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Weekend Ppd Clinical Research Jobs (NOW HIRING)

Our global Clinical Operations colleagues within our PPD ยฎ clinical research services provide end-to-end support for clinical trials from study start up to monitoring through to study close out ...

Clinical Research Coordinator

Dallas, TX ยท On-site

$24 - $32/hr

Clinical Research Coordinator (Onsite) Dallas, TX Contract Role Ready to make an impact in medical ... Enjoy a steady weekday schedule --no weekends or holidays * Gain hands-on experience with industry ...

Clinical Research Coordinator

Dallas, TX ยท On-site

$24 - $32/hr

Clinical Research Coordinator (Onsite) Dallas, TX Contract Role Ready to make an impact in medical ... Enjoy a steady weekday schedule --no weekends or holidays * Gain hands-on experience with industry ...

Clinical Research Coordinator

Dallas, TX ยท On-site

$24 - $32/hr

Clinical Research Coordinator (Onsite) Dallas, TX Contract Role Ready to make an impact in medical ... Enjoy a steady weekday schedule --no weekends or holidays * Gain hands-on experience with industry ...

Showing results 21-40

Weekend Ppd Clinical Research information

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$8

$22

$46

How much do weekend ppd clinical research jobs pay per hour?

As of Aug 23, 2026, the average hourly pay for weekend ppd clinical research in the United States is $22.71, according to ZipRecruiter salary data. Most workers in this role earn between $17.31 and $25.96 per hour, depending on experience, location, and employer.

What is a Weekend PPD Clinical Research?

A Weekend PPD Clinical Research job involves working primarily on weekends to support clinical research studies managed by PPD, a leading global contract research organization. Employees in this role may assist with tasks such as data collection, patient recruitment, study monitoring, and ensuring compliance with research protocols. This position is ideal for individuals seeking flexible work schedules while contributing to important medical research. Weekend roles are essential for studies that require continuous monitoring or have participants available only outside regular business hours.

What are the key skills and qualifications needed to thrive as a Weekend PPD Clinical Research professional?

To thrive as a Weekend PPD Clinical Research professional, you need a background in life sciences or healthcare, experience in clinical trial processes, and often a relevant degree or certification such as GCP (Good Clinical Practice). Familiarity with electronic data capture (EDC) systems, clinical trial management systems (CTMS), and regulatory documentation is essential for the role. Strong attention to detail, effective communication, and organizational skills set top candidates apart in managing protocol adherence and patient safety. These skills and qualifications ensure high-quality clinical data integrity, compliance with regulations, and smooth trial operations during weekend shifts.

What are some unique challenges and expectations faced by Weekend PPD Clinical Research staff compared to weekday roles?

Weekend PPD Clinical Research staff often work with reduced onsite support and may need to take on a broader range of responsibilities, such as patient monitoring, data entry, and protocol compliance independently. The pace can be variable, with periods of high activity when studies are scheduled and quieter intervals between participant visits. Strong communication skills are essential, as coordination with weekday teams ensures seamless handovers and continuity of care. This role offers valuable experience managing complex clinical tasks autonomously and is ideal for professionals seeking flexible schedules or additional clinical research exposure.

What is the difference between Weekend Ppd Clinical Research vs Clinical Research Coordinator?

AspectWeekend Ppd Clinical ResearchClinical Research Coordinator
CertificationsTypically requires GCP training, CPR, and sometimes clinical research certificationsOften requires GCP training, CPR, and research certifications
Work EnvironmentPart-time, weekend shifts at clinical sites or research facilitiesFull-time or part-time roles at research sites, hospitals, or clinics
Employer & IndustryPharmaceutical companies, CROs, research sitesHospitals, research institutions, pharmaceutical companies

Weekend Ppd Clinical Research roles focus on conducting research activities during weekends, often part-time, while Clinical Research Coordinators manage daily study operations, patient recruitment, and data collection. Both roles require similar certifications but differ mainly in schedule and scope of responsibilities.

What cities are hiring for Weekend Ppd Clinical Research jobs?

Cities with the most Weekend Ppd Clinical Research job openings:

What are the most commonly searched types of Ppd Clinical Research jobs?

The most popular types of Ppd Clinical Research jobs are:

What states have the most Weekend Ppd Clinical Research jobs?

