ZipRecruiter

Log In

1

Weekend Research Jobs in Michigan (NOW HIRING)

previous pagenext page

Showing results 21-40

All JobsResearch JobsWeekend Research JobsWeekend Research Jobs in Michigan

Weekend Research information

What is a Weekend Research?

A Weekend Research job typically involves conducting research tasks during weekends, which can include data collection, literature reviews, experiments, or analysis depending on the field. These roles are often part-time and may be suited for students, professionals seeking extra income, or those unable to work during regular weekday hours. Weekend research positions can be found in academic institutions, private companies, or independent projects. Responsibilities and requirements vary by employer, but attention to detail, strong organizational skills, and the ability to work independently are usually important.

What are some common challenges faced by Weekend Research professionals, and how can they effectively manage their workload?

Weekend Research professionals often face the challenge of balancing tight deadlines and limited access to colleagues or resources during non-standard hours. To manage these challenges, it’s important to plan tasks ahead, utilize digital collaboration tools, and communicate clearly with team members about progress and needs before the weekend. Additionally, setting clear objectives and prioritizing tasks can help ensure efficient use of time, allowing for thorough and high-quality research even when support is limited.

What are the key skills and qualifications needed to thrive as a Weekend Researcher, and why are they important?

To thrive as a Weekend Researcher, you typically need strong analytical skills, attention to detail, and a relevant academic background or experience in research methods. Familiarity with data analysis tools, online research databases, and citation management systems is often required. Excellent time management, self-motivation, and clear written communication make someone stand out in this position. These skills and qualities are essential for producing accurate, timely, and well-organized research findings, especially within tight weekend deadlines.

What are the most commonly searched types of Research jobs in Michigan?

The most popular types of Research jobs in Michigan are:

What cities in Michigan are hiring for Weekend Research jobs?

Cities in Michigan with the most Weekend Research job openings:

Weekend Research jobs near you
Infographic showing various Weekend Research job openings in Michigan as of August 2026, with employment types broken down into 1% Internship, 1% As Needed, 84% Full Time, 10% Part Time, 1% Temporary, and 3% Contract. Highlights an 85% Physical, 5% Hybrid, and 10% Remote job distribution.

Senior Clinical Research Coordinator

DM Clinical Research

Detroit, MI • On-site

$24 - $32/hr

Full-time

Re-posted 26 days ago

Job description

Senior Clinical Research Coordinator

Department
Clinical Operations - Detroit, MI
Employment Type
Full-Time
Minimum Experience
Experienced
DM Clinical Research, the largest privately-owned research management organization in the Houston area and one of the top 50 in the country, is looking for a Senior Clinical Research Coordinator experienced in coordinating studies for one of our research sites in Detroit, MI. This position works closely with our Clinical Research staff to provide excellent care to patients participating in our clinical trials.
Responsibilities:
  • Completing DMCR-required training, including GCP and IATA.
  • Maintaining a working knowledge of current FDA regulations, GCP/ICH guidelines, organizational SOPs, guidance documents, and study protocols.
  • Adhering to their assigned protocols at their respective site(s).
  • Maintain working knowledge of current FDA GCP/ICH guidelines, organizational SOPs, guidance documents, and study protocols.
  • Collecting source and submitting source per Sponsor requirements via the Sponsor-specified CRF system.
  • Completing Sponsor-required training prior to study-start, to include, but not limited to:
a. Sponsor provided and IRB approved protocol
b. All amendments
c. Investigator Brochure
d. Sponsor-specified EDC and/or IVRS
  • Continued recruitment and screening for their assigned protocols at their respective site(s) at all times as applicable
  • Being prepared for and available at all required company meetings and monitoring visits for their assigned protocols at their respective site(s).
  • Utilizing the most recent version of the Protocol, Informed Consent, and Investigator Brochures at their respective site(s).
  • Compiling and organizing all regulatory and administrative binders for their assigned protocols at their respective site(s) upon initial receipt of and wherever applicable.
  • Creating source documents for their assigned protocols at their respective site(s).
  • Conducting patient visits, and all other protocol-required procedures and documenting these in a timely manner.
  • Reporting all Adverse and Serious Adverse Events to the appropriate authorities per Sponsor, IRB, and ICH Guidelines.
  • Completing data entry and query resolution in a timely manner.
  • Submitting required administrative paperwork per company timelines.
  • Occasionally attending out-of-town Investigator Meetings.
  • Ensuring data quality in all trials being conducted at their respective site(s).
  • Addressing and resolving all issues from that monitor letters for all assigned protocols at their respective site(s) in a timely manner.
  • Striving to meet Sponsor goals for their assigned protocols at their respective site(s).
  • Strive to ensure weekly, monthly, and quarterly assigned goals are met for their respective site(s).
  • Any other matters as assigned by management.

Requirements:
  • Have at least three (5) years of experience as a CRC, preferably with practice coordinating industry sponsored trials in a private setting.
  • Foreign Medical Graduate a plus.
  • Be an energetic, go-getter who is detail-oriented and can multi-task.
  • Be goals-driven while continuously maintaining quality.
  • Have ACRP certification, which is a plus.
  • Bilingual in Spanish is a plus.

Apply