Haryana Dietitian, clinical i Jobs – 355 Open Jobs Today

Clinical Trial Coordinator
MSD —Gurugram, Haryana
- Full-time
- Research
- Driving
- Travel
5d
Clinical Dietitian
IMedi.Health LLP —Gurugram, Haryana
- ₹25,000 - ₹40,000 a month
- Full-time
- Bachelor's degree
- In-person
Quick apply
2d
Lab Technician
The Orange Health —Gurugram, Haryana
- ₹28,000.03 - ₹30,000.81 a month
- Full-time
- B.Sc
- Laboratory experience
- Bachelor's degree
Quick apply
Clinical Application Specialist - CT
GE HEALTHCARE —Gurugram, Haryana
- English
- Analysis skills
- Bachelor's degree
R&D PDM Associate - Self Care
Reckitt —Gurugram, Haryana
- Doctoral degree
- English
- Master's degree
- Health insurance
R&D Associate, Dettol
Reckitt —Gurugram, Haryana
- Master's degree
- Analysis skills
- Communication skills
- Health insurance
R&D Officer
Reckitt —Gurugram, Haryana
- Engineering
- Microsoft Office
- Master's degree
- Health insurance
Clinical Psychologist
Mental Wellness Centre —Gurugram, Haryana
- ₹40,000 - ₹41,000 a month
- Full-time
- English
- Microsoft Office
- Master's degree
Quick apply
12d
Nursing Tutor
Swami Devi Dyal Group of Professional Institutions, Panchkula —Panchkula, Haryana
- ₹22,000 - ₹25,000 a month
- Nursing
- B.Sc
- Master's degree
Quick apply
Safety & PV Specialist I
サイネオス・ヘルス —Gurugram, Haryana
- Medicine
- B.Sc
- Master's degree
MBBS Physician
Connect and Heal Primary Care Private Limited —Gurugram, Haryana
- ₹8,00,000 - ₹9,00,000 a year
- Full-time
- Medicine
- English
- Bachelor's degree
Quick apply
Formulation Specialist - Toothpaste Formulator
Chipper Consumer Pvt. Ltd. —Gurugram, Haryana
- ₹7,00,000 - ₹10,00,000 a year
- Full-time
- Doctoral degree
- Master's degree
- In-person
Quick apply
R&D Sr. Officer Analytical
Reckitt —Gurugram, Haryana
- Doctoral degree
- Laboratory experience
- Master's degree
- Health insurance
Clinical Dietitian
Ekyana Healthcare Pvt Ltd —Panchkula, Haryana
- ₹15,000 - ₹40,000 a month
- Full-time
- B.Sc
- Master's degree
- Bachelor's degree
Quick apply
10d
Dietitian
Redcliffe labs —Gurgaon H.O, Gurugram, Haryana
- ₹25,000 - ₹35,000 a month
- Full-time
- B.Sc
- Master's degree
- Bachelor's degree
- Health insurance
- Life insurance
Quick apply
Project Leader- Healthcare (MedTech)
Bain & Co. —Gurugram, Haryana
- Full-time
- Microsoft Powerpoint
- Microsoft Excel
- English
Quick apply
2d
Doctor Recruitment – Oscar Super Specialty Hospital & Trauma Centre
Oscar Super Speciality Hospital & Trauma Centre —Charkhi Dadri, Haryana
- ₹3,50,000 - ₹5,00,000 a month
- Full-time
- Medicine
- Bachelor's degree
- In-person
- Cell phone reimbursement
- Food provided
Quick apply
7d
Aesthetic Doctor
KorinMi —Gurugram, Haryana
- ₹4,80,000 - ₹8,40,000 a month
- Full-time
- Medicine
- English
- Bachelor's degree
Quick apply
Head Clinical Research Department
Venus Remedies —Panchkula, Haryana
- Full-time
- Management
- Research
- Project management
Clinical Dietitian
Hobit Technology Pvt.Ltd. —Faridabad, Haryana
- ₹25,000 - ₹28,000 a month
- Full-time
- Master's degree
- Bachelor's degree
- In-person
Quick apply

