocol specifics of clinical trials
  • Managed the community and personal schedules of urologists
  • Served as an liaison with physician and pharmaceutical companies for contract and budget negotiations
  • Credited with coordinating successful health fairs in the Metropolitan Atlanta area with over 1500 participants
  • Facilitated monthly support groups for urological conditions and diseases
  • Managed regulatory documents and clinical trials manuals
Candidate Info
14
years in
workforce
3
years
at this job
BS
Biology
16

Certified Clinical Research Coordinator, Medical Assistant (ob/gyn)

Performed all aspects of project management including subject eligibility, data collection, protocol compliance

  • Assisted physician with all procedures including Physicals, Pap Smears, Endometrial Bxs and Colposcopies
  • Performed lab and specimen submissions
  • Created and redesigned source docs and maintained accurate and complete research files
  • Attended all Investigator Meetings and trainings
  • Performed regulatory submissions, have working knowledge of CFR, GCP and ICH
Candidate Info
15
years in
workforce
9
years
at this job
Medical
17

Clinical Research Coordinator

Submitted start up documents as well as maintained regulatory binders

  • Assisted with budget negotiations and implemented process changes necessary to accommodate new protocols.
  • Scheduled patients and performed patient visits according to protocols and GCP.
  • Performed blood draws, ECG's, and processed blood and urine according to protocol.
  • Entered eCRFs and answered all queries timely.
  • Worked closely with the PI in selection of potential studies and review of ongoing studies.
Candidate Info
28
years in
workforce
5
months
at this job
18

Clinical Research Coordinator

Responsible for enrollment and retention of study subjects

  • Obtained informed consent and medical history
  • Conducted enrollment procedures: Venipuncture, ECG's, Pulmonary Function Tests, vital signs
  • Collected and processed specimens for laboratory evaluation
  • Managed serious adverse event reporting to sponsor and ethics committee
  • Prepared and presented in-services to physicians and study staff
  • Certified Clinical Research Coordinator (CCRC) - March 2012
Candidate Info
9
years in
workforce
2
years
at this job
BS
Human Ecology
19

Clinical Research Coordinator (lead Crc)

Coordinated phase I - IV breast oncology trials (18 active and 7 follow up studies)

  • Worked with monitors during site initiation visits
  • Attended investigator meetings
  • Screened patients in clinic,
  • Performed all required protocol specific procedures, including preparing lab specimens for shipments, shipping labs, data management and preparing for monitor visits.
  • Maintained professional communication with all sponsors Initiated monthly meetings with investigators to review protocols and research patients
  • Managed regulatory, including SAE submissions, advertisement reviews and safety report reviews
Candidate Info
4
years in
workforce
10
months
at this job
AS
Associate of Science
BS
Management
20

Clinical Research Coordinator

Maintained current study progress records and enter clinical data into clinical tracking system.

  • Communicated deviations in study conduct to study team and management.
  • Monitored performance metrics for the trial, observes and reports trends.
  • Facilitated the internal audit plan and process for the trial, ensure adherence to Good Medical
  • Ensured required clinical trial documents (i.e. CV's, lab certifications, financial disclosures, etc.)
  • Assisted with vendor set up and management and assisted in tracking investigational product,
  • Performed site co-monitoring in conformance to all relevant laws, regulations, guidelines and internal SOPs/policies.
  • Carried out 40-50% travel to sites.
Candidate Info
6
years in
workforce
1
year
at this job
HS
Pharmaceutical Medicine
MS
Master of Science
Medicine And Surgery

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