States with the most job openings for Weekend Ppd Clinical Research jobs include:

Clinical Research Coordinator

Flourish Research

Murrieta, CA โ€ข On-site

$31 - $38/hr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 12 days ago


Job description

Valkyrie Clinical Trials, a Flourish Research company, is looking for motivated, talented, creative individuals who want to learn and grow in their careers while contributing to research that changes lives! We offer an excellent comprehensive benefits package, a supportive and collaborative work environment, and endless growth opportunities.
We are actively hiring Clinical Research Coordinators at our Murrieta site location.
The Clinical Research Coordinator assists the Investigators in executing Phase I, II, III, and IV clinical research trials in accordance with Standard Operating Procedures (SOPs), FDA and GCP guidelines, and study protocols while providing an impeccable patient experience in every, single interaction.
Shift:
Monday-Friday, 8:30 AM - 5 PM (occasional weekends)
Location: 25405 Hancock Ave, Suite 110, Murrieta, CA 92562
Compensation: $31.00-$38.00/hr depending on experience
RESPONSIBILITIES

  • Execute protocol-specified patient visits and procedures, which may include, but not limited to, phlebotomy, IVs, injections, vital signs, ECG/EKG, etc.
  • Document assessments and study data per regs/GCP; maintain complete source; accurately complete CRFs/eCRFs.
  • Obtain informed consent per federal regs, GCP, and IRB requirements.
  • Ethically recruit qualified subjects to meet enrollment timelines.
  • Complete required/ongoing training; attend investigator meetings/courses; stay current with changing regulations and Flourish policies.
  • Schedule and conduct visits per protocol timelines.
  • Protect confidentiality per HIPAA and all confidentiality agreements.
  • Report AEs promptly; report SAEs to sponsor within 24 hours and notify PI/Sub-I/supervisor.
  • Account for and ensure availability of trial materials (study drug, labs, CRFs, supplies).
  • Maintain and document communication with Leads, Managers, PIs/Sub-Is, and study team per protocol and policy.
  • Perform duties safely, and in a time-/cost-effective manner compliant with Flourish policies.
  • Represent Flourish professionally in all interactions.
  • Additional duties as assigned by management.

Requirements

  • Bachelor's degree preferred, but not required
  • Must have oncology clinical research experience
  • Minimum of two years of clinical research experience
  • Clinical skills highly preferred: vital signs, EKG/ECG, phlebotomy, and injections
  • Familiar with e-source reporting via an electronic platform
  • A clear understanding of ICH, FDA, and GCP regulations
  • Impeccable organizational skills and attention to detail
  • Excellent communication and interpersonal skills to effectively interact with the Principal Investigator, research team, Study Sponsor/CROs, potential subjects, and referral sources
  • An ethical compass that compels the candidate to be honest, detail-oriented, and self-driven
  • High-level critical thinking skills
  • Working knowledge of medical terminology and lab collection/processing/storage procedures
  • Proficiency with computers and Microsoft Office Suite

Flourish Research offers an excellent comprehensive benefits package, a supportive and collaborative work environment, and endless growth opportunities. Apply today to learn more about how you can join us in our mission to save and improve the lives of others!

Benefits

Health, dental, and vision insurance plans, 401(k) with a 100% employer match on the first 4% of employee contributions, tuition reimbursement, parental leave, referral program, employee assistance program, life insurance, disability insurance, and 15 days of PTO + 8 paid holidays and 2 floating holidays.

Flourish Research is where clinical trials thrive.
Flourish Research is one of the industry’s most progressive and diversified clinical trial organizations, with strong capabilities across cardiology, metabolic disorders, renal, oncology, CNS, pulmonology, and vaccine research.
At Flourish Research, we strive toward excellence. In clinical trials and healthcare, excellence means everyone deserves the best care, regardless of their race, color, gender identity, religion, ethnicity, physical abilities, age, sexual orientation, or veteran status. We embrace employees, customers, and patients from these underrepresented groups to help make this vision a reality.
Flourish Research is driven by a diverse and inclusive community of passionate people who are committed to improving the quality of life of communities around the world. Flourish is committed to a safe work environment where all employees, customers, and patients are included, and treated with dignity and respect.
Flourish Research strives to build an organization that attracts and leverages diversity in our staff, which reflects the diversity of our local communities. We promote education, acceptance, and inclusion because there is beauty in diversity. The more diversity we have in our team, the more unique perspectives, and ideas we share, and the better prepared we are to serve our communities. WE SEE YOU. WE ARE YOU. WE EMBRACE YOU. WE CELEBRATE YOU!
Flourish Research is an equal employment opportunity employer. Employment decisions are based on merit and business needs, and not on race, color, sex, (including pregnancy and gender identity), citizenship status, national origin, ancestry, gender, sexual orientation, age, religion, creed, physical or mental disability, genetic information, marital status, veteran status, political affiliation, or any other factor protected by law. Flourish Research complies with the law regarding reasonable accommodation for handicapped and disabled employees.