Skip to content
CV Rocket
Get started
How it worksThe enginePricingBlogContactSign in

Open nowPosted 4222 days ago

Clinical Scientist

Integrated Resources INC628 open roles

Where
Collegeville, PA, United States
Work mode
On site
Get the CV for this job

From $25 per CV, paid once. No subscription.

Your applicationOpen nowClinical ScientistIntegrated Resources INC · Collegeville, PA, United States

  1. YouYes, apply to this one.

  2. CV RocketCV written for this posting.

  3. 25 readersRecruiter, hiring manager, skeptic. Round after round.

  4. CV RocketApplied on Integrated Resources INC's own form.

The reply lands in your private mailbox

3×more interviews than doing it yourself with ChatGPT.

The clock on this job

Early applications get read.

8.0% of postings close within 7 days. Measured by our own scanner across the market.

Share of postings closed within
  1. 1.6%1 day
  2. 3.6%3 days
  3. 8.0%7 days
  4. 15.0%14 days
  5. 34.2%30 days
This job: posted 4222 days ago

The posting

Company Description

A Few Words About Us Integrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well-respected professional specialty firms. IRI has built its reputation on excellent service and integrity since its inception in 1996. Our mission centers on delivering only the best quality talent, the first time and every time. We provide quality resources in four specialty areas: Information Technology (IT), Clinical Research, Rehabilitation Therapy and Nursing.

Job Description

RESPONSIBILITIES:

• The Supporting Clinician will provide medical and scientific study and project support for multiple, global, Phase 1-4 clinical studies in a clinical program.

• coordinating and leading the investigation process on all manufacturing and laboratory incidents related to all deviations including biomanufacturing process and equipment deviations and deviations for all analytical assays.

• protocol and study training

• Data review and interpretation

• study and/or program scientific and integrity oversight

• safety review and communication

• regulatory document, study report and publication preparation and review

• Independently write/design protocol outlines, protocols, and amendments of moderate complexity in collaboration with the Lead Clinician

• Support the preparation of other clinical documents as required

• DATA REVIEW AND INTERPRETATION:

o Proactively coordinate with the Lead Clinician to assure understanding and agreement on deliverables

o Responsible for review of patient level data across a study and coordinating with Lead Clinician for study level review as delegated

o Study analysis and decision point preparation

o Interprets data and is able to identify issues of moderate/difficult complexity

o Conducts data review independently

• STUDY MEDICAL OVERSIGHT:

o Collaborates with the Lead Study Clinician(s) and COSTL to provide guidance during the execution of the study

o Provide input into the monitoring plan

• SAFETY:

o Ensure timely communication of safety issues

o Review and approval of subject narratives as delegated by the Lead Clinician

• REGULATORY AND PUBLICATIONS:

o Provide input, review and edit clinical study reports (CSR)

o Provide full review of content and integrates information from literature and other sources as appropriate

o Support and contribute to various sections of regulatory filings (Pediatric Investigational Plan, IB, IND/NDA Annual Reports, and PSURs and Regulatory authority responses)

o Audit responses as delegated by the Lead Clinician

• CLINICAL PROGRAM IMPLEMENTATION:

o Ensure regulatory compliance and GCP adherence at the study level with regard to medical/scientific issues

o Initiate and coordinate corrective action for major medical/safety/scientific study level issues

o Along with Lead Study Clinician(s) and COSTL and with regard to medical/safety concerns, ensures study level issues are resolved

o Collaborate with Lead Clinician and COSTL to arrive at major site level decisions based on input from the team

o Coordinates with Lead Study Clinician(s) and COSTL to maintain study timelines

o Along with the Lead Study Clinician(s) and COSTL and other study team members, participates in training of Study Management Staff and monitoring staff

o In collaboration with the Lead Study Clinician(s) and COSTL and study team, ensures the clinical trial material requirements of the study are met

o Ensure standard processes, tools, and procedures used consistently and globally

o Participates in developing training strategy for study with the study team members