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Clinical Trial Coordinator

MSD -
Gurugram, Haryana

Apply Now

Job details

Full-time
5 days ago

Qualifications

Clinical research
Research
Driving Licence
Driving

Full job description

Job Description

Clinical Trial Coordinator

Under the oversight of the line-manager, this role is responsible for comprehensive trial and site administration and involves preparing, collating, distributing and archiving clinical documents. The CTC supports clinical supply non-clinical supply management and ensures timely maintenance of tracking and reporting tools, as applicable.
The role is critical to meet planned Site Ready dates, including assisting with the preparation of submission packages to IRB/ERC and Health Authorities. The role will collaborate at local level closely with COM, CRM and CRA. And the person collaborates with finance/budgeting representatives to manage CTRAs and payments.

Responsibilities include, but are not limited to:

Trial and site administration:

o Track (e.g. essential documents) and report (e.g. Safety Reports)
o Ensure collation and distribution of study tools and documents
o Update clinical trial databases (CTMS) and trackers
o Clinical supply non-clinical supply management, in collaboration with other country roles
o Manage Labeling requirements and coordinate/sign translation change request, in collaboration with other country roles (if applicable)

Document management:

o Prepare documents and correspondence
o Collate, distribute/ship, and archive clinical documents, e.g. eTMF
o Assist with eTMF reconciliation
o Execute eTMF Quality Control Plan
o Update manuals/documents (e.g., patient diaries, instructions)
o Document proper destruction of clinical supplies.
o Prepare Investigator trial file binders
o Obtain translations of documents

Regulatory Site Start-Up responsibilities: Collaborate with other country roles to:

o In a timely manner, provide to and collect from investigators forms/lists for site evaluation/validation, site start-up and submissions
o Obtain, track and update study insurance certificates
o Support preparation of submission package for IRB/ERC and support regulatory agencies submissions.
o Publish study results for GCTO and RA where required per local legislation

Budgeting, Agreement and Payments:

Collaborate with finance/budgeting representatives for:
o Develop, control, update and close-out country and site budgets (including Split site budget)
o Develop, negotiate, approve and maintain contracts (e.g. CTRAs)
o Track and report contract negotiations
o Update and maintain contract templates (in cooperation with Legal Department)
o Calculate and execute payments (to investigators, vendors, grants)
o Ensure adherence to financial and compliance procedures
o Monitor and track adherence and disclosures
o Maintain tracking tools
o Obtain and process FCPA documentation in a timely manner

Meeting Planning:
o Organize meetings (create track study memos/letters/protocols)
o Support local investigator meetings (invitations, prepare materials, select venue, support vendor where applicable)

Required Skills:
Adaptability, Best Practices Research, Clinical Research, Clinical Site Management, Clinical Trial Agreements (CTA), Clinical Trial Compliance, Clinical Trial Documentation, Clinical Trial Management, Clinical Trial Planning, Clinical Trials, Clinical Trials Monitoring, Clinical Trials Operations, Cross-Cultural Awareness, Data Archiving, Economic Forecasting, Financial Administration, Financial Forecasting, ICH GCP Guidelines, Legal Archiving, Medical Research, Patient Recruitment, Pharmacovigilance, Regulatory Affairs Compliance, Regulatory Compliance

Preferred Skills:
Current Employees applyHERE

Current Contingent Workers applyHERE

Search Firm Representatives Please Read Carefully
Merck Co., Inc., Rahway, NJ, USA, also known as Merck Sharp Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails.

Employee Status:
Regular

Relocation:
VISA Sponsorship:
Travel Requirements:
Flexible Work Arrangements:
Not Applicable

Shift:
Valid Driving License:
Hazardous Material(s):
Job Posting End Date:
08/26/2026*A job posting is effective until 11:59:59PM on the dayBEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the dayBEFORE the job posting end date.
Requisition ID: R411062

Apply Now

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dietitian, clinical i jobs in haryana

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