Clinical Operations Manager

SmartRecruiters, Inc.

Fort Lee (NJ)

On-site

USD 61,000 - 87,000

Full time

3 days ago
Be an early applicant
Application generator

Get a reply from this recruiter — a resume and cover letter tailored to exactly what they’re hiring for.

Get past ATS filters

Job summary

Global Channel Management is seeking an experienced healthcare/clinical trial professional to oversee multiple studies, including global programs. The role requires strong communication with vendors and peers, deep knowledge of the trial lifecycle, and the ability to manage protocol development, feasibility, and reporting with minimal supervision.

The ideal candidate has a bachelor's degree and at least 3 years in healthcare or clinical trials, plus a solid grasp of GCPs and regulatory

Qualifications

  • Bachelor's degree and minimum 3 years experience in the healthcare or clinical trial industry, or the equivalent combination of education and experience.
  • Extensive knowledge of clinical development principles, theories and concepts and high degree of comprehension of pharmaceutical industry practices, standards and GCPs.
  • Thorough working knowledge of the clinical trial lifecycle from protocol development and feasibility through study closeout and reporting.
  • Ability to manage complex, multiple studies simultaneously, some of which may be global in scope.
  • Excellent written and oral communication skills and ability to communicate in medical and scientific terms with vendors, consultants, and peers.
  • Ability to read, analyze and interpret professional journals, technical procedures and government regulations; ability to write reports, business correspondence and procedures.
  • Ability to solve problems and deal effectively with a variety of variables in situations of limited standardization.
  • Must be tactful, mature, flexible and have well developed interpersonal skills, able to work independently and in a team, multi-task and prioritize to complete assignments.

Responsibilities

  • Manage complex, multiple studies simultaneously, some of which may be global in scope.
  • Communicate effectively with vendors, consultants, and peers in medical and scientific terms.
  • Read, analyze and interpret professional journals, technical procedures and government regulations; write reports and procedures.
  • Coach and develop direct report(s) and manage the efforts of team members.
  • Coordinate with internal stakeholders to ensure timelines, budgets, and quality controls are met.

Skills

Clinical trials
Communication
Multi-tasking
Vendor coordination
GCP knowledge

Education

Bachelor's degree

Job description

Global Channel Management is a technology company that specializes in various types of recruiting and staff augmentation. Our account managers and recruiters have over a decade of experience in various verticals. GCM understands the challenges companies face when it comes to the skills and experience needed to fill the void of the day to day function. Organizations need to reduce training and labor costs but at same requiring the best "talent " for the job.

Qualifications

Bachelor's
degree and minimum 3 years experience in the healthcare or clinical
trial industry, or the equivalent combination of education and
experience.

Extensive
knowledge of clinical development principles, theories and concepts and
high degree of comprehension of pharmaceutical industry practices,
standards and GCP's.

Thorough
working knowledge of the clinical trial lifecycle from protocol
development and feasibility through study closeout and reporting.

Ability to manage complex, multiple studies simultaneously. Some may be of a global nature.

Excellent
written and oral communication skills. Ability to communicate in
medical and scientific terms with vendors, consultants, and peers.

Ability
to read analyze and interpret professional journals, technical
procedures and or government regulations. Ability to write reports,
business correspondence and procedures .

Ability to solve problems and deal effectively with a variety of variables in situations of limited standardization.

Must
be tactful, mature, flexible and have well developed interpersonal
skills, able to work independently and in a team, multi-task and
prioritize in order to complete assignments on time, coach and manage
the efforts and development of direct report(s). .

Additional Information

$54/hr

12 months

By clicking the link above or any third-party link within this posting, you are leaving this site and going to a third-party website where the third-party website's terms and privacy policy apply

Get your free, confidential resume review.

or drag and drop your file here.

Similar jobs

Similar jobs worth comparing

Clinical Trials Manager
Clinical Trials Manager

SmartRecruiters, Inc. • Fort Lee (NJ)

On-site
USD 61,000 - 87,000
Clinician
Clinician

SmartRecruiters, Inc. • South San Francisco (CA)

On-site
USD 52,000 - 62,000
Global Trial Manager
Global Trial Manager

SmartRecruiters, Inc. • South San Francisco (CA)

On-site
USD 61,000 - 87,000
Clinical Trials Manager
Clinical Trials Manager

SmartRecruiters, Inc. • Marlborough (MA)

On-site
USD 96,000 - 124,000
Clinical Study Manager
Clinical Study Manager

SmartRecruiters, Inc. • New York (NY)

On-site
USD 80,000 - 113,000
Clinical Research Scientist
Clinical Research Scientist

SmartRecruiters, Inc. • Madison (NJ)

On-site
USD 68,000 - 97,000
Competitive pay
Clinical Scientist
Clinical Scientist

SmartRecruiters, Inc. • Pearl River (NY)

On-site
USD 60,000 - 68,000
Clinical Study Manager
Clinical Study Manager

SmartRecruiters, Inc. • Parsippany-Troy Hills (NJ)

On-site
USD 34,000 - 49,000
Clinical Study Manager
Clinical Study Manager

SmartRecruiters, Inc. • Bernards Township (NJ)

On-site
USD 66,000 - 91,000
$57/hr
6 months
MC Clinical Applications Coordinator
MC Clinical Applications Coordinator

SmartRecruiters, Inc. • Woonsocket (RI)

On-site
USD 120,000 - 132,000