Provide input into the preparation of study level training materials in collaboration with Lead Study Clinician(s) and COSTL and team members

o Ensures appropriate filing of documentation in the trial master file

Qualifications

QUALIFICATIONS AND SKILLS NEEDED:

• M.D., PhD, Pharm. D. Degree in science or health-related field preferred, will consider highly motivated and experienced MA or MS

• 10+ years of pharmaceutical/CRO experience preferred

TECHNICAL SKILLS:

• Has extensive knowledge of the clinical research process and Good Clinical Practices from previous employment experience in the clinical research field

• Has demonstrated ability and level of experience with integrating and summarizing medical/scientific concepts in protocols and other clinical documents

• Has independently authored clinical study documents

• Has experience with participating in and informally leading an operational team

• Applies knowledge of internal/external business challenges to facilitate process improvements

• Has ability to proactively resolve issues and work independently with minimal supervision

• Has working knowledge of statistics, data analysis, and data interpretation

• Has exceptional written and oral communication and cross-functional collaborative skills

• Is proficient in MS Word, Excel, and PowerPoint

From $25, paid onceGet the CV for this job

What happens when you press

One press. We do the rest.

  1. A CV for this posting

    Written against Integrated Resources INC's own wording, from every piece of relevant proof in your profile.

  2. 25 readers review it

    Recruiter, hiring manager, skeptic and more read every draft, round after round. You get the best round.

    The review screen in CV Rocket: how each CV was read, round by round.

  3. We apply on Integrated Resources INC's form

    Our application engine gets through the hardest forms there are. Where a question needs you, AI suggests the best answer. Don't want us applying from our IP addresses? Use our Chrome extension: we apply straight from your own browser.

    An application in CV Rocket: every answer filled in on the employer's form.

  4. Every reply, sorted

    Integrated Resources INC's answer lands in your private mailbox, and we classify it on arrival: interview, question, rejection.

    The CV Rocket inbox: each employer reply classified as an interview, an action or a rejection.

  5. Reply with AI

    AI helps you write the email, checks it and sends it. We show you whether the recruiter read it.

  6. The interview in your calendar

    Full integration with your calendar. The invitation goes straight in.

    An interview invitation in the CV Rocket inbox, added to the candidate's calendar.
Get the CV for this job

From $25 per CV, paid once. No subscription.

Why it works

3×

more interviews than doing it yourself with ChatGPT.

ChatGPT writes a CV and never learns what happened to it. We see every reply. For each CV we know:

  • How it was written, and how the review scored it
  • When we applied, and how long after the posting went up
  • Which posting, which company, which city
  • Who got the interview, and who heard nothing

That is how we know which CVs get called.

Get the CV for this job

From $25 per CV, paid once. No subscription.

The numbers game

More applications. More interviews.

Every application goes out with its own CV, written for that posting and paid once. Send enough of them and the law of large numbers finds you the job.

Get the CV for this job
By hand5–10
With CV Rocket100
applications a day

Nearby

Live postings like this one

Same employer first, then the same role elsewhere.

Before you press

Straight answers

Get the CV for this job

From $25 per CV, paid once. No subscription.

What if my background isn't good enough?

We make the most of the background you have. The CV uses every piece of relevant proof your profile holds, and one of the 25 readers reads your whole profile and flags what the CV left out.

Do you really apply for me?

Yes, on the employer's own form, the hardest ones included. Where a question needs you, you answer it right there and AI suggests the best answer. Don't want us applying from our IP addresses? Use our Chrome extension: we apply straight from your own browser.

Is it a subscription?

No. You pay once per CV, from $25. Every application goes out with its own CV, written for that posting.

One job. One CV.
Paid once.

Pick the posting you want. We write for it, apply for you and catch the reply.

Get the CV for this job

From $25 per CV, paid once. No subscription.