Sr Clinical Scientist Job

Rahway NJ
Oct 06, 2016
Oct 21, 2016
Organization Type
Clinical Practice
Sr Clinical Scientist-CLI005305


Merck & Co., Inc. Kenilworth, N.J., U.S.A. known as Merck in the United States and Canada, is a global health care leader with a diversified portfolio of prescription medicines, vaccines and animal health products. Today, we are building a new kind of healthcare company – one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of an individual like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you’ll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


Leads and directs team in key study planning, development and execution elements (e.g., data management deliverables, protocol level plans/timelines, country/site selection, system updates, Investigator Meeting planning and presentations, communication plans, risk identification and mitigation, issue resolution safety and medical monitoring, preparation of status update reports, study closeout activities).


- Facilitates and collaborates with key internal/external stakeholders (trial team, subsidiary country teams, vendors, committees, etc) in support of clinical trial objectives.

- Accountable for managing any trial specific partners and/or vendors.

- Responsible for collaborating wth the Medical Writer on protocol development, clinical study reports, regulatory documents and Study Manager on study deliverables.

- Responsible for regulatory agency update reports, responses to regulatory agencies, and other clinical and regulatory documents.

- Contributes to the authoring of CTD/WMA subsections.

- Supports Clinical Directors in scientific leadership/investigator initiatives including preparation of publications, meeting presentations, etc.


Education Minimum Requirements:

- Degree in the Life Sciences or significant experience in clinical development (> 11 years).

- Bachelor’s degree with 7+ years’; or MS with 5+ years’; or PhD with

- Pharmaceutical and/or clinical drug development experience.

- Excellent oral (including presentation) and written communication, computer/ database management and project management skills.

Required Experience and Skills:

- Understanding scientific process, as well as medical and statistical concepts.

- Understanding of all aspects of clinical development from program planning to regulatory submission.

- Ability to contribute and collaborate with a team including proactive issue identification and resolution. Must be able to make independent, timely, data-driven and appropriate decisions.

- Must have excellent, demonstrated oral (including presentation) and written communication, and computer/database management skills.

- Demonstrated project management skills with proven ability to lead cross-functional team and individuals.

- Ability to influence and collaborate internally as well as externally with partners and study-related vendors.

Preferred Experience and Skills:

- Minimum 3 years’ experience in Infectious Diseases areas of pharmaceutical industry preferable. Medical writing experience a plus.

Our employees are the key to our company’s success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Our Company’s benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. If you need an accommodation for the application process please email us at

Search Firm Representatives Please Read Carefully:

Merck & Co., Inc. is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

For more information about personal rights under Equal Employment Opportunity, visit:

EEOC Poster

EEOC GINA Supplement​

Merck is an equal opportunity employer, Minority/Female/Disability/Veteran – proudly embracing diversity in all of its manifestations.

Job: Clinical Research - Clin Ops

Job Title:Sr. Scientist, Clin. Operations

Primary Location: NA-US-NJ-Rahway

Other Locations: NA-US-PA-Upper Gwynedd

Employee Status: Regular

Travel: Yes, 15 % of the Time

Number of Openings: 3

Shift (if applicable): 1st

Hazardous Materials: None

Company Trade Name:Merck